Recent progress in asymmetric Biginelli reaction

The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1 )-ones) are interesting materials due to their significant pharmacologi...

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Published inMolecular diversity Vol. 17; no. 2; pp. 389 - 407
Main Authors Heravi, Majid M., Asadi, Shima, Lashkariani, Boshra Malekzadeh
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.05.2013
Springer Nature B.V
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Online AccessGet full text
ISSN1381-1991
1573-501X
1573-501X
DOI10.1007/s11030-013-9439-9

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Abstract The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1 )-ones) are interesting materials due to their significant pharmacological and structural profiles. In the last decades, the asymmetric synthesis as a powerful tool has an effective impact on the Biginelli products and has increased their potencies and applications as drugs. Having the importance of this subject in mind, in this review we wish to present the recent rapid progress of asymmetric Biginelli reaction.
AbstractList The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1 )-ones) are interesting materials due to their significant pharmacological and structural profiles. In the last decades, the asymmetric synthesis as a powerful tool has an effective impact on the Biginelli products and has increased their potencies and applications as drugs. Having the importance of this subject in mind, in this review we wish to present the recent rapid progress of asymmetric Biginelli reaction.
(ProQuest: ... denotes formulae and/or non-USASCII text omitted; see image) The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1...)-ones) are interesting materials due to their significant pharmacological and structural profiles. In the last decades, the asymmetric synthesis as a powerful tool has an effective impact on the Biginelli products and has increased their potencies and applications as drugs. Having the importance of this subject in mind, in this review we wish to present the recent rapid progress of asymmetric Biginelli reaction.[PUBLICATION ABSTRACT]
The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1H)-ones) are interesting materials due to their significant pharmacological and structural profiles. In the last decades, the asymmetric synthesis as a powerful tool has an effective impact on the Biginelli products and has increased their potencies and applications as drugs. Having the importance of this subject in mind, in this review we wish to present the recent rapid progress of asymmetric Biginelli reaction.
The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1H)-ones) are interesting materials due to their significant pharmacological and structural profiles. In the last decades, the asymmetric synthesis as a powerful tool has an effective impact on the Biginelli products and has increased their potencies and applications as drugs. Having the importance of this subject in mind, in this review we wish to present the recent rapid progress of asymmetric Biginelli reaction.The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1H)-ones) are interesting materials due to their significant pharmacological and structural profiles. In the last decades, the asymmetric synthesis as a powerful tool has an effective impact on the Biginelli products and has increased their potencies and applications as drugs. Having the importance of this subject in mind, in this review we wish to present the recent rapid progress of asymmetric Biginelli reaction.
Author Heravi, Majid M.
Asadi, Shima
Lashkariani, Boshra Malekzadeh
Author_xml – sequence: 1
  givenname: Majid M.
  surname: Heravi
  fullname: Heravi, Majid M.
  email: mmh1331@yahoo.com
  organization: Department of Chemistry, School of Sciences, Alzahra University
– sequence: 2
  givenname: Shima
  surname: Asadi
  fullname: Asadi, Shima
  organization: Department of Chemistry, School of Sciences, Alzahra University
– sequence: 3
  givenname: Boshra Malekzadeh
  surname: Lashkariani
  fullname: Lashkariani, Boshra Malekzadeh
  organization: Department of Chemistry, School of Sciences, Alzahra University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23588897$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1021/ja056092f
10.1021/jm990202+
10.1021/jm990612y
10.1074/jbc.M606192200
10.1039/c0ob01268h
10.1021/jo060339p
10.1002/ejoc.201000894
10.1016/S1074-5521(02)00212-0
10.1021/jo0624187
10.5012/jkcs.2009.53.1.090
10.1021/jm00130a029
10.1055/s-0029-1217710
10.1021/ja905320q
10.1016/S0968-0896(00)82188-4
10.2174/157017911795529218
10.1021/jo101717m
10.1126/science.1077215
10.1016/j.tet.2012.07.027
10.1080/17518250802342527
10.1523/JNEUROSCI.3345-09.2009
10.1016/S0960-894X(99)00227-9
10.1039/c2cs15361k
10.1016/j.molcata.2005.08.009
10.1002/ejoc.200900455
10.1080/00397911003668596
10.1021/jm990200p
10.1016/S1872-2067(11)60377-X
10.1021/jo01104a629
10.1016/S0960-894X(99)00653-8
10.1016/j.tetlet.2008.03.080
10.1038/nchembio.2007.10
10.1021/bi026716j
10.1021/jo801463j
10.2174/157017810791824919
10.5012/bkcs.2011.32.2.656
10.1002/adsc.200900597
10.1016/0223-5234(96)85874-0
10.1002/ejoc.201000448
10.1590/S0103-50532004000200002
10.1007/s11030-008-9094-8
10.1002/cjoc.200890392
10.1002/chem.200700840
10.1039/a903712h
10.1016/S0223-5234(00)01189-2
10.1039/b309910e
10.1080/10426509608029657
10.1002/qsar.200320001
10.1126/science.286.5441.971
10.3998/ark.5550190.0009.606
10.1002/kin.550050102
10.1070/RC1978v047n07ABEH002243
10.1021/ol051476w
10.1016/j.ejmech.2006.09.003
10.1016/j.bmcl.2007.11.027
10.1016/j.catcom.2005.12.007
10.1055/s-2002-20956
10.1016/j.tetasy.2007.03.002
10.1021/jm981114c
10.1016/j.bmcl.2007.01.111
10.1016/j.tetasy.2012.10.002
10.1134/S107042720605017X
10.1021/jm9902032
10.1021/jm00171a044
10.2174/138527211793797837
10.1016/j.molcata.2005.04.033
10.1074/jbc.M404857200
10.1021/jo060064d
10.1016/S0960-894X(00)00374-7
10.1016/S0960-894X(01)80810-6
10.1021/jo000711f
10.1039/b504256a
10.4314/bcse.v23i1.21312
10.1016/j.tetasy.2006.01.034
10.4314/bcse.v25i2.65910
10.1039/b212239a
10.1002/ejoc.200801046
10.1021/ol0614727
10.1016/j.tet.2007.11.044
10.1039/b514296m
10.1002/chem.200701581
10.1002/anie.200500297
10.1021/ja065267y
10.1021/jm990201h
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Thu Apr 24 23:08:58 EDT 2025
Tue Jul 01 00:49:10 EDT 2025
Fri Feb 21 02:33:51 EST 2025
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Dihydropyrimidin-2
Asymmetric synthesis
Biginelli
Multicomponent reactions (MCRs)
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References Khaleghi, Heravi, Khosroshahi, Behbahani, Daroogheha (CR10) 2008; 1
Grekov, Veselov (CR78) 1978; 47
Fina, Edwards (CR79) 1973; 5
Westermann, Neuhaus (CR89) 2005; 44
Aron, Overman (CR34) 2004; 2004
Kappe (CR15) 2000; 35
Deres, Schröder, Paessens, Goldmann, Hacker, Weber, Krämer, Niewöhner, Pleiss, Stoltefuss, Graef, Koletzki, Masantschek, Reimann, Jaeger, Groß, Beckermann, Schlemmer, Haebich (CR31) 2003; 299
Huang, Yang (CR61) 2005; 127
Xu, Li, Wang (CR64) 2012; 68
Lagu, Tian, Chiu, Nagarathnam, Fang, Shen, Forray, Ransom, Chang, Vyas, Zhang, Gluchowski (CR28) 2000; 10
Hinman (CR81) 1958; 23
Mossé, Alexakis (CR90) 2006; 8
Lagu, Tian, Nagarathnam, Marzabadi, Wong, Miao, Zhang, Sun, Chiu, Fang, Forray, Chang, Ransom, Chen, O’Malley, Zhang, Vyas, Gluchowski (CR26) 1999; 42
Kappe (CR2) 2003; 22
Heys, Moore, Murphy (CR32) 2000; 29
CR33
Rodina, Vilenchik, Moulick, Aguirre, Kim, Chiang, Litz, Clement, Kang, She, Wu, Felts, Wipf, Massague, Jiang, Brodsky, Krystal, Chiosis (CR46) 2007; 3
de Graaff, Ruijter, Orru (CR55) 2012; 41
Nagarathnam, Miao, Lagu, Chiu, Fang, Zhang, Tyagarajan, Marzabadi, Zhang, Wong, Sun, Tian, Wetzel, Forray, Chang, Broten, Ransom, Schorn, Chen, O’Malley, Kling, Schneck, Bendesky, Harrell, Vyas, Gluchowski (CR24) 1999; 42
Wisen, Androsavich, Evans, Chang, Gestwicki (CR43) 2008; 18
Ding, Zhao (CR60) 2010; 2010
González-Olvera, Demare, Regla, Juaristi (CR67) 2008; 2008
CR70
Heravi, Asadi (CR58) 2012; 23
Russowsky, Lopes, da Silva, Canto, Godói (CR38) 2004; 15
Lemay, Ogilvie (CR84) 2005; 7
Chen, Xu, Liu, Cun, Gong (CR74) 2006; 128
Ghorab, Mohamed, Mohamed, Ammar (CR49) 1996; 108
Barrow, Nantermet, Selnick, Glass, Rittle, Gilbert, Steele, Homnick, Freidinger, Ransom, Kling, Reiss, Broten, Schorn, Chang, O’Malley, Olah, Ellis, Barrish, Kassahun, Leppert, Nagarathnam, Forray (CR42) 2000; 43
Wang, Yu, Miao, Chen (CR69) 2011; 9
Rodríguez, Bolm (CR88) 2006; 71
Barrow, Glass, Selnick, Freidinger, Chang, O’Malley, Woyden (CR29) 2000; 10
Tao, He, Sun, Kou (CR93) 2005; 2005
Ashok, Holla, Kumari (CR50) 2007; 42
Yadav, Rai, Rai, Awasthi (CR92) 2008; 64
Li, Lu, Huang, Ma, Sun, Wang, Pan (CR77) 2010; 7
Gong, Chen, Xu (CR57) 2007; 13
Hekmatshoar, Heidari, Heravi, Baghernejad (CR5) 2011; 25
Atwal, Rovnyak, Kimball, Floyd, Moreland, Swanson, Gougoutas, Schwartz, Smillie, Malley (CR20) 1990; 33
CR87
Tajbakhsh, Mohajerani, Heravi, Ahmadi (CR13) 2005; 236
Kappe (CR16) 2005
Magerramov, Kurbanova, Abdinbekova, Rzaeva, Farzaliev, Allakhverdiev (CR51) 2006; 79
Fleming (CR80) 1977
Murali Dhar, Nagarathnam, Marzabadi, Lagu, Wong, Chiu, Tyagarajan, Miao, Zhang, Sun, Tian, Shen, Zhang, Wetzel, Forray, Chang, Broten, Schorn, Chen, O’Malley, Ransom, Schneck, Bendesky, Harrell, Vyas, Zhang, Gilbert, Pettibone, Patane, Bock, Freidinger, Gluchowski (CR25) 1999; 42
CR82
Atwal, Moreland (CR21) 1991; 1
Zeinali-Dastmalbaf, Davoodnia, Heravi, Tavakoli-Hoseini, Khojastehnezhad, Zamani (CR14) 2011; 32
Wichmann, Adam, Kolczewski, Mutel, Woltering (CR52) 1999; 9
Hosseini, Stiasni, Barbieri, Kappe (CR91) 2007; 72
Zhu, Cun, Mi, Jiang, Gong (CR71) 2006; 17
Alajarin, Vaquero, Alvarez-Builla, Sunkel, Priego, Gomez-Sal, Torres (CR22) 1994; 2
Fewell, Smith, Lyon, Dumitrescu, Wipf, Day, Brodsky (CR45) 2004; 279
Li, Chen, Song, Luo, Fan, Gong (CR62) 2009; 131
Saha, Moorthy (CR65) 2011; 76
Guillena, Ramón, Yus (CR56) 2007; 18
Wang, Yu, Miao, Chena (CR68) 2009; 351
Goss, Schaus (CR95) 2008; 73
Xin, Chang, Hou, Shang, Liu, Feng (CR73) 2008; 14
Li, Chen, Liu, Xia, Wang (CR75) 2011; 15
Lemay, Ogilvie (CR83) 2006; 71
Ahn, Shin, Jun, Jung, Kang, Kim, Rhee, Kang, Kim, Sohn, Kim, Jin, Lee, Cheon, Kim (CR85) 2007; 17
Jinwal, Miyata, Koren, Jones, Trotter, Chang, O’Leary, Morgan, Lee, Shults, Rousaki, Weeber, Zuiderweg, Gestwicki, Dickey (CR44) 2009; 29
Matache, Dobrota, Bogdan, Funeriu (CR54) 2011; 8
Heravi, Behbahani, Zadsirjan, Oskooie (CR8) 2006; 12
Schleifer (CR23) 1999; 42
Heravi, Behbahani, Oskooie (CR7) 2008; 26
Ranu, Hajra, Jana (CR39) 2000; 65
Bozsing, Sohar, Gigler, Kovacs (CR48) 1996; 31
Li, Chen, Song, Luo, Fan, Gong (CR94) 2009; 131
Mayer, Kapoor, Haggarty, King, Schreiber, Mitchison (CR30) 1999; 286
Huang, Yang, Zhu (CR63) 2005; 127
Sohn, Lee, Joung, Lee (CR66) 2009; 2009
Suzuki, Iwata, Takeda (CR86) 2008; 49
Maliga, Kapoor, Mitchison (CR40) 2002; 9
Oskooie, Heravi, Karimi, Monjezy (CR12) 2011; 41
Cho, Ueda, Shima, Mizuno, Hayashimatsu, Ohnaka, Takeuchi, Hamaguchi, Aisaka (CR19) 1989; 32
Lu, Bai (CR36) 2002; 4
Hekmatshoar, Heidari, Heravi, Baghernejad (CR3) 2009; 23
Moghaddas, Davoodnia, Heravi, Tavakoli-Hoseini (CR11) 2012; 33
Evans, Wisen, Gestwicki (CR47) 2006; 281
Wong, Sun, Lagu, Tian, Marzabadi, Zhang, Nagarathnam, Miao, Wetzel, Peng, Forray, Chang, Chen, Ransom, O’Malley, Broten, Kling, Vyas, Zhang, Gluchowski (CR27) 1999; 42
Kastron, Vitolin, Khanina, Duburs, Kimenis (CR18) 1987; 21
Varala, Mujahid, Adapa (CR37) 2003; 1
DeBonis, Simorre, Crevel, Lebeau, Skoufias, Blangy, Ebel, Gans, Cross, Hackney, Wade, Kozielski (CR41) 2003; 42
Khanina, Siliniece, Ozols, Duburs, Kimenis (CR17) 1978; 12
Heravi, Bakhtiari, Bamoharram (CR6) 2006; 7
Cai, Yang, Li, Jiang, Lai, Jiang, Xu (CR59) 2010; 2010
Chowdari, Ramachary, Barbas (CR72) 2003; 5
Hekmatshoar, Heidari, Heravi, Baghernejad (CR4) 2009; 53
Biginelli (CR1) 1893; 23
Kolosov, Orlov, Beloborodov, Dotsenko (CR35) 2009; 13
Suresh, Sandhu (CR53) 2012; 1
Li, Chen, Wang, Pan (CR76) 2009; 2009
Heravi, Derikvand, Bamoharram (CR9) 2005; 242
ZD Aron (9439_CR34) 2004; 2004
ZY Li (9439_CR77) 2010; 7
EL Khanina (9439_CR17) 1978; 12
BC Ranu (9439_CR39) 2000; 65
I Suzuki (9439_CR86) 2008; 49
B Lagu (9439_CR28) 2000; 10
M Matache (9439_CR54) 2011; 8
J Lu (9439_CR36) 2002; 4
MM Heravi (9439_CR58) 2012; 23
G-H Tao (9439_CR93) 2005; 2005
R Hinman (9439_CR81) 1958; 23
N Li (9439_CR94) 2009; 131
MA Kolosov (9439_CR35) 2009; 13
AM Magerramov (9439_CR51) 2006; 79
D Russowsky (9439_CR38) 2004; 15
MM Heravi (9439_CR7) 2008; 26
UK Jinwal (9439_CR44) 2009; 29
9439_CR82
M Tajbakhsh (9439_CR13) 2005; 236
R González-Olvera (9439_CR67) 2008; 2008
MM Heravi (9439_CR9) 2005; 242
CG Evans (9439_CR47) 2006; 281
ZY Li (9439_CR76) 2009; 2009
LZ Gong (9439_CR57) 2007; 13
9439_CR89
Y-F Cai (9439_CR59) 2010; 2010
9439_CR87
JC Barrow (9439_CR29) 2000; 10
S Saha (9439_CR65) 2011; 76
R Hekmatshoar (9439_CR3) 2009; 23
CO Kappe (9439_CR16) 2005
KS Atwal (9439_CR21) 1991; 1
L Heys (9439_CR32) 2000; 29
H Cho (9439_CR19) 1989; 32
B Rodríguez (9439_CR88) 2006; 71
M Hosseini (9439_CR91) 2007; 72
9439_CR70
9439_CR71
A Rodina (9439_CR46) 2007; 3
C Graaff de (9439_CR55) 2012; 41
CO Kappe (9439_CR15) 2000; 35
Y Huang (9439_CR61) 2005; 127
JHC Sohn (9439_CR66) 2009; 2009
D-Z Xu (9439_CR64) 2012; 68
9439_CR33
9439_CR74
9439_CR72
N Li (9439_CR62) 2009; 131
9439_CR73
D Bozsing (9439_CR48) 1996; 31
I Fleming (9439_CR80) 1977
JC Barrow (9439_CR42) 2000; 43
S Khaleghi (9439_CR10) 2008; 1
9439_CR25
WC Wong (9439_CR27) 1999; 42
TU Mayer (9439_CR30) 1999; 286
MM Ghorab (9439_CR49) 1996; 108
K Deres (9439_CR31) 2003; 299
S DeBonis (9439_CR41) 2003; 42
J Wichmann (9439_CR52) 1999; 9
D Ding (9439_CR60) 2010; 2010
S Wisen (9439_CR43) 2008; 18
Z-Y Li (9439_CR75) 2011; 15
HA Oskooie (9439_CR12) 2011; 41
M Lemay (9439_CR84) 2005; 7
M Zeinali-Dastmalbaf (9439_CR14) 2011; 32
Z Maliga (9439_CR40) 2002; 9
Y Huang (9439_CR63) 2005; 127
SW Fewell (9439_CR45) 2004; 279
YY Wang (9439_CR68) 2009; 351
AP Grekov (9439_CR78) 1978; 47
KS Atwal (9439_CR20) 1990; 33
M Moghaddas (9439_CR11) 2012; 33
R Varala (9439_CR37) 2003; 1
R Hekmatshoar (9439_CR4) 2009; 53
MM Heravi (9439_CR6) 2006; 7
R Alajarin (9439_CR22) 1994; 2
VV Kastron (9439_CR18) 1987; 21
JM Goss (9439_CR95) 2008; 73
NJ Fina (9439_CR79) 1973; 5
B Lagu (9439_CR26) 1999; 42
CO Kappe (9439_CR2) 2003; 22
JH Ahn (9439_CR85) 2007; 17
Y Wang (9439_CR69) 2011; 9
M Ashok (9439_CR50) 2007; 42
9439_CR92
R Hekmatshoar (9439_CR5) 2011; 25
9439_CR90
D Nagarathnam (9439_CR24) 1999; 42
G Guillena (9439_CR56) 2007; 18
M Lemay (9439_CR83) 2006; 71
P Biginelli (9439_CR1) 1893; 23
K-J Schleifer (9439_CR23) 1999; 42
MM Heravi (9439_CR8) 2006; 12
Suresh (9439_CR53) 2012; 1
2391701 - J Med Chem. 1990 Sep;33(9):2629-35
21192642 - J Org Chem. 2011 Jan 21;76(2):396-402
10579841 - J Med Chem. 1999 Nov 18;42(23):4778-93
17331715 - Bioorg Med Chem Lett. 2007 May 1;17(9):2622-8
14740029 - Chem Commun (Camb). 2004 Feb 7;(3):253-65
15912549 - Angew Chem Int Ed Engl. 2005 Jun 27;44(26):4077-9
10987417 - Bioorg Med Chem Lett. 2000 Sep 4;10(17):1917-20
17070617 - Eur J Med Chem. 2007 Mar;42(3):380-5
10673105 - Bioorg Med Chem Lett. 2000 Jan 17;10(2):175-8
16010324 - Chem Commun (Camb). 2005 Jul 28;(28):3562-4
10579843 - J Med Chem. 1999 Nov 18;42(23):4804-13
11248403 - Eur J Med Chem. 2000 Dec;35(12 ):1043-52
12574631 - Science. 2003 Feb 7;299(5608):893-6
19793966 - J Neurosci. 2009 Sep 30;29(39):12079-88
10987976 - J Org Chem. 2000 Sep 22;65(19):6270-2
12703794 - Chem Commun (Camb). 2003 Mar 21;(6):728-9
10579842 - J Med Chem. 1999 Nov 18;42(23):4794-803
19082754 - Mol Divers. 2009 Feb;13(1):5-25
16305212 - J Am Chem Soc. 2005 Nov 30;127(47):16386-7
10893308 - J Med Chem. 2000 Jul 13;43(14):2703-18
21394354 - Org Biomol Chem. 2011 Apr 21;9(8):3050-4
15448148 - J Biol Chem. 2004 Dec 3;279(49):51131-40
18767801 - J Org Chem. 2008 Oct 3;73(19):7651-6
16973602 - J Biol Chem. 2006 Nov 3;281(44):33182-91
22546840 - Chem Soc Rev. 2012 May 21;41(10):3969-4009
10542155 - Science. 1999 Oct 29;286(5441):971-4
17105279 - J Am Chem Soc. 2006 Nov 22;128(46):14802-3
10579840 - J Med Chem. 1999 Nov 18;42(23):4764-77
12525161 - Biochemistry. 2003 Jan 21;42(2):338-49
18060774 - Bioorg Med Chem Lett. 2008 Jan 1;18(1):60-5
21188287 - European J Org Chem. 2010 Jul 1;2010(20):3802-3805
16869664 - Org Lett. 2006 Aug 3;8(16):3577-80
2552119 - J Med Chem. 1989 Oct;32(10):2399-406
10377225 - J Med Chem. 1999 Jun 17;42(12):2204-11
16479280 - Chem Commun (Camb). 2006 Feb 28;(8):819-24
17288387 - J Org Chem. 2007 Feb 16;72(4):1417-24
16146372 - Org Lett. 2005 Sep 15;7(19):4141-4
7922143 - Bioorg Med Chem. 1994 May;2(5):323-9
10386938 - Bioorg Med Chem Lett. 1999 Jun 7;9(11):1573-6
16555849 - J Org Chem. 2006 Mar 31;71(7):2888-91
17603540 - Nat Chem Biol. 2007 Aug;3(8):498-507
18246559 - Chemistry. 2008;14(10):3177-81
16749802 - J Org Chem. 2006 Jun 9;71(12):4663-6
19785440 - J Am Chem Soc. 2009 Oct 28;131(42):15301-10
12323373 - Chem Biol. 2002 Sep;9(9):989-96
12735752 - Org Lett. 2003 May 15;5(10):1685-8
17828720 - Chemistry. 2007;13(32):8920-6
References_xml – volume: 1
  start-page: 67
  year: 2003
  end-page: 70
  ident: CR37
  article-title: Bismuth triflate catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2 (1 )-ones: an improved protocol for the Biginelli reaction
  publication-title: Synlett
– volume: 1
  start-page: 66
  year: 2012
  end-page: 133
  ident: CR53
  article-title: Past, present and future of the Biginelli reaction: a critical perspective
  publication-title: Arkivoc
– volume: 127
  start-page: 16386
  year: 2005
  end-page: 16387
  ident: CR63
  article-title: Highly enantioseletive Biginelli reaction using a new chiral ytterbium catalyst:asymmetric synthesis of dihydropyrimidines
  publication-title: J Am Chem Soc
  doi: 10.1021/ja056092f
– ident: CR70
– volume: 42
  start-page: 4794
  year: 1999
  end-page: 4803
  ident: CR26
  article-title: Design and synthesis of novel 1a adrenoceptor-selective antagonists. 3. Approaches to eliminate opioid agonist metabolites by using substituted phenylpiperazine side chains
  publication-title: J Med Chem
  doi: 10.1021/jm990202+
– volume: 12
  start-page: 369
  year: 2006
  end-page: 372
  ident: CR8
  article-title: Iron (III) phosphate dihydrate—catalyzed one-pot synthesis of dihydropyrimidinones and thiones: an improved procedure for the Biginelli reaction
  publication-title: Heterocycl Commun
– volume: 44
  start-page: 4077
  year: 2005
  end-page: 4079
  ident: CR89
  article-title: Dihydroxyacetone in amino acid catalyzed Mannich-type reactions
  publication-title: Angew Chem Int Ed
– volume: 23
  start-page: 141
  year: 2009
  end-page: 144
  ident: CR3
  article-title: Efficient sodium selenate-catalyzed synthesis of 3,4-dihydro-2(1 )- pyrimidinones and -thiones under solvent-free conditions
  publication-title: Bull Chem Soc Ethiop
– volume: 17
  start-page: 491
  year: 2006
  end-page: 493
  ident: CR71
  article-title: A highly enantioselective organocatalyst for the Michael addition of cyclic ketones to nitroolefins
  publication-title: Tetrahedron: Asymmetry
– volume: 5
  start-page: 1685
  year: 2003
  end-page: 1688
  ident: CR72
  article-title: Organocatalytic asymmetric assembly reactions: one-pot synthesis of functionalized $$\beta $$ -amino alcohols from aldehydes, ketones, and azodicarboxylates
  publication-title: Org Lett
– volume: 43
  start-page: 2703
  year: 2000
  end-page: 2718
  ident: CR42
  article-title: In vitro and in vivo evaluation of dihydropyrimidinone -5 amides as potent and selective 1a receptor antagonists for the treatment of benign prostatic hyperplasia
  publication-title: J Med Chem
  doi: 10.1021/jm990612y
– volume: 281
  start-page: 33182
  year: 2006
  end-page: 33191
  ident: CR47
  article-title: Heat Shock Proteins 70 and 90 inhibit early stages of amyloid B-(1–42) aggregation in vitro
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M606192200
– volume: 9
  start-page: 3050
  year: 2011
  end-page: 3054
  ident: CR69
  article-title: Bifunctional primary amine-thiourea-TfOH (BPAT TfOH) as a chiral phase-transfer catalyst: the asymmetric synthesis of dihydropyrimidines
  publication-title: Org Biomol Chem
  doi: 10.1039/c0ob01268h
– volume: 71
  start-page: 4663
  year: 2006
  end-page: 4666
  ident: CR83
  article-title: Mechanistic studies of hydrazide-catalyzed enantioselective Diels–Alder reactions
  publication-title: J Org Chem
  doi: 10.1021/jo060339p
– volume: 42
  start-page: 4778
  year: 1999
  end-page: 4793
  ident: CR25
  article-title: Design and synthesis of novel $$\alpha $$ 1a adrenoceptor-selective antagonists. 2. Approaches to eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety 1,2
  publication-title: J Med Chem
– volume: 2010
  start-page: 4986
  year: 2010
  end-page: 4990
  ident: CR59
  article-title: Cooperative and enantioselective NbCl /primary amine catalyzed Biginelli reaction
  publication-title: Eur J Org Chem
  doi: 10.1002/ejoc.201000894
– ident: CR87
– volume: 9
  start-page: 989
  year: 2002
  end-page: 996
  ident: CR40
  article-title: Evidence that monastrol is an allosteric inhibitor of the mitotic kinesin Eg5
  publication-title: Chem Biol
  doi: 10.1016/S1074-5521(02)00212-0
– volume: 72
  start-page: 1417
  year: 2007
  end-page: 1424
  ident: CR91
  article-title: Microwave-assisted asymmetric organocatalysis. A probe for nonthermal microwave effects and the concept of simultaneous cooling
  publication-title: J Org Chem
  doi: 10.1021/jo0624187
– volume: 53
  start-page: 90
  year: 2009
  end-page: 94
  ident: CR4
  article-title: NiSO 7H O: an efficient and eco-friendly catalyst for the one-pot synthesis of dihydropyrimidin-2(1 )-ones
  publication-title: J Korean Chem Soc
  doi: 10.5012/jkcs.2009.53.1.090
– volume: 32
  start-page: 2399
  year: 1989
  end-page: 2406
  ident: CR19
  article-title: Dihydropyrimidines: novel calcium antagonists with potent and long-lasting vasodilative and anti-hypertensive activity
  publication-title: J Med Chem
  doi: 10.1021/jm00130a029
– volume: 23
  start-page: 360
  year: 1893
  end-page: 413
  ident: CR1
  article-title: Aldehyde-urea derivatives of aceto and oxaloacetic acids
  publication-title: Gazz Chim Ital
– volume: 2009
  start-page: 2356
  year: 2009
  end-page: 2360
  ident: CR76
  article-title: Highly enantioselective direct aldol reactions catalyzed by proline derivatives based on a calix[4]arene scaffold in the presence of water
  publication-title: Synlett
  doi: 10.1055/s-0029-1217710
– volume: 131
  start-page: 15301
  year: 2009
  end-page: 15310
  ident: CR62
  article-title: Highly enantioselective organocatalytic Biginelli and Biginelli-like condensations: reversal of the stereochemistry by tuning the 3,3 -disubstituents of phosphoric acids
  publication-title: J Am Chem Soc
  doi: 10.1021/ja905320q
– volume: 2
  start-page: 323
  year: 1994
  end-page: 329
  ident: CR22
  article-title: Imidazo[1,5-a]pyrimidine and benzo[4,5]imidazo[1,2-a]pyrimidine derivatives as calcium antagonists
  publication-title: Bioorg Med Chem
  doi: 10.1016/S0968-0896(00)82188-4
– volume: 8
  start-page: 356
  year: 2011
  end-page: 373
  ident: CR54
  article-title: Recent developments in the reactivity of the Biginelli compounds
  publication-title: Curr Org Synth
  doi: 10.2174/157017911795529218
– volume: 76
  start-page: 396
  year: 2011
  end-page: 402
  ident: CR65
  article-title: Enantioselective organocatalytic Biginelli reaction: dependence of the catalyst on sterics, hydrogen bonding, and reinforced chirality
  publication-title: J Org Chem
  doi: 10.1021/jo101717m
– volume: 299
  start-page: 893
  year: 2003
  end-page: 896
  ident: CR31
  article-title: Inhibition of hepatitis B virus replication by drug-induced depletion of nucleocapsids
  publication-title: Science
  doi: 10.1126/science.1077215
– volume: 68
  start-page: 7867
  year: 2012
  end-page: 7872
  ident: CR64
  article-title: Highly enantioselective Biginelli reaction catalyzed by a simple chiral primary amine catalyst: asymmetric synthesis of dihydropyrimidines
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2012.07.027
– volume: 1
  start-page: 133
  year: 2008
  end-page: 139
  ident: CR10
  article-title: A very high yielding and facile alkaline earth metals homogeneous catalysis of Biginelli reaction: an improved protocol
  publication-title: Green Chem Lett Rev
  doi: 10.1080/17518250802342527
– volume: 29
  start-page: 12079
  year: 2009
  end-page: 12088
  ident: CR44
  article-title: Chemical manipulation of Hsp70 ATPase activity regulates Tau stability
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.3345-09.2009
– year: 2005
  ident: CR16
  publication-title: Multicomponent reactions
– volume: 9
  start-page: 1573
  year: 1999
  end-page: 1576
  ident: CR52
  article-title: Structure-activity relationships of substituted 5 -thiazolo[3,2-a]pyrimidines as group 2 metabotropic glutamate receptor antagonists
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(99)00227-9
– volume: 41
  start-page: 3969
  year: 2012
  end-page: 4009
  ident: CR55
  article-title: Recent developments in asymmetric multicomponent reactions
  publication-title: Chem Soc Rev
  doi: 10.1039/c2cs15361k
– volume: 242
  start-page: 173
  year: 2005
  end-page: 175
  ident: CR9
  article-title: A catalytic method for synthesis of Biginelli-type 3,4-dihydropyrimidin-2 (1 )-one using 12-tungstophosphoric acid
  publication-title: J Mol Catal A
  doi: 10.1016/j.molcata.2005.08.009
– volume: 2009
  start-page: 3858
  year: 2009
  end-page: 3862
  ident: CR66
  article-title: Probing the mode of asymmetric induction of Biginelli reaction using proline ester salts
  publication-title: Eur J Org Chem
  doi: 10.1002/ejoc.200900455
– volume: 41
  start-page: 826
  year: 2011
  end-page: 831
  ident: CR12
  article-title: FeCl immobilized in Al-MCM 41: an efficient catalyst system for the Biginelli reaction
  publication-title: Synth Commun
  doi: 10.1080/00397911003668596
– volume: 42
  start-page: 4764
  year: 1999
  end-page: 4777
  ident: CR24
  article-title: Design and synthesis of novel 1a adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones
  publication-title: J Med Chem
  doi: 10.1021/jm990200p
– volume: 33
  start-page: 706
  year: 2012
  end-page: 710
  ident: CR11
  article-title: Sulfonated carbon catalyzed Biginelli reaction for one-pot synthesis of 3,4-dihydropyrimidin-2(1 )-ones and -thiones
  publication-title: Chin J Catal
  doi: 10.1016/S1872-2067(11)60377-X
– volume: 127
  start-page: 16386
  year: 2005
  end-page: 16387
  ident: CR61
  article-title: Highly enantioseletive Biginelli reaction using a new chiral ytterbium catalyst? asymmetric synthesis of dihydropyrimidines
  publication-title: J Am Chem Soc
  doi: 10.1021/ja056092f
– volume: 23
  start-page: 1587
  year: 1958
  end-page: 1588
  ident: CR81
  article-title: Notes-base strengths of some alkylhydrazines
  publication-title: J Org Chem
  doi: 10.1021/jo01104a629
– volume: 10
  start-page: 175
  year: 2000
  end-page: 178
  ident: CR28
  article-title: Synthesis and evaluation of furo[3,4-d]pyrimidinones as selective 1a-adrenergic receptor antagonists
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(99)00653-8
– volume: 49
  start-page: 3238
  year: 2008
  end-page: 3241
  ident: CR86
  article-title: Biginelli reactions catalyzed by hydrazine type organocatalyst
  publication-title: Tetrahedron Lett
  doi: 10.1016/j.tetlet.2008.03.080
– volume: 3
  start-page: 498
  year: 2007
  end-page: 507
  ident: CR46
  article-title: Selective compounds define Hsp90 as a major inhibitor of apoptosis in small-cell lung cancer
  publication-title: Nat Chem Biol
  doi: 10.1038/nchembio.2007.10
– volume: 42
  start-page: 338
  year: 2003
  end-page: 349
  ident: CR41
  article-title: Interaction of the mitotic inhibitor Monastrol with human kinesin Eg5
  publication-title: Biochem
  doi: 10.1021/bi026716j
– volume: 73
  start-page: 7651
  year: 2008
  end-page: 7656
  ident: CR95
  article-title: Enantioselective synthesis of SNAP-7941: chiral dihydropyrimidone inhibitor of MCH1-R
  publication-title: J Org Chem
  doi: 10.1021/jo801463j
– volume: 7
  start-page: 461
  year: 2010
  end-page: 466
  ident: CR77
  article-title: Novel prolinamide organocatalysts based on calix[4]arene scaffold for the enantioselective direct aldol reaction
  publication-title: Lett Org Chem
  doi: 10.2174/157017810791824919
– volume: 32
  start-page: 656
  year: 2011
  end-page: 658
  ident: CR14
  article-title: Silica gel-supported polyphosphoric acid (PPA-SiO ) catalyzed one-pot multi-component synthesis of 3,4-dihydropyrimidin-2(1 )-ones and -thiones: an efficient method for the Biginelli reaction
  publication-title: Bull Korean Chem Soc
  doi: 10.5012/bkcs.2011.32.2.656
– volume: 351
  start-page: 3057
  year: 2009
  end-page: 3062
  ident: CR68
  article-title: Highly enantioselective Biginelli reaction promoted by chiral bifunctional primary amine-thiourea catalysts: asymmetric synthesis of dihydropyrimidines
  publication-title: Adv Synth Catal
  doi: 10.1002/adsc.200900597
– volume: 31
  start-page: 663
  year: 1996
  end-page: 668
  ident: CR48
  article-title: Synthesis and pharmacological study of new 3,4-dihydro-2 ,6 -pyrimido-[2,1-b][l,3]thiazines
  publication-title: Eur J Med Chem
  doi: 10.1016/0223-5234(96)85874-0
– volume: 2010
  start-page: 3802
  year: 2010
  end-page: 3805
  ident: CR60
  article-title: Primary amine-catalyzed Biginelli reaction for the enantioselective synthesis of 3,4-dihydropyrimidin-2(1 )-ones
  publication-title: Eur J Org Chem
  doi: 10.1002/ejoc.201000448
– volume: 12
  start-page: 72
  year: 1978
  end-page: 74
  ident: CR17
  article-title: Synthesis and pharmacological studies of some 1,2,3,4-tetrahydropyrimidine-5-carboxylic acid derivatives
  publication-title: Khim Farm Zh
– volume: 15
  start-page: 165
  year: 2004
  end-page: 169
  ident: CR38
  article-title: Multicomponent Biginelli’s synthesis of 3,4-dihydropyrimidin-2(1 )-ones promoted by SnCl$_2\cdot 2 _2$O
  publication-title: J Braz Chem Soc
  doi: 10.1590/S0103-50532004000200002
– volume: 13
  start-page: 5
  year: 2009
  end-page: 25
  ident: CR35
  article-title: A chemical placebo: NaCl as an effective, cheapest, non-acidic and greener catalyst for Biginelli-type 3,4-dihydropyrimidin-2(1 )-ones (-thiones) synthesis
  publication-title: Mol Divers
  doi: 10.1007/s11030-008-9094-8
– volume: 131
  start-page: 15301
  year: 2009
  end-page: 15310
  ident: CR94
  article-title: Highly enantioselective organocatalytic Biginelli and Biginelli-like condensations: reversal of the stereochemistry by tuning the 3,3 -disubstituents of phosphoric acids
  publication-title: J Am Chem Soc
  doi: 10.1021/ja905320q
– volume: 26
  start-page: 2203
  year: 2008
  end-page: 2206
  ident: CR7
  article-title: Ferric perchlorate catalyzed one-pot synthesis of 1,2,3,4-tetrahydro-2-pyrimidinones and -thiones: an expedient protocol for the Biginelli reaction
  publication-title: Chin J Chem
  doi: 10.1002/cjoc.200890392
– volume: 13
  start-page: 8920
  year: 2007
  end-page: 8926
  ident: CR57
  article-title: Asymmetric organocatalytic Biginelli reactions: a new approach to quickly access optically active 3,4-dihydropyrimidin-2-(1 )-ones
  publication-title: Chem Eur J
  doi: 10.1002/chem.200700840
– volume: 29
  start-page: 57
  year: 2000
  end-page: 67
  ident: CR32
  article-title: The guanidine metabolites of Ptilocaulisspiculifer and related compounds; isolation and synthesis
  publication-title: Chem Soc Rev
  doi: 10.1039/a903712h
– volume: 35
  start-page: 1043
  year: 2000
  end-page: 1052
  ident: CR15
  article-title: Biologically active dihydropyrimidones of the Biginelli-type—a literature survey
  publication-title: Eur J Med Chem
  doi: 10.1016/S0223-5234(00)01189-2
– ident: CR33
– volume: 2004
  start-page: 253
  year: 2004
  end-page: 265
  ident: CR34
  article-title: The tethered Biginelli condensation in natural product synthesis
  publication-title: Chem Commun
  doi: 10.1039/b309910e
– volume: 108
  start-page: 249
  year: 1996
  end-page: 256
  ident: CR49
  article-title: Synthesis and radiation stability of novel thiazolopyrimidines with expected antifungal activity
  publication-title: Phosphorus Sulfur
  doi: 10.1080/10426509608029657
– ident: CR82
– volume: 22
  start-page: 630
  year: 2003
  end-page: 645
  ident: CR2
  article-title: The generation of dihydropyrimidine libraries utilizing Biginelli multicomponent chemistry
  publication-title: QSAR Comb Sci
  doi: 10.1002/qsar.200320001
– volume: 286
  start-page: 971
  year: 1999
  end-page: 974
  ident: CR30
  article-title: Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen
  publication-title: Science
  doi: 10.1126/science.286.5441.971
– volume: 2008
  start-page: 61
  year: 2008
  end-page: 72
  ident: CR67
  article-title: Application of (1S,4S)-2,5-diazabicyclo[2.2.1]heptane derivatives in asymmetric organocatalysis: the Biginelli reaction
  publication-title: Arkivoc
  doi: 10.3998/ark.5550190.0009.606
– volume: 5
  start-page: 1
  year: 1973
  end-page: 26
  ident: CR79
  article-title: The alpha effect. A review
  publication-title: Int J Chem Kinet
  doi: 10.1002/kin.550050102
– volume: 8
  start-page: 3577
  year: 2006
  end-page: 3580
  ident: CR90
  article-title: Organocatalyzed asymmetric reactions via microwave activation
  publication-title: Org Lett
– volume: 14
  start-page: 3177
  year: 2008
  end-page: 3181
  ident: CR73
  article-title: An Enantioselective Biginelli reaction catalyzed by a simple chiral secondary amine and achiral brønsted acid by a dual- activation route
  publication-title: Chem Eur J
– volume: 47
  start-page: 631
  year: 1978
  end-page: 648
  ident: CR78
  article-title: The -effect in the chemistry of organic compounds
  publication-title: Russ Chem Rev
  doi: 10.1070/RC1978v047n07ABEH002243
– volume: 7
  start-page: 4141
  year: 2005
  end-page: 4144
  ident: CR84
  article-title: Aqueous enantioselective organocatalytic Diels–Alder reactions employing hydrazide catalysts. A new scaffold for organic acceleration
  publication-title: Org Lett
  doi: 10.1021/ol051476w
– volume: 42
  start-page: 380
  year: 2007
  end-page: 385
  ident: CR50
  article-title: Convenient one pot synthesis of some novel derivatives of thiazolo[2,3-b]dihydropyrimidinone possessing 4-methylthiophenyl moiety and evaluation of their antibacterial and antifungal activities
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2006.09.003
– volume: 18
  start-page: 60
  year: 2008
  end-page: 65
  ident: CR43
  article-title: Chemical modulators of heat shock protein 70 (Hsp70) by sequential, microwaveaccelerated reactions on solid phase
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2007.11.027
– volume: 7
  start-page: 373
  year: 2006
  end-page: 376
  ident: CR6
  article-title: 12-Molybdophosphoric acid: a recyclable catalyst for the synthesis of Biginelli-type 3,4-dihydropyrimidine-2(1 )-ones
  publication-title: Catal Commun
  doi: 10.1016/j.catcom.2005.12.007
– volume: 4
  start-page: 466
  year: 2002
  end-page: 470
  ident: CR36
  article-title: Catalysis of the Biginelli reaction by ferric and nickel chloride hexahydrates. One-pot synthesis of 3,4-dihydropyrimidin-2(1 )-ones
  publication-title: Synthesis
  doi: 10.1055/s-2002-20956
– volume: 18
  start-page: 693
  year: 2007
  end-page: 700
  ident: CR56
  article-title: Organocatalytic enantioselective multicomponent reactions (OEMCRs)
  publication-title: Tetrahedron Asymmetry
  doi: 10.1016/j.tetasy.2007.03.002
– volume: 25
  start-page: 309
  year: 2011
  end-page: 313
  ident: CR5
  article-title: Mesoporous molecular sieve MCM-41 catalyzed one-pot synthesis of 3,4-dihydro-2(1 )-pyrimidinones and -thiones under solvent-free conditions
  publication-title: Bull Chem Soc Ethiop
– volume: 42
  start-page: 2204
  year: 1999
  end-page: 2211
  ident: CR23
  article-title: Stereoselective characterization of the 1,4-dihydropyridine binding site at L-type calcium channels in the resting state and the opened/inactivated state
  publication-title: J Med Chem
  doi: 10.1021/jm981114c
– volume: 17
  start-page: 2622
  year: 2007
  end-page: 2628
  ident: CR85
  article-title: Synthesis, biological evaluation and structural determination of -aminoacyl-containing cyclic hydrazine derivatives as dipeptidyl peptidase IV (DPP-IV) inhibitors
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmcl.2007.01.111
– volume: 23
  start-page: 1431
  year: 2012
  end-page: 1465
  ident: CR58
  article-title: Recent applications of organocatalysts in asymmetric aldol reactions
  publication-title: Tetrahedron Asymmetry
  doi: 10.1016/j.tetasy.2012.10.002
– volume: 79
  start-page: 787
  year: 2006
  end-page: 790
  ident: CR51
  article-title: Synthesis and antioxidative properties of some 3,4-dihydropyrimidin-2(1 )ones(-thiones)
  publication-title: Russ J Appl Chem
  doi: 10.1134/S107042720605017X
– volume: 42
  start-page: 4804
  year: 1999
  end-page: 4813
  ident: CR27
  article-title: Design and synthesis of novel 1a adrenoceptor-selective antagonists. 4. Structure-activity relationship in the dihydropyrimidine series
  publication-title: J Med Chem
  doi: 10.1021/jm9902032
– volume: 64
  start-page: 1420
  year: 2008
  end-page: 1429
  ident: CR92
  article-title: Chiral ionic liquid-catalyzed Biginelli reaction: stereoselective synthesis of polyfunctionalized perhydropyrimidines
  publication-title: Tetrahedron
– volume: 33
  start-page: 2629
  year: 1990
  end-page: 2635
  ident: CR20
  article-title: Dihydropyrimidine calcium channel blockers. II. 3-Substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines
  publication-title: J Med Chem
  doi: 10.1021/jm00171a044
– volume: 15
  start-page: 39
  year: 2011
  end-page: 61
  ident: CR75
  article-title: The use of calixarenes in asymmetric catalysis
  publication-title: Curr Org Chem
  doi: 10.2174/138527211793797837
– volume: 236
  start-page: 216
  year: 2005
  end-page: 219
  ident: CR13
  article-title: Natural HEU type zeolite catalyzed Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1 ) one derivatives
  publication-title: J Mol Catal A
  doi: 10.1016/j.molcata.2005.04.033
– volume: 279
  start-page: 51131
  year: 2004
  end-page: 51140
  ident: CR45
  article-title: Small molecule modulators of endogenous and cochaperone stimulated Hsp70 ATPase activity
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M404857200
– volume: 128
  start-page: 14802
  year: 2006
  end-page: 14803
  ident: CR74
  article-title: Highly enantioselective organocatalytic Biginelli reaction
  publication-title: J Am Chem Soc
– volume: 71
  start-page: 2888
  year: 2006
  end-page: 2891
  ident: CR88
  article-title: Thermal effects in the organocatalytic asymmetric Mannich reaction
  publication-title: J Org Chem
  doi: 10.1021/jo060064d
– volume: 21
  start-page: 948
  year: 1987
  end-page: 952
  ident: CR18
  article-title: Fluorine-containing derivatives of 1,2,3,4-tetrahydropyrimidine: synthesis and pharmacological activity
  publication-title: Khim Farm Zh
– volume: 10
  start-page: 1917
  year: 2000
  end-page: 1920
  ident: CR29
  article-title: Preparation and evaluation of 1,3-diaminocyclopentane-linked dihydropyrimidinone derivatives as selective 1a-receptor antagonists
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(00)00374-7
– volume: 1
  start-page: 291
  year: 1991
  end-page: 294
  ident: CR21
  article-title: Dihydropyrimidine calcium channel blockers 51: bicyclic dihydropyrimidines as potent mimics of dihydropyridines
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(01)80810-6
– volume: 65
  start-page: 6270
  year: 2000
  end-page: 6272
  ident: CR39
  article-title: Indium (III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes, and urea: an improved procedure for the Biginelli reaction
  publication-title: J Org Chem
  doi: 10.1021/jo000711f
– year: 1977
  ident: CR80
  publication-title: Frontier orbitals and organic chemical reactions
– volume: 2005
  start-page: 3562
  year: 2005
  end-page: 3564
  ident: CR93
  article-title: New generation ionic liquids: Cations derived from amino acids
  publication-title: Chem Commun
  doi: 10.1039/b504256a
– volume: 42
  start-page: 4764
  year: 1999
  ident: 9439_CR24
  publication-title: J Med Chem
  doi: 10.1021/jm990200p
– volume: 299
  start-page: 893
  year: 2003
  ident: 9439_CR31
  publication-title: Science
  doi: 10.1126/science.1077215
– ident: 9439_CR33
– volume: 4
  start-page: 466
  year: 2002
  ident: 9439_CR36
  publication-title: Synthesis
  doi: 10.1055/s-2002-20956
– volume: 42
  start-page: 338
  year: 2003
  ident: 9439_CR41
  publication-title: Biochem
  doi: 10.1021/bi026716j
– volume: 281
  start-page: 33182
  year: 2006
  ident: 9439_CR47
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M606192200
– volume: 23
  start-page: 141
  year: 2009
  ident: 9439_CR3
  publication-title: Bull Chem Soc Ethiop
  doi: 10.4314/bcse.v23i1.21312
– volume: 22
  start-page: 630
  year: 2003
  ident: 9439_CR2
  publication-title: QSAR Comb Sci
  doi: 10.1002/qsar.200320001
– volume: 131
  start-page: 15301
  year: 2009
  ident: 9439_CR94
  publication-title: J Am Chem Soc
  doi: 10.1021/ja905320q
– ident: 9439_CR71
  doi: 10.1016/j.tetasy.2006.01.034
– volume: 23
  start-page: 360
  year: 1893
  ident: 9439_CR1
  publication-title: Gazz Chim Ital
– volume: 9
  start-page: 3050
  year: 2011
  ident: 9439_CR69
  publication-title: Org Biomol Chem
  doi: 10.1039/c0ob01268h
– volume: 25
  start-page: 309
  year: 2011
  ident: 9439_CR5
  publication-title: Bull Chem Soc Ethiop
  doi: 10.4314/bcse.v25i2.65910
– volume: 242
  start-page: 173
  year: 2005
  ident: 9439_CR9
  publication-title: J Mol Catal A
  doi: 10.1016/j.molcata.2005.08.009
– volume: 35
  start-page: 1043
  year: 2000
  ident: 9439_CR15
  publication-title: Eur J Med Chem
  doi: 10.1016/S0223-5234(00)01189-2
– ident: 9439_CR82
  doi: 10.1039/b212239a
– volume: 3
  start-page: 498
  year: 2007
  ident: 9439_CR46
  publication-title: Nat Chem Biol
  doi: 10.1038/nchembio.2007.10
– volume: 49
  start-page: 3238
  year: 2008
  ident: 9439_CR86
  publication-title: Tetrahedron Lett
  doi: 10.1016/j.tetlet.2008.03.080
– volume: 71
  start-page: 2888
  year: 2006
  ident: 9439_CR88
  publication-title: J Org Chem
  doi: 10.1021/jo060064d
– volume: 2010
  start-page: 4986
  year: 2010
  ident: 9439_CR59
  publication-title: Eur J Org Chem
  doi: 10.1002/ejoc.201000894
– volume: 12
  start-page: 369
  year: 2006
  ident: 9439_CR8
  publication-title: Heterocycl Commun
– volume: 32
  start-page: 2399
  year: 1989
  ident: 9439_CR19
  publication-title: J Med Chem
  doi: 10.1021/jm00130a029
– ident: 9439_CR87
  doi: 10.1002/ejoc.200801046
– ident: 9439_CR90
  doi: 10.1021/ol0614727
– volume: 76
  start-page: 396
  year: 2011
  ident: 9439_CR65
  publication-title: J Org Chem
  doi: 10.1021/jo101717m
– volume: 7
  start-page: 461
  year: 2010
  ident: 9439_CR77
  publication-title: Lett Org Chem
  doi: 10.2174/157017810791824919
– volume: 2005
  start-page: 3562
  year: 2005
  ident: 9439_CR93
  publication-title: Chem Commun
  doi: 10.1039/b504256a
– volume: 13
  start-page: 5
  year: 2009
  ident: 9439_CR35
  publication-title: Mol Divers
  doi: 10.1007/s11030-008-9094-8
– volume: 15
  start-page: 165
  year: 2004
  ident: 9439_CR38
  publication-title: J Braz Chem Soc
  doi: 10.1590/S0103-50532004000200002
– volume: 29
  start-page: 12079
  year: 2009
  ident: 9439_CR44
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.3345-09.2009
– ident: 9439_CR92
  doi: 10.1016/j.tet.2007.11.044
– volume: 13
  start-page: 8920
  year: 2007
  ident: 9439_CR57
  publication-title: Chem Eur J
  doi: 10.1002/chem.200700840
– volume: 31
  start-page: 663
  year: 1996
  ident: 9439_CR48
  publication-title: Eur J Med Chem
  doi: 10.1016/0223-5234(96)85874-0
– volume: 21
  start-page: 948
  year: 1987
  ident: 9439_CR18
  publication-title: Khim Farm Zh
– ident: 9439_CR70
  doi: 10.1039/b514296m
– volume: 23
  start-page: 1431
  year: 2012
  ident: 9439_CR58
  publication-title: Tetrahedron Asymmetry
  doi: 10.1016/j.tetasy.2012.10.002
– volume: 42
  start-page: 4804
  year: 1999
  ident: 9439_CR27
  publication-title: J Med Chem
  doi: 10.1021/jm9902032
– ident: 9439_CR73
  doi: 10.1002/chem.200701581
– volume: 33
  start-page: 706
  year: 2012
  ident: 9439_CR11
  publication-title: Chin J Catal
  doi: 10.1016/S1872-2067(11)60377-X
– volume: 1
  start-page: 133
  year: 2008
  ident: 9439_CR10
  publication-title: Green Chem Lett Rev
  doi: 10.1080/17518250802342527
– volume: 108
  start-page: 249
  year: 1996
  ident: 9439_CR49
  publication-title: Phosphorus Sulfur
  doi: 10.1080/10426509608029657
– volume: 79
  start-page: 787
  year: 2006
  ident: 9439_CR51
  publication-title: Russ J Appl Chem
  doi: 10.1134/S107042720605017X
– volume: 2008
  start-page: 61
  year: 2008
  ident: 9439_CR67
  publication-title: Arkivoc
  doi: 10.3998/ark.5550190.0009.606
– volume: 8
  start-page: 356
  year: 2011
  ident: 9439_CR54
  publication-title: Curr Org Synth
  doi: 10.2174/157017911795529218
– volume: 26
  start-page: 2203
  year: 2008
  ident: 9439_CR7
  publication-title: Chin J Chem
  doi: 10.1002/cjoc.200890392
– volume: 65
  start-page: 6270
  year: 2000
  ident: 9439_CR39
  publication-title: J Org Chem
  doi: 10.1021/jo000711f
– volume: 127
  start-page: 16386
  year: 2005
  ident: 9439_CR63
  publication-title: J Am Chem Soc
  doi: 10.1021/ja056092f
– volume: 12
  start-page: 72
  year: 1978
  ident: 9439_CR17
  publication-title: Khim Farm Zh
– volume: 18
  start-page: 693
  year: 2007
  ident: 9439_CR56
  publication-title: Tetrahedron Asymmetry
  doi: 10.1016/j.tetasy.2007.03.002
– volume: 7
  start-page: 4141
  year: 2005
  ident: 9439_CR84
  publication-title: Org Lett
  doi: 10.1021/ol051476w
– ident: 9439_CR89
  doi: 10.1002/anie.200500297
– volume: 279
  start-page: 51131
  year: 2004
  ident: 9439_CR45
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M404857200
– volume: 47
  start-page: 631
  year: 1978
  ident: 9439_CR78
  publication-title: Russ Chem Rev
  doi: 10.1070/RC1978v047n07ABEH002243
– volume: 73
  start-page: 7651
  year: 2008
  ident: 9439_CR95
  publication-title: J Org Chem
  doi: 10.1021/jo801463j
– volume: 9
  start-page: 1573
  year: 1999
  ident: 9439_CR52
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(99)00227-9
– volume: 71
  start-page: 4663
  year: 2006
  ident: 9439_CR83
  publication-title: J Org Chem
  doi: 10.1021/jo060339p
– volume: 2010
  start-page: 3802
  year: 2010
  ident: 9439_CR60
  publication-title: Eur J Org Chem
  doi: 10.1002/ejoc.201000448
– volume: 23
  start-page: 1587
  year: 1958
  ident: 9439_CR81
  publication-title: J Org Chem
  doi: 10.1021/jo01104a629
– volume: 286
  start-page: 971
  year: 1999
  ident: 9439_CR30
  publication-title: Science
  doi: 10.1126/science.286.5441.971
– volume-title: Frontier orbitals and organic chemical reactions
  year: 1977
  ident: 9439_CR80
– volume: 41
  start-page: 826
  year: 2011
  ident: 9439_CR12
  publication-title: Synth Commun
  doi: 10.1080/00397911003668596
– volume: 32
  start-page: 656
  year: 2011
  ident: 9439_CR14
  publication-title: Bull Korean Chem Soc
  doi: 10.5012/bkcs.2011.32.2.656
– volume: 10
  start-page: 1917
  year: 2000
  ident: 9439_CR29
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(00)00374-7
– volume: 1
  start-page: 66
  year: 2012
  ident: 9439_CR53
  publication-title: Arkivoc
– volume: 68
  start-page: 7867
  year: 2012
  ident: 9439_CR64
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2012.07.027
– ident: 9439_CR74
  doi: 10.1021/ja065267y
– volume: 53
  start-page: 90
  year: 2009
  ident: 9439_CR4
  publication-title: J Korean Chem Soc
  doi: 10.5012/jkcs.2009.53.1.090
– volume: 1
  start-page: 67
  year: 2003
  ident: 9439_CR37
  publication-title: Synlett
– volume: 33
  start-page: 2629
  year: 1990
  ident: 9439_CR20
  publication-title: J Med Chem
  doi: 10.1021/jm00171a044
– volume: 42
  start-page: 2204
  year: 1999
  ident: 9439_CR23
  publication-title: J Med Chem
  doi: 10.1021/jm981114c
– volume: 9
  start-page: 989
  year: 2002
  ident: 9439_CR40
  publication-title: Chem Biol
  doi: 10.1016/S1074-5521(02)00212-0
– volume: 41
  start-page: 3969
  year: 2012
  ident: 9439_CR55
  publication-title: Chem Soc Rev
  doi: 10.1039/c2cs15361k
– volume: 127
  start-page: 16386
  year: 2005
  ident: 9439_CR61
  publication-title: J Am Chem Soc
  doi: 10.1021/ja056092f
– volume: 5
  start-page: 1
  year: 1973
  ident: 9439_CR79
  publication-title: Int J Chem Kinet
  doi: 10.1002/kin.550050102
– volume: 1
  start-page: 291
  year: 1991
  ident: 9439_CR21
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(01)80810-6
– volume: 2009
  start-page: 2356
  year: 2009
  ident: 9439_CR76
  publication-title: Synlett
  doi: 10.1055/s-0029-1217710
– volume: 17
  start-page: 2622
  year: 2007
  ident: 9439_CR85
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmcl.2007.01.111
– volume-title: Multicomponent reactions
  year: 2005
  ident: 9439_CR16
– volume: 43
  start-page: 2703
  year: 2000
  ident: 9439_CR42
  publication-title: J Med Chem
  doi: 10.1021/jm990612y
– volume: 29
  start-page: 57
  year: 2000
  ident: 9439_CR32
  publication-title: Chem Soc Rev
  doi: 10.1039/a903712h
– volume: 42
  start-page: 380
  year: 2007
  ident: 9439_CR50
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2006.09.003
– volume: 18
  start-page: 60
  year: 2008
  ident: 9439_CR43
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2007.11.027
– volume: 72
  start-page: 1417
  year: 2007
  ident: 9439_CR91
  publication-title: J Org Chem
  doi: 10.1021/jo0624187
– ident: 9439_CR72
– volume: 2009
  start-page: 3858
  year: 2009
  ident: 9439_CR66
  publication-title: Eur J Org Chem
  doi: 10.1002/ejoc.200900455
– volume: 10
  start-page: 175
  year: 2000
  ident: 9439_CR28
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/S0960-894X(99)00653-8
– volume: 2004
  start-page: 253
  year: 2004
  ident: 9439_CR34
  publication-title: Chem Commun
  doi: 10.1039/b309910e
– ident: 9439_CR25
  doi: 10.1021/jm990201h
– volume: 42
  start-page: 4794
  year: 1999
  ident: 9439_CR26
  publication-title: J Med Chem
  doi: 10.1021/jm990202+
– volume: 7
  start-page: 373
  year: 2006
  ident: 9439_CR6
  publication-title: Catal Commun
  doi: 10.1016/j.catcom.2005.12.007
– volume: 15
  start-page: 39
  year: 2011
  ident: 9439_CR75
  publication-title: Curr Org Chem
  doi: 10.2174/138527211793797837
– volume: 2
  start-page: 323
  year: 1994
  ident: 9439_CR22
  publication-title: Bioorg Med Chem
  doi: 10.1016/S0968-0896(00)82188-4
– volume: 131
  start-page: 15301
  year: 2009
  ident: 9439_CR62
  publication-title: J Am Chem Soc
  doi: 10.1021/ja905320q
– volume: 236
  start-page: 216
  year: 2005
  ident: 9439_CR13
  publication-title: J Mol Catal A
  doi: 10.1016/j.molcata.2005.04.033
– volume: 351
  start-page: 3057
  year: 2009
  ident: 9439_CR68
  publication-title: Adv Synth Catal
  doi: 10.1002/adsc.200900597
– reference: 19793966 - J Neurosci. 2009 Sep 30;29(39):12079-88
– reference: 22546840 - Chem Soc Rev. 2012 May 21;41(10):3969-4009
– reference: 17070617 - Eur J Med Chem. 2007 Mar;42(3):380-5
– reference: 21394354 - Org Biomol Chem. 2011 Apr 21;9(8):3050-4
– reference: 16973602 - J Biol Chem. 2006 Nov 3;281(44):33182-91
– reference: 10377225 - J Med Chem. 1999 Jun 17;42(12):2204-11
– reference: 12323373 - Chem Biol. 2002 Sep;9(9):989-96
– reference: 15912549 - Angew Chem Int Ed Engl. 2005 Jun 27;44(26):4077-9
– reference: 19785440 - J Am Chem Soc. 2009 Oct 28;131(42):15301-10
– reference: 17331715 - Bioorg Med Chem Lett. 2007 May 1;17(9):2622-8
– reference: 7922143 - Bioorg Med Chem. 1994 May;2(5):323-9
– reference: 10987976 - J Org Chem. 2000 Sep 22;65(19):6270-2
– reference: 10579840 - J Med Chem. 1999 Nov 18;42(23):4764-77
– reference: 16010324 - Chem Commun (Camb). 2005 Jul 28;(28):3562-4
– reference: 16869664 - Org Lett. 2006 Aug 3;8(16):3577-80
– reference: 17105279 - J Am Chem Soc. 2006 Nov 22;128(46):14802-3
– reference: 10893308 - J Med Chem. 2000 Jul 13;43(14):2703-18
– reference: 10579843 - J Med Chem. 1999 Nov 18;42(23):4804-13
– reference: 17828720 - Chemistry. 2007;13(32):8920-6
– reference: 2552119 - J Med Chem. 1989 Oct;32(10):2399-406
– reference: 19082754 - Mol Divers. 2009 Feb;13(1):5-25
– reference: 2391701 - J Med Chem. 1990 Sep;33(9):2629-35
– reference: 10579841 - J Med Chem. 1999 Nov 18;42(23):4778-93
– reference: 21192642 - J Org Chem. 2011 Jan 21;76(2):396-402
– reference: 16146372 - Org Lett. 2005 Sep 15;7(19):4141-4
– reference: 17603540 - Nat Chem Biol. 2007 Aug;3(8):498-507
– reference: 16479280 - Chem Commun (Camb). 2006 Feb 28;(8):819-24
– reference: 12574631 - Science. 2003 Feb 7;299(5608):893-6
– reference: 12525161 - Biochemistry. 2003 Jan 21;42(2):338-49
– reference: 17288387 - J Org Chem. 2007 Feb 16;72(4):1417-24
– reference: 21188287 - European J Org Chem. 2010 Jul 1;2010(20):3802-3805
– reference: 12735752 - Org Lett. 2003 May 15;5(10):1685-8
– reference: 10386938 - Bioorg Med Chem Lett. 1999 Jun 7;9(11):1573-6
– reference: 18246559 - Chemistry. 2008;14(10):3177-81
– reference: 15448148 - J Biol Chem. 2004 Dec 3;279(49):51131-40
– reference: 10542155 - Science. 1999 Oct 29;286(5441):971-4
– reference: 16749802 - J Org Chem. 2006 Jun 9;71(12):4663-6
– reference: 16305212 - J Am Chem Soc. 2005 Nov 30;127(47):16386-7
– reference: 12703794 - Chem Commun (Camb). 2003 Mar 21;(6):728-9
– reference: 10987417 - Bioorg Med Chem Lett. 2000 Sep 4;10(17):1917-20
– reference: 18767801 - J Org Chem. 2008 Oct 3;73(19):7651-6
– reference: 14740029 - Chem Commun (Camb). 2004 Feb 7;(3):253-65
– reference: 10579842 - J Med Chem. 1999 Nov 18;42(23):4794-803
– reference: 11248403 - Eur J Med Chem. 2000 Dec;35(12 ):1043-52
– reference: 16555849 - J Org Chem. 2006 Mar 31;71(7):2888-91
– reference: 18060774 - Bioorg Med Chem Lett. 2008 Jan 1;18(1):60-5
– reference: 10673105 - Bioorg Med Chem Lett. 2000 Jan 17;10(2):175-8
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Snippet The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli...
(ProQuest: ... denotes formulae and/or non-USASCII text omitted; see image) The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea,...
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SubjectTerms Acetoacetates - chemistry
Aldehydes - chemistry
Biochemistry
Biomedical and Life Sciences
Catalysis
Life Sciences
Organic Chemistry
Pharmacy
Polymer Sciences
Pyrimidinones - chemical synthesis
Short Review
Stereoisomerism
Urea - chemistry
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Title Recent progress in asymmetric Biginelli reaction
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