Catalyst-free synthesis of quinazoline derivatives using low melting sugar–urea–salt mixture as a solvent

Low melting mixture of maltose-dimethylurea (DMU)-NH4Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method furnished the corresponding quinazolines in high yields vi...

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Published inGreen chemistry : an international journal and green chemistry resource : GC Vol. 14; no. 5; pp. 1502 - 1506
Main Authors Zhang, Zhan-Hui, Zhang, Xiao-Nan, Mo, Li-Ping, Li, Yong-Xiao, Ma, Fei-Ping
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 01.05.2012
Royal Society of Chemistry
Subjects
aldehydes
ammonium acetate
biodegradability
Carbohydrates with 4, 5, 6, ... C atoms, dissacharides and oligosaccharides
Carbohydrates. Nucleosides and nucleotides
Chemistry
Chemistry, Multidisciplinary
Exact sciences and technology
Green & Sustainable Science & Technology
green chemistry
Heterocyclic compounds
Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
ketones
melting
Organic chemistry
oxidation
Physical Sciences
Preparations and properties
Science & Technology
Science & Technology - Other Topics
solvents
MULTICOMPONENT REACTIONS
REACTION MEDIA
HETEROCYCLES
ORGANIC-REACTIONS
ANTIINFLAMMATORY EVALUATION
MAGNETICALLY SEPARABLE CATALYST
ONE-POT PROCEDURE
POLYETHYLENE-GLYCOL
EFFICIENT
WATER
One pot reaction
Melting
Multicomponent reaction
Nitrogen heterocycle
Quinazoline derivatives
Oside
Aerobe
Maltose
Aldehyde
Ketone
Ammonium chloride
Urea
Catalyst-free reaction
Ureas
Oxidation
Chemical synthesis
Solvent
Ammonium Chlorides
Online AccessGet full text

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Abstract Low melting mixture of maltose-dimethylurea (DMU)-NH4Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method furnished the corresponding quinazolines in high yields via one-pot three-component reaction of 2-aminoaryl ketones, aldehyde, and ammonium acetate under aerobic oxidation conditions.
AbstractList Low melting mixture of maltose–dimethylurea (DMU)–NH₄Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method furnished the corresponding quinazolines in high yields via one-pot three-component reaction of 2-aminoaryl ketones, aldehyde, and ammonium acetate under aerobic oxidation conditions.
Low melting mixture of maltose-dimethylurea (DMU)-NH4Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method furnished the corresponding quinazolines in high yields via one-pot three-component reaction of 2-aminoaryl ketones, aldehyde, and ammonium acetate under aerobic oxidation conditions.
Low melting mixture of maltose-dimethylurea (DMU)-NH sub(4)Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method furnished the corresponding quinazolines in high yields viaone-pot three-component reaction of 2-aminoaryl ketones, aldehyde, and ammonium acetate under aerobic oxidation conditions.
Author Zhang, Xiao-Nan
Ma, Fei-Ping
Mo, Li-Ping
Li, Yong-Xiao
Zhang, Zhan-Hui
Author_xml – sequence: 1
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  surname: Zhang
  fullname: Zhang, Zhan-Hui
– sequence: 2
  givenname: Xiao-Nan
  surname: Zhang
  fullname: Zhang, Xiao-Nan
– sequence: 3
  givenname: Li-Ping
  surname: Mo
  fullname: Mo, Li-Ping
– sequence: 4
  givenname: Yong-Xiao
  surname: Li
  fullname: Li, Yong-Xiao
– sequence: 5
  givenname: Fei-Ping
  surname: Ma
  fullname: Ma, Fei-Ping
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Cites_doi 10.1039/b820740b
10.1039/b413546f
10.1016/j.bmcl.2008.09.108
10.1016/j.bmc.2010.11.057
10.1039/C0CS00013B
10.1039/c1gc15158d
10.1016/j.tetlet.2009.11.133
10.1039/c0gc00024h
10.1016/j.tet.2005.01.118
10.1039/c0gc00169d
10.1039/b917548m
10.1039/b814011a
10.1039/c0gc00716a
10.1016/j.tet.2010.10.041
10.1039/b803630f
10.1016/j.ejmech.2009.11.005
10.1002/jhet.444
10.1039/B917923B
10.1016/S0040-4039(03)00229-6
10.1039/c001628d
10.1039/b809498p
10.1039/c1gc15056a
10.1002/adsc.201100561
10.1039/b807379a
10.1016/j.ejmech.2010.07.063
10.1039/B603660K
10.1039/c002454f
10.2174/092986711794940824
10.1002/aoc.1799
10.1039/b821746g
10.1021/cr100162c
10.1002/cmdc.201100085
10.1021/ol1016756
10.1039/B414515A
10.1016/j.ejmech.2010.07.067
10.1039/c0gc00797h
10.1016/j.bmc.2010.11.059
10.1016/j.tet.2010.04.082
10.1016/j.ejmech.2011.03.015
10.1039/C0GC00468E
10.1021/ol102350v
10.1021/jm00267a021
10.1016/j.tet.2011.07.002
10.1021/cr9001098
10.1016/j.tet.2011.10.070
10.1016/j.bmcl.2011.05.031
10.1016/j.tetlet.2008.12.022
10.1021/co1000713
10.1002/anie.201006515
10.1039/c0gc00936a
10.1021/jo900629g
10.1021/cc100047j
10.2174/138527209789630514
10.1039/c1gc00009h
10.1002/adsc.200900715
10.1002/asia.201000310
10.2174/138527209789630505
10.1016/j.molcata.2008.09.003
10.1039/b923631g
10.1002/ardp.201000065
10.1039/c0gc00838a
10.1039/c1gc15470b
10.1021/ol100954x
10.1039/c1cc12308d
10.1080/00397910903395250
10.1002/adsc.200600248
10.1002/prac.19823240519
10.1039/c004250a
10.1039/b816551c
10.1021/co100055x
10.1016/j.ejmech.2010.06.013
10.1002/anie.200504285
10.1039/c0gc00468e
10.1039/b414515a
10.1039/c0cs00013b
10.1055/s-0030-1259960
10.1055/s-0028-1083147
10.1039/b917923b
10.1039/b603660k
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Issue 5
Keywords MULTICOMPONENT REACTIONS
REACTION MEDIA
HETEROCYCLES
ORGANIC-REACTIONS
ANTIINFLAMMATORY EVALUATION
MAGNETICALLY SEPARABLE CATALYST
ONE-POT PROCEDURE
POLYETHYLENE-GLYCOL
EFFICIENT
WATER
One pot reaction
Melting
Multicomponent reaction
Nitrogen heterocycle
Quinazoline derivatives
Oside
Aerobe
Maltose
Aldehyde
Ketone
Ammonium chloride
Urea
Catalyst-free reaction
Ureas
Oxidation
Chemical synthesis
Solvent
Ammonium Chlorides
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PublicationYear 2012
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Royal Society of Chemistry
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References Kumaravel (c2gc35258c-(cit2b)/*[position()=1]) 2009; 13
Zhang (c2gc35258c-(cit5c)/*[position()=1]) 2011; 67
Jiang (c2gc35258c-(cit32e)/*[position()=1]) 2010; 66
Feng (c2gc35258c-(cit4c)/*[position()=1]) 2010; 12
Szczepankiewicz (c2gc35258c-(cit38)/*[position()=1]) 2003; 44
Mello (c2gc35258c-(cit4d)/*[position()=1]) 2009; 11
Russ (c2gc35258c-(cit13)/*[position()=1]) 2011; 13
Wang (c2gc35258c-(cit34e)/*[position()=1]) 2011; 13
Dabiri (c2gc35258c-(cit36)/*[position()=1]) 2010; 40
Zhang (c2gc35258c-(cit7)/*[position()=1]) 2009; 11
Reinhardt (c2gc35258c-(cit8)/*[position()=1]) 2008; 10
Alafeefy (c2gc35258c-(cit16b)/*[position()=1]) 2010; 45
Sarma (c2gc35258c-(cit35)/*[position()=1]) 2011; 13
Abbott (c2gc35258c-(cit3a)/*[position()=1]) 2011; 13
Cruz-Lopez (c2gc35258c-(cit21d)/*[position()=1]) 2011; 18
Ohta (c2gc35258c-(cit26)/*[position()=1]) 2010; 12
Maheswari (c2gc35258c-(cit28)/*[position()=1]) 2010; 352
Zhang (c2gc35258c-(cit34d)/*[position()=1]) 2010; 12
Ilgen (c2gc35258c-(cit12)/*[position()=1]) 2009; 11
Asfaw (c2gc35258c-(cit33a)/*[position()=1]) 2011; 13
Liu (c2gc35258c-(cit34a)/*[position()=1]) 2008; 296
Isambert (c2gc35258c-(cit32b)/*[position()=1]) 2011; 40
Imperato (c2gc35258c-(cit9)/*[position()=1]) 2006; 348
Liu (c2gc35258c-(cit34c)/*[position()=1]) 2009; 50
Portela-Cubillo (c2gc35258c-(cit31a)/*[position()=1]) 2008
Kempter (c2gc35258c-(cit37)/*[position()=1]) 1982; 324
Leitner (c2gc35258c-(cit4b)/*[position()=1]) 2008; 10
Zhang (c2gc35258c-(cit27a)/*[position()=1]) 2010; 12
Jiang (c2gc35258c-(cit32a)/*[position()=1]) 2010; 5
Butler (c2gc35258c-(cit2a)/*[position()=1]) 2010; 110
Jessop (c2gc35258c-(cit33c)/*[position()=1]) 2011; 13
Noolvi (c2gc35258c-(cit18a)/*[position()=1]) 2011; 46
Gore (c2gc35258c-(cit14)/*[position()=1]) 2011; 13
Avalos (c2gc35258c-(cit33b)/*[position()=1]) 2006; 45
Huang (c2gc35258c-(cit23)/*[position()=1]) 2008
Truong (c2gc35258c-(cit30a)/*[position()=1]) 2010; 51
Lu (c2gc35258c-(cit5b)/*[position()=1]) 2011; 25
Imperato (c2gc35258c-(cit10)/*[position()=1]) 2005
El-Azab (c2gc35258c-(cit18b)/*[position()=1]) 2010; 45
Tiwari (c2gc35258c-(cit15)/*[position()=1]) 2010; 22
Portela-Cubillo (c2gc35258c-(cit31b)/*[position()=1]) 2009; 74
Imperato (c2gc35258c-(cit1c)/*[position()=1]) 2006; 8
Wang (c2gc35258c-(cit3c)/*[position()=1]) 2011; 13
Ruijter (c2gc35258c-(cit32c)/*[position()=1]) 2011; 50
Aliaga (c2gc35258c-(cit32f)/*[position()=1]) 2010; 8
Kumar (c2gc35258c-(cit19)/*[position()=1]) 2011; 21
Balakumar (c2gc35258c-(cit16a)/*[position()=1]) 2010; 45
Qiu (c2gc35258c-(cit30b)/*[position()=1]) 2010; 12
Liu (c2gc35258c-(cit34b)/*[position()=1]) 2008
Tambade (c2gc35258c-(cit32d)/*[position()=1]) 2009; 13
Strauss (c2gc35258c-(cit1b)/*[position()=1]) 2010; 12
Gao (c2gc35258c-(cit3b)/*[position()=1]) 2011; 13
Peng (c2gc35258c-(cit29)/*[position()=1]) 2010; 47
Adschiri (c2gc35258c-(cit4a)/*[position()=1]) 2011; 13
Yang (c2gc35258c-(cit21b)/*[position()=1]) 2011; 19
Kumar (c2gc35258c-(cit25)/*[position()=1]) 2005; 61
Han (c2gc35258c-(cit27b)/*[position()=1]) 2011; 47
Gu (c2gc35258c-(cit6a)/*[position()=1]) 2010; 12
Kim (c2gc35258c-(cit21c)/*[position()=1]) 2008; 18
Barraja (c2gc35258c-(cit20)/*[position()=1]) 2011; 6
Saari (c2gc35258c-(cit22)/*[position()=1]) 2011; 19
Zhang (c2gc35258c-(cit27c)/*[position()=1]) 2010; 46
Chen (c2gc35258c-(cit5a)/*[position()=1]) 2005; 7
Deng (c2gc35258c-(cit34f)/*[position()=1]) 2011; 13
Ilgen (c2gc35258c-(cit11)/*[position()=1]) 2009; 11
Kabri (c2gc35258c-(cit17)/*[position()=1]) 2010; 45
Liu (c2gc35258c-(cit34g)/*[position()=1]) 2012; 354
Martins (c2gc35258c-(cit1a)/*[position()=1]) 2009; 109
Kohl (c2gc35258c-(cit39)/*[position()=1]) 1973; 16
Boyapati (c2gc35258c-(cit21a)/*[position()=1]) 2010; 343
Kus (c2gc35258c-(cit4e)/*[position()=1]) 2012; 68
García (c2gc35258c-(cit6c)/*[position()=1]) 2010; 12
Alonso (c2gc35258c-(cit24)/*[position()=1]) 2010; 66
Karnakar (c2gc35258c-(cit27d)/*[position()=1]) 2011
Francos (c2gc35258c-(cit6b)/*[position()=1]) 2010; 12
Liu, YH (WOS:000300448400024) 2012; 354
Chen, J (WOS:000226703800003) 2005; 7
Zhang, XN (WOS:000294593400033) 2011; 67
Tiwari, R (WOS:000279844900025) 2010; 22
Peng, YY (WOS:000282489200038) 2010; 47
Han, B (WOS:000292113700076) 2011; 47
Kumaravel, K (WOS:000271391400006) 2009; 13
Jiang, HF (WOS:000285432900013) 2010; 66
Kim, YH (WOS:000260789600058) 2008; 18
Sarma, R (WOS:000288126300035) 2011; 13
Garcia, JI (WOS:000275379600013) 2010; 12
Avalos, M (WOS:000238501500005) 2006; 45
Boyapati, S (WOS:000284039000003) 2010; 343
Ilgen, F (WOS:000272382200006) 2009; 11
Russ, C (WOS:000286056300021) 2011; 13
Gore, S (WOS:000289171900037) 2011; 13
Butler, RN (WOS:000283395800018) 2010; 110
Deng, J (WOS:000294437300045) 2011; 13
Martins, MAP (WOS:000269773600008) 2009; 109
Jiang, B (WOS:000284515100001) 2010; 5
Imperato, G (WOS:000227186300018) 2005
Imperato, G (WOS:000241636100032) 2006; 348
Kumar, A (WOS:000292186400051) 2011; 21
Kus, NS (WOS:000300028800001) 2012; 68
Zhang, W (WOS:000267727800001) 2009; 11
Wang, XS (WOS:000288183000016) 2011; 13
Zhang, JT (WOS:000279911000010) 2010; 46
Abbott, AP (WOS:000288126300001) 2011; 13
Liu, YH (WOS:000261538500006) 2008; 296
Wang, HJ (WOS:000288183000013) 2011; 13
Ohta, Y (WOS:000281180700061) 2010; 12
Truong, VL (WOS:000274885600050) 2010; 51
Maheswari, CU (WOS:000275235800013) 2010; 352
Yang, SH (WOS:000287590500027) 2011; 19
Gu, YL (WOS:000279566300001) 2010; 12
Strauss, CR (WOS:000281152800002) 2010; 12
Ilgen, F (WOS:000266767400020) 2009; 11
Kumar, V (WOS:000227930800009) 2005; 61
Cruz-Lopez, O (WOS:000288989500001) 2011; 18
Zhang, ZH (WOS:000281629900007) 2010; 12
Adschiri, T (WOS:000291351500002) 2011; 13
Qiu, D (WOS:000284555600030) 2010; 12
Noolvi, MN (WOS:000291118600041) 2011; 46
Feng, XJ (WOS:000282586000012) 2010; 12
Reinhardt, D (WOS:000260408700007) 2008; 10
Jessop, PG (WOS:000291351500003) 2011; 13
Francos, J (WOS:000281613900005) 2010; 12
Szczepankiewicz, W (WOS:000181242600004) 2003; 44
Alonso, R (WOS:000278947100008) 2010; 66
Portela-Cubillo, F (WOS:000268139700004) 2009; 74
Asfaw, N (WOS:000290227800001) 2011; 13
Gao, J (WOS:000290227800022) 2011; 13
Leitner, W (WOS:000257280200001) 2008; 10
Balakumar, C (WOS:000283911300025) 2010; 45
Liu, YH (WOS:000263383400018) 2009; 50
Ruijter, E (WOS:000292642600004) 2011; 50
Kabri, Y (WOS:000274773300025) 2010; 45
Imperato, G (WOS:000242220500006) 2006; 8
Liu, YH (WOS:000260777300018) 2008
El-Azab, AS (WOS:000281568600082) 2010; 45
Portela-Cubillo, F (WOS:000256924500029) 2008
Isambert, N (WOS:000287585000015) 2011; 40
Lu, J (WOS:000292710400009) 2011; 25
Dabiri, M (WOS:000282590200011) 2010; 40
Zhang, JT (WOS:000278616800042) 2010; 12
Mello, R (WOS:000267727800016) 2009; 11
Tambade, PJ (WOS:000271391400005) 2009; 13
Saari, R (WOS:000287590500024) 2011; 19
Barraja, P (WOS:000292212100011) 2011; 6
Karnakar, K (WOS:000290206600007) 2011
Alafeefy, AM (WOS:000283911300030) 2010; 45
KEMPTER, G (WOS:A1982PS98100018) 1982; 324
Huang, C (WOS:000261742300019) 2008
Aliaga, MJ (WOS:000272613300005) 2010; 8
KOHL, H (WOS:A1973Q529800023) 1973; 16
References_xml – volume: 11
  start-page: 911
  year: 2009
  ident: c2gc35258c-(cit7)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b820740b
– volume: 7
  start-page: 64
  year: 2005
  ident: c2gc35258c-(cit5a)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b413546f
– volume: 22
  start-page: 5981
  year: 2010
  ident: c2gc35258c-(cit15)/*[position()=1]
  publication-title: Asian J. Chem.
– volume: 18
  start-page: 6279
  year: 2008
  ident: c2gc35258c-(cit21c)/*[position()=1]
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2008.09.108
– volume: 19
  start-page: 968
  year: 2011
  ident: c2gc35258c-(cit21b)/*[position()=1]
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/j.bmc.2010.11.057
– volume: 40
  start-page: 1347
  year: 2011
  ident: c2gc35258c-(cit32b)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C0CS00013B
– volume: 13
  start-page: 1380
  year: 2011
  ident: c2gc35258c-(cit4a)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c1gc15158d
– start-page: 1089
  year: 2011
  ident: c2gc35258c-(cit27d)/*[position()=1]
  publication-title: Synlett
– volume: 51
  start-page: 758
  year: 2010
  ident: c2gc35258c-(cit30a)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2009.11.133
– volume: 12
  start-page: 1340
  year: 2010
  ident: c2gc35258c-(cit1b)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c0gc00024h
– volume: 61
  start-page: 3533
  year: 2005
  ident: c2gc35258c-(cit25)/*[position()=1]
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2005.01.118
– volume: 12
  start-page: 1552
  year: 2010
  ident: c2gc35258c-(cit6b)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c0gc00169d
– volume: 11
  start-page: 1948
  year: 2009
  ident: c2gc35258c-(cit12)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b917548m
– start-page: 6333
  year: 2008
  ident: c2gc35258c-(cit23)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/b814011a
– volume: 13
  start-page: 471
  year: 2011
  ident: c2gc35258c-(cit3a)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c0gc00716a
– volume: 66
  start-page: 9721
  year: 2010
  ident: c2gc35258c-(cit32e)/*[position()=1]
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2010.10.041
– start-page: 2935
  year: 2008
  ident: c2gc35258c-(cit31a)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/b803630f
– volume: 45
  start-page: 616
  year: 2010
  ident: c2gc35258c-(cit17)/*[position()=1]
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2009.11.005
– volume: 47
  start-page: 1240
  year: 2010
  ident: c2gc35258c-(cit29)/*[position()=1]
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.444
– volume: 8
  start-page: 43
  year: 2010
  ident: c2gc35258c-(cit32f)/*[position()=1]
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/B917923B
– volume: 44
  start-page: 2015
  year: 2003
  ident: c2gc35258c-(cit38)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(03)00229-6
– volume: 12
  start-page: 1127
  year: 2010
  ident: c2gc35258c-(cit6a)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c001628d
– volume: 10
  start-page: 730
  year: 2008
  ident: c2gc35258c-(cit4b)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b809498p
– volume: 13
  start-page: 1182
  year: 2011
  ident: c2gc35258c-(cit3b)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c1gc15056a
– volume: 354
  start-page: 441
  year: 2012
  ident: c2gc35258c-(cit34g)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201100561
– volume: 10
  start-page: 1170
  year: 2008
  ident: c2gc35258c-(cit8)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b807379a
– volume: 45
  start-page: 4904
  year: 2010
  ident: c2gc35258c-(cit16a)/*[position()=1]
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2010.07.063
– volume: 8
  start-page: 1051
  year: 2006
  ident: c2gc35258c-(cit1c)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/B603660K
– volume: 46
  start-page: 5244
  year: 2010
  ident: c2gc35258c-(cit27c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/c002454f
– volume: 18
  start-page: 943
  year: 2011
  ident: c2gc35258c-(cit21d)/*[position()=1]
  publication-title: Curr. Med. Chem.
  doi: 10.2174/092986711794940824
– volume: 25
  start-page: 537
  year: 2011
  ident: c2gc35258c-(cit5b)/*[position()=1]
  publication-title: Appl. Organomet. Chem.
  doi: 10.1002/aoc.1799
– volume: 11
  start-page: 994
  year: 2009
  ident: c2gc35258c-(cit4d)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b821746g
– volume: 110
  start-page: 6302
  year: 2010
  ident: c2gc35258c-(cit2a)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr100162c
– volume: 6
  start-page: 1238
  year: 2011
  ident: c2gc35258c-(cit20)/*[position()=1]
  publication-title: ChemMedChem
  doi: 10.1002/cmdc.201100085
– volume: 12
  start-page: 3963
  year: 2010
  ident: c2gc35258c-(cit26)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol1016756
– start-page: 1170
  year: 2005
  ident: c2gc35258c-(cit10)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/B414515A
– volume: 45
  start-page: 4947
  year: 2010
  ident: c2gc35258c-(cit16b)/*[position()=1]
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2010.07.067
– volume: 13
  start-page: 1391
  year: 2011
  ident: c2gc35258c-(cit33c)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c0gc00797h
– volume: 19
  start-page: 939
  year: 2011
  ident: c2gc35258c-(cit22)/*[position()=1]
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/j.bmc.2010.11.059
– volume: 66
  start-page: 4469
  year: 2010
  ident: c2gc35258c-(cit24)/*[position()=1]
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2010.04.082
– volume: 46
  start-page: 2327
  year: 2011
  ident: c2gc35258c-(cit18a)/*[position()=1]
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2011.03.015
– volume: 13
  start-page: 156
  year: 2011
  ident: c2gc35258c-(cit13)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C0GC00468E
– volume: 12
  start-page: 5474
  year: 2010
  ident: c2gc35258c-(cit30b)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol102350v
– volume: 16
  start-page: 1045
  year: 1973
  ident: c2gc35258c-(cit39)/*[position()=1]
  publication-title: J. Med. Chem.
  doi: 10.1021/jm00267a021
– volume: 67
  start-page: 7426
  year: 2011
  ident: c2gc35258c-(cit5c)/*[position()=1]
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2011.07.002
– volume: 109
  start-page: 4140
  year: 2009
  ident: c2gc35258c-(cit1a)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr9001098
– volume: 68
  start-page: 949
  year: 2012
  ident: c2gc35258c-(cit4e)/*[position()=1]
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2011.10.070
– volume: 21
  start-page: 4353
  year: 2011
  ident: c2gc35258c-(cit19)/*[position()=1]
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2011.05.031
– volume: 50
  start-page: 916
  year: 2009
  ident: c2gc35258c-(cit34c)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2008.12.022
– start-page: 3314
  year: 2008
  ident: c2gc35258c-(cit34b)/*[position()=1]
  publication-title: Synthesis
– volume: 13
  start-page: 196
  year: 2011
  ident: c2gc35258c-(cit3c)/*[position()=1]
  publication-title: ACS Comb. Sci.
  doi: 10.1021/co1000713
– volume: 50
  start-page: 6234
  year: 2011
  ident: c2gc35258c-(cit32c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201006515
– volume: 13
  start-page: 1059
  year: 2011
  ident: c2gc35258c-(cit33a)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c0gc00936a
– volume: 74
  start-page: 4934
  year: 2009
  ident: c2gc35258c-(cit31b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo900629g
– volume: 12
  start-page: 643
  year: 2010
  ident: c2gc35258c-(cit34d)/*[position()=1]
  publication-title: J. Comb. Chem.
  doi: 10.1021/cc100047j
– volume: 13
  start-page: 1820
  year: 2009
  ident: c2gc35258c-(cit2b)/*[position()=1]
  publication-title: Curr. Org. Chem.
  doi: 10.2174/138527209789630514
– volume: 13
  start-page: 1009
  year: 2011
  ident: c2gc35258c-(cit14)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c1gc00009h
– volume: 352
  start-page: 341
  year: 2010
  ident: c2gc35258c-(cit28)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.200900715
– volume: 5
  start-page: 2318
  year: 2010
  ident: c2gc35258c-(cit32a)/*[position()=1]
  publication-title: Chem.–Asian J.
  doi: 10.1002/asia.201000310
– volume: 13
  start-page: 1805
  year: 2009
  ident: c2gc35258c-(cit32d)/*[position()=1]
  publication-title: Curr. Org. Chem.
  doi: 10.2174/138527209789630505
– volume: 296
  start-page: 42
  year: 2008
  ident: c2gc35258c-(cit34a)/*[position()=1]
  publication-title: J. Mol. Catal. A: Chem.
  doi: 10.1016/j.molcata.2008.09.003
– volume: 12
  start-page: 426
  year: 2010
  ident: c2gc35258c-(cit6c)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b923631g
– volume: 343
  start-page: 570
  year: 2010
  ident: c2gc35258c-(cit21a)/*[position()=1]
  publication-title: Arch. Pharm.
  doi: 10.1002/ardp.201000065
– volume: 13
  start-page: 718
  year: 2011
  ident: c2gc35258c-(cit35)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c0gc00838a
– volume: 13
  start-page: 2576
  year: 2011
  ident: c2gc35258c-(cit34f)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c1gc15470b
– volume: 12
  start-page: 2841
  year: 2010
  ident: c2gc35258c-(cit27a)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol100954x
– volume: 47
  start-page: 7818
  year: 2011
  ident: c2gc35258c-(cit27b)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/c1cc12308d
– volume: 40
  start-page: 3214
  year: 2010
  ident: c2gc35258c-(cit36)/*[position()=1]
  publication-title: Synth. Commun.
  doi: 10.1080/00397910903395250
– volume: 348
  start-page: 2243
  year: 2006
  ident: c2gc35258c-(cit9)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.200600248
– volume: 324
  start-page: 841
  year: 1982
  ident: c2gc35258c-(cit37)/*[position()=1]
  publication-title: J. Prakt. Chem.
  doi: 10.1002/prac.19823240519
– volume: 12
  start-page: 1758
  year: 2010
  ident: c2gc35258c-(cit4c)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/c004250a
– volume: 11
  start-page: 848
  year: 2009
  ident: c2gc35258c-(cit11)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/b816551c
– volume: 13
  start-page: 181
  year: 2011
  ident: c2gc35258c-(cit34e)/*[position()=1]
  publication-title: ACS Comb. Sci.
  doi: 10.1021/co100055x
– volume: 45
  start-page: 4188
  year: 2010
  ident: c2gc35258c-(cit18b)/*[position()=1]
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2010.06.013
– volume: 45
  start-page: 3904
  year: 2006
  ident: c2gc35258c-(cit33b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200504285
– volume: 110
  start-page: 6302
  year: 2010
  ident: WOS:000283395800018
  article-title: Water: Nature's Reaction Enforcer-Comparative Effects for Organic Synthesis "In-Water" and "On-Water"
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr100162c
– volume: 13
  start-page: 1805
  year: 2009
  ident: WOS:000271391400005
  article-title: Multicomponent Reactions Catalyzed by Lanthanides
  publication-title: CURRENT ORGANIC CHEMISTRY
– volume: 12
  start-page: 5474
  year: 2010
  ident: WOS:000284555600030
  article-title: Gold(III)-Catalyzed Halogenation of Aromatic Boronates with N-Halosuccinimides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol102350v
– volume: 12
  start-page: 1758
  year: 2010
  ident: WOS:000282586000012
  article-title: Preparation and application of SBA-15-supported palladium catalyst for Suzuki reaction in supercritical carbon dioxide
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c004250a
– volume: 13
  start-page: 156
  year: 2011
  ident: WOS:000286056300021
  article-title: Efficient preparation of beta-D-glucosyl and beta-D-mannosyl ureas and other N-glucosides in carbohydrate melts
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00468e
– volume: 74
  start-page: 4934
  year: 2009
  ident: WOS:000268139700004
  article-title: Microwave-Promoted Syntheses of Quinazolines and Dihydroquinazolines from 2-Aminoarylalkanone O-Phenyl Oximes
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo900629g
– volume: 12
  start-page: 3963
  year: 2010
  ident: WOS:000281180700061
  article-title: Direct Synthesis of Quinazolines through Copper-Catalyzed Reaction of Aniline-Derived Benzamidines
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol1016756
– volume: 45
  start-page: 3904
  year: 2006
  ident: WOS:000238501500005
  article-title: Greener media in chemical synthesis and processing
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200504285
– volume: 5
  start-page: 2318
  year: 2010
  ident: WOS:000284515100001
  article-title: Muliticomponent Reactions for the Synthesis of Heterocycles
  publication-title: CHEMISTRY-AN ASIAN JOURNAL
  doi: 10.1002/asia.201000310
– volume: 45
  start-page: 4904
  year: 2010
  ident: WOS:000283911300025
  article-title: Synthesis, anti-inflammatory evaluation and docking studies of some new fluorinated fused quinazolines
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2010.07.063
– volume: 12
  start-page: 1552
  year: 2010
  ident: WOS:000281613900005
  article-title: Palladium-catalyzed cycloisomerization of (Z)-enynols into furans using green solvents: glycerol vs. water
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00169d
– volume: 50
  start-page: 6234
  year: 2011
  ident: WOS:000292642600004
  article-title: Multicomponent Reaction Design in the Quest for Molecular Complexity and Diversity
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201006515
– volume: 13
  start-page: 1009
  year: 2011
  ident: WOS:000289171900037
  article-title: Efficient synthesis of 3,4-dihydropyrimidin-2-ones in low melting tartaric acid-urea mixtures
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c1gc00009h
– volume: 22
  start-page: 5981
  year: 2010
  ident: WOS:000279844900025
  article-title: Evaluation of Antibacterial Activity of Novel Quinazoline Derivatives
  publication-title: ASIAN JOURNAL OF CHEMISTRY
– volume: 13
  start-page: 1820
  year: 2009
  ident: WOS:000271391400006
  article-title: Multi-Component Reactions in Water
  publication-title: CURRENT ORGANIC CHEMISTRY
– volume: 46
  start-page: 2327
  year: 2011
  ident: WOS:000291118600041
  article-title: Synthesis and in vitro antitumor activity of substituted quinazoline and quinoxaline derivatives: Search for anticancer agent
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2011.03.015
– volume: 343
  start-page: 570
  year: 2010
  ident: WOS:000284039000003
  article-title: Synthesis, Antimicrobial Evaluation, and Docking Studies of Novel 4-Substituted Quinazoline Derivatives as DNA-Gyrase Inhibitors
  publication-title: ARCHIV DER PHARMAZIE
  doi: 10.1002/ardp.201000065
– volume: 10
  start-page: 1170
  year: 2008
  ident: WOS:000260408700007
  article-title: Evaluating the greenness of alternative reaction media
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b807379a
– volume: 11
  start-page: 848
  year: 2009
  ident: WOS:000266767400020
  article-title: Organic reactions in low melting mixtures based on carbohydrates and L-carnitine-a comparison
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b816551c
– start-page: 1170
  year: 2005
  ident: WOS:000227186300018
  article-title: Low-melting sugar-urea-salt mixtures as solvents for Diels-Alder reactions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b414515a
– volume: 11
  start-page: 994
  year: 2009
  ident: WOS:000267727800016
  article-title: Baeyer-Villiger oxidation of ketones with a silica-supported peracid in supercritical carbon dioxide under flow conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b821746g
– start-page: 2935
  year: 2008
  ident: WOS:000256924500029
  article-title: 2-(aminoaryl)alkanone O-phenyl oximes: versatile reagents for syntheses of quinazolines
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b803630f
– volume: 6
  start-page: 1238
  year: 2011
  ident: WOS:000292212100011
  article-title: Pyrrolo[3,2-h]quinazolines as Photochemotherapeutic Agents
  publication-title: CHEMMEDCHEM
  doi: 10.1002/cmdc.201100085
– volume: 40
  start-page: 1347
  year: 2011
  ident: WOS:000287585000015
  article-title: Multicomponent reactions and ionic liquids: a perfect synergy for eco-compatible heterocyclic synthesis
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c0cs00013b
– volume: 109
  start-page: 4140
  year: 2009
  ident: WOS:000269773600008
  article-title: Solvent-Free Heterocyclic Synthesis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr9001098
– volume: 47
  start-page: 7818
  year: 2011
  ident: WOS:000292113700076
  article-title: Efficient aerobic oxidative synthesis of 2-aryl quinazolines via benzyl C-H bond amination catalyzed by 4-hydroxy-TEMPO
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c1cc12308d
– volume: 68
  start-page: 949
  year: 2012
  ident: WOS:000300028800001
  article-title: Organic reactions in subcritical and supercritical water
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2011.10.070
– volume: 13
  start-page: 1391
  year: 2011
  ident: WOS:000291351500003
  article-title: Searching for green solvents
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00797h
– volume: 50
  start-page: 916
  year: 2009
  ident: WOS:000263383400018
  article-title: An efficient Friedel-Crafts alkylation of nitrogen heterocycles catalyzed by antimony trichloride/montmorillonite K-10
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2008.12.022
– volume: 25
  start-page: 537
  year: 2011
  ident: WOS:000292710400009
  article-title: An improved procedure for the synthesis of arylboronates by palladium-catalyzed coupling reaction of aryl halides and bis(pinacolato)diboron in polyethylene glycol
  publication-title: APPLIED ORGANOMETALLIC CHEMISTRY
  doi: 10.1002/aoc.1799
– volume: 16
  start-page: 1045
  year: 1973
  ident: WOS:A1973Q529800023
  article-title: SYNTHESIS AND CENTRAL NERVOUS-SYSTEM DEPRESSANT ACTIVITY OF SOME 2-ARYL-6-CHLORO-4-PHENYLQUINAZOLINES
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
– volume: 40
  start-page: 3214
  year: 2010
  ident: WOS:000282590200011
  article-title: ECOFRIENDLY AND EFFICIENT ONE-POT PROCEDURE FOR THE SYNTHESIS OF QUINAZOLINE DERIVATIVES CATALYZED BY AN ACIDIC IONIC LIQUID UNDER AEROBIC OXIDATION CONDITIONS
  publication-title: SYNTHETIC COMMUNICATIONS
  doi: 10.1080/00397910903395250
– volume: 352
  start-page: 341
  year: 2010
  ident: WOS:000275235800013
  article-title: Highly Efficient One-Pot Synthesis of 2-Substituted Quinazolines and 4H-Benzo[d][1,3]oxazines via Cross Dehydrogenative Coupling using Sodium Hypochlorite
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.200900715
– volume: 13
  start-page: 718
  year: 2011
  ident: WOS:000288126300035
  article-title: Microwave-promoted efficient synthesis of dihydroquinazolines
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00838a
– volume: 18
  start-page: 6279
  year: 2008
  ident: WOS:000260789600058
  article-title: Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2008.09.108
– volume: 296
  start-page: 42
  year: 2008
  ident: WOS:000261538500006
  article-title: Amberlyst-15 as a new and reusable catalyst for regioselective ring-opening reactions of epoxides to beta-alkoxy alcohols
  publication-title: JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
  doi: 10.1016/j.molcata.2008.09.003
– volume: 66
  start-page: 9721
  year: 2010
  ident: WOS:000285432900013
  article-title: L-Proline-catalyzed five-component domino reaction leading to multifunctionalized 1,2,3,4-tetrahydropyridines
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2010.10.041
– volume: 21
  start-page: 4353
  year: 2011
  ident: WOS:000292186400051
  article-title: Exploration of antimicrobial and antioxidant potential of newly synthesized 2,3-disubstituted quinazoline-4(3H)-ones
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2011.05.031
– volume: 13
  start-page: 181
  year: 2011
  ident: WOS:000288183000013
  article-title: Cerium Ammonium Nitrate-Catalyzed Multicomponent Reaction for Efficient Synthesis of Functionalized Tetrahydropyridines
  publication-title: ACS COMBINATORIAL SCIENCE
  doi: 10.1021/co100055x
– start-page: 6333
  year: 2008
  ident: WOS:000261742300019
  article-title: Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b814011a
– start-page: 1089
  year: 2011
  ident: WOS:000290206600007
  article-title: An Efficient Protocol for the Synthesis of 2-Phenylquinazolines Catalyzed by Ceric Ammonium Nitrate (CAN)
  publication-title: SYNLETT
  doi: 10.1055/s-0030-1259960
– volume: 11
  start-page: 911
  year: 2009
  ident: WOS:000267727800001
  article-title: Green chemistry aspects of fluorous techniques-opportunities and challenges for small-scale organic synthesis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b820740b
– volume: 45
  start-page: 4188
  year: 2010
  ident: WOS:000281568600082
  article-title: Design, synthesis and biological evaluation of novel quinazoline derivatives as potential antitumor agents: Molecular docking study
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2010.06.013
– volume: 67
  start-page: 7426
  year: 2011
  ident: WOS:000294593400033
  article-title: Nickel chloride-catalyzed one-pot three-component synthesis of pyrazolophthalazinyl spirooxindoles
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2011.07.002
– volume: 348
  start-page: 2243
  year: 2006
  ident: WOS:000241636100032
  article-title: Stille reactions with tetraalkylstannanes and phenyltrialkylstannanes in low melting sugar-urea-salt mixtures
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.200600248
– volume: 12
  start-page: 643
  year: 2010
  ident: WOS:000281629900007
  article-title: Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones by Three-Component Coupling of Isatoic Anhydride, Amines, and Aldehydes Catalyzed by Magnetic Fe3O4 Nanoparticles in Water
  publication-title: JOURNAL OF COMBINATORIAL CHEMISTRY
  doi: 10.1021/cc100047j
– start-page: 3314
  year: 2008
  ident: WOS:000260777300018
  article-title: Efficient Conversion of Epoxides into beta-Hydroperoxy Alcohols Catalyzed by Antimony Trichloride/SiO2
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0028-1083147
– volume: 45
  start-page: 616
  year: 2010
  ident: WOS:000274773300025
  article-title: Original quinazoline derivatives displaying antiplasmodial properties
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2009.11.005
– volume: 11
  start-page: 1948
  year: 2009
  ident: WOS:000272382200006
  article-title: Conversion of carbohydrates into 5-hydroxymethylfurfural in highly concentrated low melting mixtures
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b917548m
– volume: 18
  start-page: 943
  year: 2011
  ident: WOS:000288989500001
  article-title: Novel Substituted Quinazolines for Potent EGFR Tyrosine Kinase Inhibitors
  publication-title: CURRENT MEDICINAL CHEMISTRY
– volume: 12
  start-page: 1340
  year: 2010
  ident: WOS:000281152800002
  article-title: Accounting for clean, fast and high yielding reactions under microwave conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00024h
– volume: 45
  start-page: 4947
  year: 2010
  ident: WOS:000283911300030
  article-title: Synthesis, analgesic and anti-inflammatory evaluation of some novel quinazoline derivatives
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2010.07.067
– volume: 7
  start-page: 64
  year: 2005
  ident: WOS:000226703800003
  article-title: Polyethylene glycol and solutions of polyethylene glycol as green reaction media
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b413546f
– volume: 19
  start-page: 968
  year: 2011
  ident: WOS:000287590500027
  article-title: Virtual screening and synthesis of quinazolines as novel JAK2 inhibitors
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2010.11.057
– volume: 13
  start-page: 471
  year: 2011
  ident: WOS:000288126300001
  article-title: Processing of metals and metal oxides using ionic liquids
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00716a
– volume: 51
  start-page: 758
  year: 2010
  ident: WOS:000274885600050
  article-title: Mild and efficient ligand-free copper-catalyzed condensation for the synthesis of quinazolines
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2009.11.133
– volume: 19
  start-page: 939
  year: 2011
  ident: WOS:000287590500024
  article-title: Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2010.11.059
– volume: 66
  start-page: 4469
  year: 2010
  ident: WOS:000278947100008
  article-title: An efficient synthesis of quinazolines: a theoretical and experimental study on the photochemistry of oxime derivatives
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2010.04.082
– volume: 12
  start-page: 426
  year: 2010
  ident: WOS:000275379600013
  article-title: Green solvents from glycerol. Synthesis and physico-chemical properties of alkyl glycerol ethers
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b923631g
– volume: 12
  start-page: 2841
  year: 2010
  ident: WOS:000278616800042
  article-title: A Simple and Efficient Approach to the Synthesis of 2-Phenylquinazolines via sp(3) C-H Functionalization
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol100954x
– volume: 13
  start-page: 2576
  year: 2011
  ident: WOS:000294437300045
  article-title: Sulfonic acid supported on hydroxyapatite-encapsulated-gamma-Fe2O3 nanocrystallites as a magnetically separable catalyst for one-pot reductive amination of carbonyl compounds
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c1gc15470b
– volume: 12
  start-page: 1127
  year: 2010
  ident: WOS:000279566300001
  article-title: Glycerol as a sustainable solvent for green chemistry
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c001628d
– volume: 354
  start-page: 441
  year: 2012
  ident: WOS:000300448400024
  article-title: Triflic Acid-Functionalized Silica-Coated Magnetic Nanoparticles as a Magnetically Separable Catalyst for Synthesis of gem-Dihydroperoxides
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201100561
– volume: 13
  start-page: 1059
  year: 2011
  ident: WOS:000290227800001
  article-title: The 13 Principles of Green Chemistry and Engineering for a Greener Africa
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c0gc00936a
– volume: 10
  start-page: 730
  year: 2008
  ident: WOS:000257280200001
  article-title: Supercritical fluids in green chemistry
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b809498p
– volume: 46
  start-page: 5244
  year: 2010
  ident: WOS:000279911000010
  article-title: A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c002454f
– volume: 324
  start-page: 841
  year: 1982
  ident: WOS:A1982PS98100018
  article-title: HETEROCYCLES FROM ORTHO-AMINOKETONES .34. N-ALKYLATION AND DEHYDROGENATION OF 1,2,3,4-TETRAHYDROQUINAZOLINES
  publication-title: JOURNAL FUR PRAKTISCHE CHEMIE
– volume: 13
  start-page: 1380
  year: 2011
  ident: WOS:000291351500002
  article-title: Green materials synthesis with supercritical water
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c1gc15158d
– volume: 47
  start-page: 1240
  year: 2010
  ident: WOS:000282489200038
  article-title: A Convenient One-Pot Procedure for the Synthesis of 2-Aryl Quinazolines Using Active MnO2 as Oxidant
  publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY
  doi: 10.1002/jhet.444
– volume: 8
  start-page: 43
  year: 2010
  ident: WOS:000272613300005
  article-title: Impregnated copper on magnetite: an efficient and green catalyst for the multicomponent preparation of propargylamines under solvent free conditions
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/b917923b
– volume: 44
  start-page: 2015
  year: 2003
  ident: WOS:000181242600004
  article-title: Transformation of 5,5-diaryl-4,5-dihydro-1,2,4-oxadiazoles to 4-arylquinazolines
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/S0040-4039(03)00229-6
– volume: 61
  start-page: 3533
  year: 2005
  ident: WOS:000227930800009
  article-title: A catalyst- and solvent-free selective approach to biologically important quinazolines and benzo[g]quinazoline
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2005.01.118
– volume: 13
  start-page: 1182
  year: 2011
  ident: WOS:000290227800022
  article-title: Iron(III)-based ionic liquid-catalyzed regioselective benzylation of arenes and heteroarenes
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c1gc15056a
– volume: 13
  start-page: 196
  year: 2011
  ident: WOS:000288183000016
  article-title: Combinatorial Synthesis of 3-Arylideneaminoquinazolin-4(1H)-one Derivatives Catalyzed by Iodine in Ionic Liquids
  publication-title: ACS COMBINATORIAL SCIENCE
  doi: 10.1021/co1000713
– volume: 8
  start-page: 1051
  year: 2006
  ident: WOS:000242220500006
  article-title: Low melting sugar-urea-salt mixtures as solvents for organic reactions - estimation of polarity and use in catalysis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b603660k
SSID ssj0011764
Score 2.4636002
Snippet Low melting mixture of maltose-dimethylurea (DMU)-NH4Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the...
Low melting mixture of maltose-dimethylurea (DMU)-NH sub(4)Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in...
Low melting mixture of maltose–dimethylurea (DMU)–NH₄Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the...
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StartPage 1502
SubjectTerms aldehydes
ammonium acetate
biodegradability
Carbohydrates with 4, 5, 6, ... C atoms, dissacharides and oligosaccharides
Carbohydrates. Nucleosides and nucleotides
Chemistry
Chemistry, Multidisciplinary
Exact sciences and technology
Green & Sustainable Science & Technology
green chemistry
Heterocyclic compounds
Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
ketones
melting
Organic chemistry
oxidation
Physical Sciences
Preparations and properties
Science & Technology
Science & Technology - Other Topics
solvents
Title Catalyst-free synthesis of quinazoline derivatives using low melting sugar–urea–salt mixture as a solvent
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