Synthetic Strategies for Hydrazinyl Thiazole Derivatives

Hydrazinyl thiazole is frequently encountered in natural as well as in synthetic compounds. It is also an important pharmacophore and has some other useful applications. In this review article, we have compiled different green synthetic procedures for the synthesis of hydrazinyl thiazole derivatives...

Full description

Saved in:
Bibliographic Details
Published inChemistrySelect (Weinheim) Vol. 5; no. 48; pp. 15153 - 15166
Main Authors Dey, Sovan, Das, Arindam, Hossain, Md. Firoj
Format Journal Article
LanguageEnglish
Published 30.12.2020
Subjects
Green Chemistry
Hydrazinyl Thiazole
Multicomponent Reactions
Phenacyl bromide
Thiosemicarbazide
Online AccessGet full text

Cover

Abstract Hydrazinyl thiazole is frequently encountered in natural as well as in synthetic compounds. It is also an important pharmacophore and has some other useful applications. In this review article, we have compiled different green synthetic procedures for the synthesis of hydrazinyl thiazole derivatives. Also, the critical analysis of different synthetic schemes will help to understand the lacks in developed procedures and to develop new methodologies regarding its synthesis, specially using heterogeneous organocatalyst and photocatalyst. Hydrazinyl Thiazole, an important pharmacophore has been synthesized using different methodologies by different research groups. Here we have compiled different methodologies and also pointed out the advantages and disadvantages of reported protocols along with future scopes for further development in synthetic procedure.
AbstractList Hydrazinyl thiazole is frequently encountered in natural as well as in synthetic compounds. It is also an important pharmacophore and has some other useful applications. In this review article, we have compiled different green synthetic procedures for the synthesis of hydrazinyl thiazole derivatives. Also, the critical analysis of different synthetic schemes will help to understand the lacks in developed procedures and to develop new methodologies regarding its synthesis, specially using heterogeneous organocatalyst and photocatalyst. Hydrazinyl Thiazole, an important pharmacophore has been synthesized using different methodologies by different research groups. Here we have compiled different methodologies and also pointed out the advantages and disadvantages of reported protocols along with future scopes for further development in synthetic procedure.
Abstract Hydrazinyl thiazole is frequently encountered in natural as well as in synthetic compounds. It is also an important pharmacophore and has some other useful applications. In this review article, we have compiled different green synthetic procedures for the synthesis of hydrazinyl thiazole derivatives. Also, the critical analysis of different synthetic schemes will help to understand the lacks in developed procedures and to develop new methodologies regarding its synthesis, specially using heterogeneous organocatalyst and photocatalyst.
Author Dey, Sovan
Hossain, Md. Firoj
Das, Arindam
Author_xml – sequence: 1
  givenname: Sovan
  surname: Dey
  fullname: Dey, Sovan
  organization: University of North Bengal
– sequence: 2
  givenname: Arindam
  surname: Das
  fullname: Das, Arindam
  organization: University of North Bengal
– sequence: 3
  givenname: Md. Firoj
  orcidid: 0000-0003-1199-7881
  surname: Hossain
  fullname: Hossain, Md. Firoj
  email: firoj01982@nbu.ac.in
  organization: University of North Bengal
BookMark eNqFjz1PwzAURS1UJErpypw_kPBsx449ovBRpEgMCXNkOc_UKCTIjorSX0-rImBjune450rnkiyGcUBCrilkFIDdxN5OGQMGwLXmZ2TJuBSpFLle_OkXZB3jGwBQqSQTxZKoeh6mLU7eJvUUzISvHmPixpBs5i6YvR_mPmm23uzHHpM7DH5nJr_DeEXOnekjrr9zRV4e7ptyk1bPj0_lbZVapjRPWa6sENBJCco4WVAOFNA5a5GBo3mhBHAmuNC5y4VjvNOdOSCaGegcQ74i2enXhjHGgK79CP7dhLml0B7V26N6-6N-APQJ-PQ9zv-s27oqm1_2C9LxXxE
CitedBy_id crossref_primary_10_1016_j_ijbiomac_2022_09_102
crossref_primary_10_1039_D2OB02308C
crossref_primary_10_1002_slct_202102642
crossref_primary_10_2174_1570179419666220216122637
Cites_doi 10.1016/j.ejmech.2009.11.008
10.1016/S0960-894X(01)80574-6
10.1007/s11030-013-9474-6
10.1039/C4OB00360H
10.1016/j.jscs.2014.05.001
10.1016/j.ejmech.2005.01.013
10.1016/j.ejps.2013.11.001
10.1002/cber.188702002200
10.1002/slct.201802511
10.1016/j.ejmech.2006.12.025
10.1002/ardp.202000003
10.1016/j.ejmech.2012.11.046
10.1002/cbf.1266
10.1080/10426509608046376
10.1016/j.ejmech.2017.06.041
10.1016/j.ejmech.2010.03.039
10.1007/s12039-012-0285-6
10.1016/j.ejmech.2015.05.043
10.1039/B916237B
10.1007/s11030-018-9835-2
10.1002/slct.201904609
10.1016/j.ejmech.2008.10.031
10.1016/j.ejmech.2013.08.054
10.1016/j.ejmech.2010.10.027
10.1016/j.bmcl.2015.01.040
10.1080/17415993.2017.1371175
10.1016/j.tet.2011.09.105
10.3998/ark.5550190.0005.717
10.1002/jhet.3371
10.1016/j.ejmech.2007.07.001
10.1016/j.bmcl.2015.01.055
10.1515/hc-2016-0024
10.1016/j.ejmech.2010.11.032
10.1039/D0OB00109K
10.1007/s11030-015-9654-7
10.1038/s41598-017-17261-w
10.3390/ijms151222059
10.1016/j.tet.2013.08.034
10.1002/adsc.201701063
10.13005/ojc/340360
10.1007/s11172-009-0328-4
10.1071/CH06377
10.1021/jm00362a014
10.1016/j.ejmech.2006.12.001
10.1016/j.ultsonch.2011.10.017
10.1080/10426507.2010.492366
10.1016/j.ejmech.2010.07.048
10.1016/j.snb.2016.03.062
10.1135/cccc19862214
10.1016/j.bmcl.2011.06.076
10.1016/j.cclet.2012.10.002
10.1016/j.dyepig.2016.08.044
ContentType Journal Article
Copyright 2020 Wiley‐VCH GmbH
Copyright_xml – notice: 2020 Wiley‐VCH GmbH
DBID AAYXX
CITATION
DOI 10.1002/slct.202003993
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 2365-6549
EndPage 15166
ExternalDocumentID 10_1002_slct_202003993
SLCT202003993
Genre reviewArticle
GrantInformation_xml – fundername: University of North Bengal
– fundername: University Grants Commission
  funderid: F.30-515/2020(BSR); 9718
GroupedDBID 0R~
1OC
33P
AAHHS
AANLZ
AAZKR
ABCUV
ABDBF
ACCFJ
ACCZN
ACGFS
ACPOU
ACXQS
ADBBV
ADKYN
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEQDE
AEUYR
AFBPY
AFFPM
AHBTC
AITYG
AIURR
AIWBW
AJBDE
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMYDB
BFHJK
BMXJE
DCZOG
EBS
HGLYW
LATKE
LEEKS
LITHE
LOXES
LUTES
LYRES
MEWTI
O9-
ROL
SUPJJ
WOHZO
WXSBR
ZZTAW
AAYXX
CITATION
ID FETCH-LOGICAL-c2893-248c550d6608af6713010effcce20f1478503253594f45f23d9da8c592a0df2e3
ISSN 2365-6549
IngestDate Fri Aug 23 03:31:25 EDT 2024
Sat Aug 24 01:04:31 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 48
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c2893-248c550d6608af6713010effcce20f1478503253594f45f23d9da8c592a0df2e3
ORCID 0000-0003-1199-7881
PageCount 14
ParticipantIDs crossref_primary_10_1002_slct_202003993
wiley_primary_10_1002_slct_202003993_SLCT202003993
PublicationCentury 2000
PublicationDate December 30, 2020
2020-12-30
PublicationDateYYYYMMDD 2020-12-30
PublicationDate_xml – month: 12
  year: 2020
  text: December 30, 2020
  day: 30
PublicationDecade 2020
PublicationTitle ChemistrySelect (Weinheim)
PublicationYear 2020
References 2009; 44
1887; 20
2017; 7
2013; 69
2018; 360
2012; 124
2013; 62
2015; 100
2004; 7
2012; 19
1986; 25B
2020; 18
2009; 58
2018; 39
2020; 5
2018; 3
2013; 17
2006; 24
2014; 15
2011; 21
2016; 231
2007; 60
2014; 52
2018; 34
2012; 68
1983; 26
2012; 23
2014; 12
2015; 19
1986; 51
2010; 39
1998
1997
2018; 22
2017; 136
2017; 138
2010; 45
2016; 6
2015; 25
2006; 41
2020
2016; 20
2011; 46
2008; 43
2007; 42
2018; 55
1996; 113
1997; 36B
1994; 4
2011; 186
2016; 22
e_1_2_7_5_1
e_1_2_7_3_1
e_1_2_7_9_1
e_1_2_7_7_1
Hublikar M. (e_1_2_7_49_1) 2020
e_1_2_7_19_1
e_1_2_7_17_1
e_1_2_7_15_1
e_1_2_7_1_1
e_1_2_7_41_2
e_1_2_7_13_1
e_1_2_7_43_1
e_1_2_7_11_1
e_1_2_7_45_1
e_1_2_7_47_1
e_1_2_7_26_1
e_1_2_7_28_1
Singh J. (e_1_2_7_59_1) 2016; 6
Vardhan V. A. (e_1_2_7_40_2) 1997; 36
e_1_2_7_50_1
e_1_2_7_31_1
e_1_2_7_23_1
e_1_2_7_33_1
e_1_2_7_54_1
e_1_2_7_21_1
e_1_2_7_35_1
e_1_2_7_56_1
Shahriza W. A. (e_1_2_7_34_1) 2012; 124
e_1_2_7_37_1
e_1_2_7_58_1
e_1_2_7_39_2
Rao V. R. (e_1_2_7_38_2) 1986; 25
e_1_2_7_6_1
e_1_2_7_4_1
e_1_2_7_8_1
e_1_2_7_18_1
e_1_2_7_16_1
e_1_2_7_2_1
e_1_2_7_14_1
e_1_2_7_42_1
e_1_2_7_12_1
e_1_2_7_44_1
e_1_2_7_10_1
e_1_2_7_46_1
e_1_2_7_48_1
e_1_2_7_27_1
Anastas P. (e_1_2_7_29_1) 1998
Wender P. A. (e_1_2_7_30_1) 1997
Salar U. (e_1_2_7_25_1) 2017; 7
e_1_2_7_51_1
e_1_2_7_53_1
e_1_2_7_24_1
e_1_2_7_32_1
e_1_2_7_55_1
e_1_2_7_22_1
e_1_2_7_57_1
e_1_2_7_20_1
e_1_2_7_36_1
Tryambake P. T. (e_1_2_7_52_1) 2018; 34
References_xml – volume: 45
  start-page: 3490
  year: 2010
  end-page: 3496
  publication-title: Eur. J. Med. Chem.
– volume: 17
  start-page: 773
  year: 2013
  end-page: 780
  publication-title: Mol. Diversity
– volume: 45
  start-page: 5460
  year: 2010
  end-page: 5464
  publication-title: Eur. J. Med. Chem.
– volume: 39
  start-page: 638
  year: 2010
  end-page: 655
  publication-title: Chem. Soc. Rev.
– volume: 7
  start-page: 208
  year: 2004
  end-page: 222
  publication-title: Arkivoc
– volume: 36B
  start-page: 1085
  year: 1997
  publication-title: Indian J. Chem.
– volume: 25
  start-page: 1254
  year: 2015
  end-page: 1258
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 5
  start-page: 2778
  year: 2020
  end-page: 2786
  publication-title: ChemistrySelect
– volume: 4
  start-page: 1601
  year: 1994
  end-page: 1606
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 7
  start-page: 1
  year: 2017
  end-page: 17
  publication-title: Sci. Rep.
– volume: 42
  start-page: 948
  year: 2007
  end-page: 954
  publication-title: Eur. J. Med. Chem.
– volume: 3
  start-page: 11634
  year: 2018
  end-page: 11642
  publication-title: ChemistrySelect
– volume: 186
  start-page: 220
  year: 2011
  end-page: 224
  publication-title: Phosphorus Sulfur Silicon Relat. Elem.
– volume: 6
  start-page: 49164
  year: 2016
  end-page: 49172
  publication-title: RSCAdv.
– volume: 21
  start-page: 5589
  year: 2011
  end-page: 5593
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 68
  start-page: 363
  year: 2012
  end-page: 369
  publication-title: Tetrahedron
– year: 1998
– volume: 18
  start-page: 4575
  year: 2020
  end-page: 4582
  publication-title: Org. Biomol. Chem.
– volume: 25B
  start-page: 413
  year: 1986
  end-page: 415
  publication-title: Indian J. Chem.
– volume: 15
  start-page: 22059
  year: 2014
  end-page: 22072
  publication-title: Int. J. Mol. Sci.
– volume: 69
  start-page: 564
  year: 2013
  end-page: 576
  publication-title: Eur. J. Med. Chem.
– volume: 26
  start-page: 1158
  year: 1983
  end-page: 1163
  publication-title: J. Med. Chem.
– volume: 20
  start-page: 3118
  year: 1887
  end-page: 3132
  publication-title: Ber. Dtsch. Chem. Ges.
– volume: 62
  start-page: 508
  year: 2013
  end-page: 514
  publication-title: Eur. J. Med. Chem.
– volume: 24
  start-page: 547
  year: 2006
  end-page: 554
  publication-title: Cell Biochem. Funct.
– volume: 22
  start-page: 243
  year: 2016
  end-page: 246
  publication-title: Heterocycl. Commun.
– volume: 41
  start-page: 201
  year: 2006
  end-page: 207
  publication-title: Eur. J. Med. Chem.
– volume: 60
  start-page: 302
  year: 2007
  end-page: 304
  publication-title: Aust. J. Chem.
– volume: 46
  start-page: 526
  year: 2011
  end-page: 534
  publication-title: Eur. J. Med. Chem.
– year: 2020
  publication-title: Archiv der Pharmazie.
– volume: 42
  start-page: 807
  year: 2007
  end-page: 816
  publication-title: Eur. J. Med. Chem.
– volume: 360
  start-page: 995
  year: 2018
  end-page: 1006
  publication-title: Adv. Synth. Catal.
– volume: 46
  start-page: 378
  year: 2011
  end-page: 382
  publication-title: Eur. J. Med. Chem.
– volume: 51
  start-page: 2214
  year: 1986
  end-page: 2221
  publication-title: Collect. Czech. Chem. Commun.
– volume: 58
  start-page: 2362
  year: 2009
  end-page: 2368
  publication-title: Russ. Chem. Bull.
– volume: 12
  start-page: 4663
  year: 2014
  end-page: 4672
  publication-title: Org. Biomol. Chem.
– volume: 136
  start-page: 140
  year: 2017
  end-page: 144
  publication-title: Dyes Pigm.
– volume: 34
  start-page: 1646
  year: 2018
  end-page: 1652
  publication-title: Orient. J. Chem.
– volume: 39
  start-page: 1
  year: 2018
  end-page: 7
  publication-title: J. Sulfur Chem.
– start-page: 765
  year: 1997
  publication-title: Chem Ind (London)
– volume: 19
  start-page: 475
  year: 2012
  end-page: 478
  publication-title: Ultrason. Sonochem.
– volume: 23
  start-page: 1221
  year: 2012
  end-page: 1224
  publication-title: Chin. Chem. Lett.
– volume: 100
  start-page: 1
  year: 2015
  end-page: 9
  publication-title: Eur. J. Med. Chem.
– volume: 20
  start-page: 497
  year: 2016
  end-page: 506
  publication-title: Mol. Diversity
– volume: 124
  start-page: 927
  year: 2012
  end-page: 931
  publication-title: J. Chem. Sci.
– volume: 231
  start-page: 847
  year: 2016
  end-page: 859
  publication-title: Sens. Actuators B
– volume: 55
  start-page: 2946
  year: 2018
  end-page: 2950
  publication-title: J. Heterocycl. Chem.
– volume: 52
  start-page: 138
  year: 2014
  end-page: 145
  publication-title: Eur. J. Pharm. Sci.
– volume: 113
  start-page: 47
  year: 1996
  end-page: 51
  publication-title: Phosphorus Sulfur Silicon Relat. Elem.
– volume: 138
  start-page: 255
  year: 2017
  end-page: 272
  publication-title: Eur. J. Med. Chem.
– volume: 44
  start-page: 2184
  year: 2009
  end-page: 2189
  publication-title: Eur. J. Med. Chem.
– volume: 25
  start-page: 1306
  year: 2015
  end-page: 1309
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 19
  start-page: 200
  year: 2015
  end-page: 206
  publication-title: J. Saudi Chem. Soc.
– volume: 69
  start-page: 9056
  year: 2013
  end-page: 9062
  publication-title: Tetrahedron
– volume: 43
  start-page: 981
  year: 2008
  end-page: 985
  publication-title: Eur. J. Med. Chem.
– volume: 22
  start-page: 841
  year: 2018
  end-page: 861
  publication-title: Mol. Diversity
– volume: 45
  start-page: 651
  year: 2010
  end-page: 660
  publication-title: Eur. J. Med. Chem.
– ident: e_1_2_7_7_1
  doi: 10.1016/j.ejmech.2009.11.008
– ident: e_1_2_7_3_1
  doi: 10.1016/S0960-894X(01)80574-6
– ident: e_1_2_7_4_1
  doi: 10.1007/s11030-013-9474-6
– ident: e_1_2_7_28_1
  doi: 10.1039/C4OB00360H
– ident: e_1_2_7_44_1
  doi: 10.1016/j.jscs.2014.05.001
– ident: e_1_2_7_10_1
  doi: 10.1016/j.ejmech.2005.01.013
– ident: e_1_2_7_20_1
  doi: 10.1016/j.ejps.2013.11.001
– ident: e_1_2_7_36_1
  doi: 10.1002/cber.188702002200
– ident: e_1_2_7_54_1
  doi: 10.1002/slct.201802511
– ident: e_1_2_7_12_1
  doi: 10.1016/j.ejmech.2006.12.025
– start-page: e2000003
  year: 2020
  ident: e_1_2_7_49_1
  publication-title: Archiv der Pharmazie.
  doi: 10.1002/ardp.202000003
  contributor:
    fullname: Hublikar M.
– ident: e_1_2_7_5_1
  doi: 10.1016/j.ejmech.2012.11.046
– ident: e_1_2_7_6_1
  doi: 10.1002/cbf.1266
– ident: e_1_2_7_41_2
  doi: 10.1080/10426509608046376
– ident: e_1_2_7_21_1
  doi: 10.1016/j.ejmech.2017.06.041
– ident: e_1_2_7_11_1
  doi: 10.1016/j.ejmech.2010.03.039
– volume: 124
  start-page: 927
  year: 2012
  ident: e_1_2_7_34_1
  publication-title: J. Chem. Sci.
  doi: 10.1007/s12039-012-0285-6
  contributor:
    fullname: Shahriza W. A.
– volume: 6
  start-page: 49164
  year: 2016
  ident: e_1_2_7_59_1
  publication-title: RSCAdv.
  contributor:
    fullname: Singh J.
– volume: 36
  start-page: 1085
  year: 1997
  ident: e_1_2_7_40_2
  publication-title: Indian J. Chem.
  contributor:
    fullname: Vardhan V. A.
– ident: e_1_2_7_15_1
  doi: 10.1016/j.ejmech.2015.05.043
– ident: e_1_2_7_27_1
  doi: 10.1039/B916237B
– ident: e_1_2_7_22_1
  doi: 10.1007/s11030-018-9835-2
– ident: e_1_2_7_48_1
  doi: 10.1002/slct.201904609
– ident: e_1_2_7_14_1
  doi: 10.1016/j.ejmech.2008.10.031
– ident: e_1_2_7_17_1
  doi: 10.1016/j.ejmech.2013.08.054
– ident: e_1_2_7_37_1
– volume-title: Oxford Science Publications
  year: 1998
  ident: e_1_2_7_29_1
  contributor:
    fullname: Anastas P.
– ident: e_1_2_7_9_1
  doi: 10.1016/j.ejmech.2010.10.027
– ident: e_1_2_7_24_1
  doi: 10.1016/j.bmcl.2015.01.040
– ident: e_1_2_7_47_1
  doi: 10.1080/17415993.2017.1371175
– ident: e_1_2_7_31_1
  doi: 10.1016/j.tet.2011.09.105
– ident: e_1_2_7_32_1
  doi: 10.3998/ark.5550190.0005.717
– ident: e_1_2_7_57_1
  doi: 10.1002/jhet.3371
– ident: e_1_2_7_16_1
  doi: 10.1016/j.ejmech.2007.07.001
– ident: e_1_2_7_23_1
  doi: 10.1016/j.bmcl.2015.01.055
– ident: e_1_2_7_51_1
  doi: 10.1515/hc-2016-0024
– ident: e_1_2_7_13_1
  doi: 10.1016/j.ejmech.2010.11.032
– ident: e_1_2_7_58_1
  doi: 10.1039/D0OB00109K
– ident: e_1_2_7_53_1
  doi: 10.1007/s11030-015-9654-7
– volume: 7
  start-page: 1
  year: 2017
  ident: e_1_2_7_25_1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-017-17261-w
  contributor:
    fullname: Salar U.
– ident: e_1_2_7_43_1
  doi: 10.3390/ijms151222059
– ident: e_1_2_7_35_1
  doi: 10.1016/j.tet.2013.08.034
– ident: e_1_2_7_1_1
– ident: e_1_2_7_55_1
  doi: 10.1002/adsc.201701063
– volume: 34
  start-page: 1646
  year: 2018
  ident: e_1_2_7_52_1
  publication-title: Orient. J. Chem.
  doi: 10.13005/ojc/340360
  contributor:
    fullname: Tryambake P. T.
– ident: e_1_2_7_33_1
  doi: 10.1007/s11172-009-0328-4
– start-page: 765
  year: 1997
  ident: e_1_2_7_30_1
  publication-title: Chem Ind (London)
  contributor:
    fullname: Wender P. A.
– ident: e_1_2_7_46_1
  doi: 10.1071/CH06377
– volume: 25
  start-page: 413
  year: 1986
  ident: e_1_2_7_38_2
  publication-title: Indian J. Chem.
  contributor:
    fullname: Rao V. R.
– ident: e_1_2_7_2_1
  doi: 10.1021/jm00362a014
– ident: e_1_2_7_19_1
  doi: 10.1016/j.ejmech.2006.12.001
– ident: e_1_2_7_42_1
  doi: 10.1016/j.ultsonch.2011.10.017
– ident: e_1_2_7_45_1
  doi: 10.1080/10426507.2010.492366
– ident: e_1_2_7_8_1
  doi: 10.1016/j.ejmech.2010.07.048
– ident: e_1_2_7_26_1
  doi: 10.1016/j.snb.2016.03.062
– ident: e_1_2_7_39_2
  doi: 10.1135/cccc19862214
– ident: e_1_2_7_18_1
  doi: 10.1016/j.bmcl.2011.06.076
– ident: e_1_2_7_50_1
  doi: 10.1016/j.cclet.2012.10.002
– ident: e_1_2_7_56_1
  doi: 10.1016/j.dyepig.2016.08.044
SSID ssj0001686257
Score 2.2081385
Snippet Hydrazinyl thiazole is frequently encountered in natural as well as in synthetic compounds. It is also an important pharmacophore and has some other useful...
Abstract Hydrazinyl thiazole is frequently encountered in natural as well as in synthetic compounds. It is also an important pharmacophore and has some other...
SourceID crossref
wiley
SourceType Aggregation Database
Publisher
StartPage 15153
SubjectTerms Green Chemistry
Hydrazinyl Thiazole
Multicomponent Reactions
Phenacyl bromide
Thiosemicarbazide
Title Synthetic Strategies for Hydrazinyl Thiazole Derivatives
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fslct.202003993
Volume 5
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3JTsMwELVYDnBBrKJsygGJA0pJvWQ5lpaqQsClRXCLnNgRIEhRKUjl6xnbiZMKxHaJWsduE8_LeMaZeYPQIfGDKJUt4foJwS6NEnjmvITCcxUKMKAFI1QlCl9e-f1ren7LbqtwW51dMkma6fuXeSX_kSq0gVxVluwfJGt_FBrgM8gXjiBhOP5KxoNpDvabolwtSWalplc47k_FWPFGT3VhTv6uQgi7cEVvmub7pW6RdsqKbwNdEUdZnDfyPr-Tqsyy3SXoFjFho7cKTV2TC9YeK7f-yeIDVl1uiAkuRfO4dz8ePdS3FrAO0yjekmgNhFUInM8Mp2hTftFWqFBWQ4ohziz0oTKXSG1xhe-myMonzW2YYF8eUxXgqiLmoohUa1T5Xt72ZN_31Qv04KIztOfn0SIGXQRKcLF92j3tVRtxKkdGM8LaWyvJPT18MvsnM8ZL3ZnR1shwFa0UboTTNphYQ3MyX0dLVpYbKLTYcCpsOIANp8KGU2LDqWFjE133zoadvltUyXBTcJaJi2mYgpspfN8LeeYHYJS0PJllaSqxl7VoEDKPYEZYRDPKMkxEJDgMiTD3RIYl2UIL-SiX28jBKRj8MEAkPKAioIn2hynnvqQRZ6yBjsrbj58NGUpsaK9xrCYqthPVQFjPzg_d4hkR7fxn0C5arqC7hxYm41e5D3biJDkoJP0BSLBenA
link.rule.ids 315,783,787,27936,27937
linkProvider EBSCOhost
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Synthetic+Strategies+for+Hydrazinyl+Thiazole+Derivatives&rft.jtitle=ChemistrySelect+%28Weinheim%29&rft.au=Dey%2C+Sovan&rft.au=Das%2C+Arindam&rft.au=Hossain%2C+Md.+Firoj&rft.date=2020-12-30&rft.issn=2365-6549&rft.eissn=2365-6549&rft.volume=5&rft.issue=48&rft.spage=15153&rft.epage=15166&rft_id=info:doi/10.1002%2Fslct.202003993&rft.externalDBID=10.1002%252Fslct.202003993&rft.externalDocID=SLCT202003993
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2365-6549&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2365-6549&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2365-6549&client=summon