A recent overview on the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles

Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The synthesis of this category of diverse fully functionalized 1,2,3-triazoles has become a necessary and unique research subject in modern syntheti...

Full description

Saved in:
Bibliographic Details
Published inBeilstein journal of organic chemistry Vol. 17; no. 1; pp. 1600 - 1628
Main Authors Shiri, Pezhman, Amani, Ali Mohammad, Mayer-Gall, Thomas
Format Journal Article
LanguageEnglish
Published Frankfurt am Main Beilstein-Institut zur Föerderung der Chemischen Wissenschaften 13.07.2021
Beilstein-Institut
Subjects
1,4,5-trisubstituted 1,2,3-triazoles
[3 + 2]‐cycloaddition
Azide
azides
Catalysis
Chemistry
click reaction
fully functionalized 1,2,3-triazoles
n-containing heterocycles
Review
Triazoles
Online AccessGet full text
ISSN1860-5397
2195-951X
1860-5397
DOI10.3762/bjoc.17.114

Cover

Abstract Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The synthesis of this category of diverse fully functionalized 1,2,3-triazoles has become a necessary and unique research subject in modern synthetic organic key transformations in academia, pharmacy, and industry. The current review aims to cover a wide literature survey of numerous synthetic strategies. Recent reports (2017–2021) in the field of 1,4,5-trisubstituted 1,2,3-triazoles are emphasized in this current review.
AbstractList Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The synthesis of this category of diverse fully functionalized 1,2,3-triazoles has become a necessary and unique research subject in modern synthetic organic key transformations in academia, pharmacy, and industry. The current review aims to cover a wide literature survey of numerous synthetic strategies. Recent reports (2017-2021) in the field of 1,4,5-trisubstituted 1,2,3-triazoles are emphasized in this current review.Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The synthesis of this category of diverse fully functionalized 1,2,3-triazoles has become a necessary and unique research subject in modern synthetic organic key transformations in academia, pharmacy, and industry. The current review aims to cover a wide literature survey of numerous synthetic strategies. Recent reports (2017-2021) in the field of 1,4,5-trisubstituted 1,2,3-triazoles are emphasized in this current review.
Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The synthesis of this category of diverse fully functionalized 1,2,3-triazoles has become a necessary and unique research subject in modern synthetic organic key transformations in academia, pharmacy, and industry. The current review aims to cover a wide literature survey of numerous synthetic strategies. Recent reports (2017–2021) in the field of 1,4,5-trisubstituted 1,2,3-triazoles are emphasized in this current review.
Author Amani, Ali Mohammad
Mayer-Gall, Thomas
Shiri, Pezhman
AuthorAffiliation 4 Deutsches Textilforschungszentrum Nord-West gGmbH, Adlerstr. 1, 47798 Krefeld, Germany
1 Department of Medical Nanotechnology, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
3 Department of Physical Chemistry and Center of Nanointegration (CENIDE), University of Duisburg-Essen, Universitätsstr. 2, 45141 Essen, Germany
2 Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
AuthorAffiliation_xml – name: 3 Department of Physical Chemistry and Center of Nanointegration (CENIDE), University of Duisburg-Essen, Universitätsstr. 2, 45141 Essen, Germany
– name: 1 Department of Medical Nanotechnology, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
– name: 4 Deutsches Textilforschungszentrum Nord-West gGmbH, Adlerstr. 1, 47798 Krefeld, Germany
– name: 2 Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
Author_xml – sequence: 1
  givenname: Pezhman
  orcidid: 0000-0003-0071-6570
  surname: Shiri
  fullname: Shiri, Pezhman
– sequence: 2
  givenname: Ali Mohammad
  orcidid: 0000-0002-7034-3071
  surname: Amani
  fullname: Amani, Ali Mohammad
– sequence: 3
  givenname: Thomas
  surname: Mayer-Gall
  fullname: Mayer-Gall, Thomas
BookMark eNptkV1rFTEQhoNU7Ide-QcWvBE855jJ5-6NUIoflYI3eh2yyWybw55NTbKn1F9v1lPEFq8mzDx5GOY9JUdTnJCQ10A3XCv2vt9GtwG9ARDPyAm0iq4l7_TRP-9jcprzllJBFVUvyDEXXAqt6Qn5et4kdDiVJu4x7QPeNXFqyg02-X6qJYfcxKGBlVjJdUkhz30uocwFfW2yFV-a9lccMb8kzwc7Znz1UM_Ij08fv198WV99-3x5cX61dkKysnaDG7SwjAMHQGtbZ6VoZd8r7uXglZa9Ym7oGHqUqu3UAFJJrXhFO-k9PyOXB6-PdmtuU9jZdG-iDeZPI6ZrY1MJbkQDtMd-aBEpZ0IgWuBSCfAgNAjvdHV9OLhu536HfjlEsuMj6ePJFG7MddyblnUUAKrg7YMgxZ8z5mJ2ITscRzthnLNhUnaCacZ5Rd88QbdxTlM9VaU6yVpKaVupdwfKpZhzwuHvMkDNkrdZ8jagTc270vCEdqHYEuKybRj_--c3JySt_g
CitedBy_id crossref_primary_10_1080_10406638_2022_2105904
crossref_primary_10_1002_ajoc_202200514
crossref_primary_10_3390_molecules27175559
crossref_primary_10_1007_s00726_024_03430_5
crossref_primary_10_1039_D4OB01671H
crossref_primary_10_1007_s11030_022_10510_9
crossref_primary_10_1039_D2OB00908K
crossref_primary_10_1039_D2OB00635A
crossref_primary_10_1002_ejoc_202200317
crossref_primary_10_1021_acsomega_3c06264
crossref_primary_10_2174_1385272826666220822124705
crossref_primary_10_2174_1570179420666230418123350
crossref_primary_10_1016_j_molstruc_2023_135181
crossref_primary_10_1002_ejoc_202300604
crossref_primary_10_1016_j_bmcl_2022_128800
crossref_primary_10_3762_bjoc_19_111
crossref_primary_10_1002_adsc_202200094
crossref_primary_10_1002_ejoc_202301135
crossref_primary_10_1007_s10593_023_03192_0
crossref_primary_10_1039_D3DT00651D
crossref_primary_10_1016_j_steroids_2022_109133
crossref_primary_10_1055_a_2060_3488
crossref_primary_10_32628_IJSRST52310563
crossref_primary_10_1007_s11030_022_10562_x
crossref_primary_10_1016_j_matchemphys_2021_125242
crossref_primary_10_1016_j_molstruc_2022_133412
crossref_primary_10_1002_tcr_202400107
crossref_primary_10_1016_j_molstruc_2023_134902
crossref_primary_10_1016_j_molstruc_2023_135179
crossref_primary_10_1515_znc_2022_0010
crossref_primary_10_2174_1570179420666221118100525
crossref_primary_10_3390_catal12101163
crossref_primary_10_1016_j_mencom_2021_09_006
Cites_doi 10.1021/acs.accounts.9b00549
10.1002/adsc.201601388
10.1016/j.jorganchem.2019.06.013
10.1002/ejoc.202000999
10.1021/cr900107r
10.1039/c9gc01129c
10.1007/s10562-017-2173-7
10.1021/jacs.9b09330
10.1021/acsomega.9b01285
10.1002/chem.202003386
10.2174/0929867327666200219141652
10.1002/adsc.201800394
10.1002/chem.201601703
10.1080/00304948.2011.593999
10.7324/japs.2020.1010016
10.1021/acs.joc.8b00573
10.1002/aoc.4974
10.1039/c7nj04271j
10.1002/slct.201801905
10.1021/acs.orglett.9b02269
10.1039/d0gc00569j
10.1016/j.ejmech.2014.12.012
10.1002/chem.201902901
10.1039/c9ob01175g
10.1016/j.nurt.2006.11.006
10.2174/1389557520666201027160436
10.1016/j.tet.2019.05.046
10.1007/s41061-015-0001-3
10.1002/ejoc.201901305
10.1016/j.ccr.2020.213217
10.1002/ejoc.201900889
10.1021/acs.orglett.0c00394
10.1039/c9sc06377c
10.1016/j.ejmech.2020.112712
10.1002/slct.201803418
10.1002/ajoc.201800340
10.1002/ejoc.201901249
10.1016/j.jcat.2019.07.063
10.1021/acs.joc.8b02916
10.1039/c9ob01156k
10.1039/d0ob00848f
10.3390/molecules24081533
10.1002/aoc.5319
10.1016/j.ejmech.2019.07.043
10.1128/aac.01436-16
10.1002/jhet.4174
10.1002/aoc.5600
10.1007/s10593-018-2343-6
10.1016/j.bmcl.2017.11.038
10.1002/slct.201902362
10.1016/j.bioorg.2019.103162
10.1007/s10719-019-09883-1
10.1002/ardp.202000163
10.1021/acs.orglett.8b01002
10.1039/c8ob00533h
10.1002/cjoc.201900556
10.1021/acs.joc.0c00520
10.1021/acs.joc.9b01817
10.1016/j.jddst.2019.101130
10.1016/j.tet.2017.10.003
10.1055/s-0034-1379951
10.1002/adsc.201600918
10.1021/acs.joc.8b00424
10.1039/c8qo00590g
10.20944/preprints201807.0354.v1
10.1002/ejoc.201701389
ContentType Journal Article
Copyright Copyright © 2021, Shiri et al. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright © 2021, Shiri et al.
Copyright © 2021, Shiri et al. 2021 Shiri et al.
Copyright_xml – notice: Copyright © 2021, Shiri et al. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Copyright © 2021, Shiri et al.
– notice: Copyright © 2021, Shiri et al. 2021 Shiri et al.
DBID AAYXX
CITATION
3V.
7XB
88I
8FE
8FH
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BFMQW
BHPHI
CCPQU
DWQXO
GNUQQ
HCIFZ
LK8
M2P
M7P
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
Q9U
7X8
5PM
DOA
DOI 10.3762/bjoc.17.114
DatabaseName CrossRef
ProQuest Central (Corporate)
ProQuest Central (purchase pre-March 2016)
Science Database (Alumni Edition)
ProQuest SciTech Collection
ProQuest Natural Science Collection
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection (subscription)
ProQuest Central
ProQuest Continental Europe Database (NC LIVE)
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
ProQuest Central Student
SciTech Premium Collection
Biological Sciences
Science Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic
ProQuest Publicly Available Content
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Central
ProQuest One Applied & Life Sciences
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
ProQuest Central (New)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest Science Journals
ProQuest One Academic Eastern Edition
Continental Europe Database
Biological Science Database
ProQuest SciTech Collection
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

CrossRef
Publicly Available Content Database
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1860-5397
EndPage 1628
ExternalDocumentID oai_doaj_org_article_10bebf8ee03244eea135641d14714dc7
PMC8290111
10_3762_bjoc_17_114
GroupedDBID 23N
2WC
53G
5GY
5VS
6J9
88I
8FE
8FH
AAFWJ
AAYXX
ABUWG
ACGFO
ACGOD
ACPRK
ADBBV
ADRAZ
AENEX
AFKRA
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BBNVY
BCNDV
BENPR
BFMQW
BHPHI
BPHCQ
CCPQU
CITATION
CS3
DIK
DU5
DWQXO
EBS
F5P
GNUQQ
GROUPED_DOAJ
GX1
HCIFZ
HH5
HYE
IAO
IHR
KQ8
LK8
M2P
M48
M7P
M~E
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RNS
RPM
TR2
WOQ
XSB
~9O
3V.
7XB
8FK
PKEHL
PQEST
PQGLB
PQUKI
PRINS
Q9U
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c452t-cfcf74a231311eaa8ca5485bb63d5fd675b62cf92ede56896f1565763aa895dd3
IEDL.DBID BENPR
ISSN 1860-5397
2195-951X
IngestDate Wed Aug 27 01:31:47 EDT 2025
Thu Aug 21 18:32:56 EDT 2025
Thu Jul 10 20:21:33 EDT 2025
Fri Jul 25 10:34:55 EDT 2025
Tue Jul 01 00:54:05 EDT 2025
Thu Apr 24 23:02:10 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
License https://creativecommons.org/licenses/by/4.0
The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms/terms)
This is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c452t-cfcf74a231311eaa8ca5485bb63d5fd675b62cf92ede56896f1565763aa895dd3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ORCID 0000-0003-0071-6570
0000-0002-7034-3071
OpenAccessLink https://www.proquest.com/docview/2595280008?pq-origsite=%requestingapplication%
PMID 34354770
PQID 2595280008
PQPubID 2045588
PageCount 29
ParticipantIDs doaj_primary_oai_doaj_org_article_10bebf8ee03244eea135641d14714dc7
pubmedcentral_primary_oai_pubmedcentral_nih_gov_8290111
proquest_miscellaneous_2559427233
proquest_journals_2595280008
crossref_primary_10_3762_bjoc_17_114
crossref_citationtrail_10_3762_bjoc_17_114
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2021-07-13
PublicationDateYYYYMMDD 2021-07-13
PublicationDate_xml – month: 07
  year: 2021
  text: 2021-07-13
  day: 13
PublicationDecade 2020
PublicationPlace Frankfurt am Main
PublicationPlace_xml – name: Frankfurt am Main
– name: Trakehner Str. 7-9, 60487 Frankfurt am Main, Germany
PublicationTitle Beilstein journal of organic chemistry
PublicationYear 2021
Publisher Beilstein-Institut zur Föerderung der Chemischen Wissenschaften
Beilstein-Institut
Publisher_xml – name: Beilstein-Institut zur Föerderung der Chemischen Wissenschaften
– name: Beilstein-Institut
References ref13
ref57
ref12
ref56
ref15
ref59
ref14
ref58
ref53
ref52
ref11
ref55
ref10
ref54
ref17
ref16
ref19
ref18
ref51
ref50
ref46
ref45
ref48
ref47
ref42
ref41
ref44
ref43
ref49
ref8
ref7
ref9
ref4
ref3
ref6
ref5
ref40
ref35
ref34
ref37
ref31
ref30
ref33
ref32
ref2
ref1
ref39
ref38
Şerban (ref28) 2016; 64
ref24
ref68
ref23
ref67
ref26
ref25
ref20
ref64
ref63
ref22
ref66
ref21
ref65
ref27
ref29
ref60
ref62
Shneine (ref36) 2016; 5
ref61
References_xml – ident: ref12
  doi: 10.1021/acs.accounts.9b00549
– ident: ref61
  doi: 10.1002/adsc.201601388
– ident: ref66
  doi: 10.1016/j.jorganchem.2019.06.013
– ident: ref31
  doi: 10.1002/ejoc.202000999
– ident: ref37
  doi: 10.1021/cr900107r
– ident: ref39
  doi: 10.1039/c9gc01129c
– ident: ref9
  doi: 10.1007/s10562-017-2173-7
– ident: ref15
  doi: 10.1021/jacs.9b09330
– ident: ref26
  doi: 10.1021/acsomega.9b01285
– ident: ref49
  doi: 10.1002/chem.202003386
– ident: ref7
  doi: 10.2174/0929867327666200219141652
– ident: ref50
  doi: 10.1002/adsc.201800394
– ident: ref30
  doi: 10.1002/chem.201601703
– ident: ref35
  doi: 10.1080/00304948.2011.593999
– ident: ref11
  doi: 10.7324/japs.2020.1010016
– ident: ref57
  doi: 10.1021/acs.joc.8b00573
– ident: ref14
  doi: 10.1002/aoc.4974
– ident: ref24
  doi: 10.1039/c7nj04271j
– ident: ref20
  doi: 10.1002/slct.201801905
– ident: ref29
  doi: 10.1021/acs.orglett.9b02269
– ident: ref5
  doi: 10.1039/d0gc00569j
– ident: ref10
  doi: 10.1016/j.ejmech.2014.12.012
– ident: ref65
  doi: 10.1002/chem.201902901
– ident: ref64
  doi: 10.1039/c9ob01175g
– ident: ref25
  doi: 10.1016/j.nurt.2006.11.006
– ident: ref1
  doi: 10.2174/1389557520666201027160436
– ident: ref33
  doi: 10.1016/j.tet.2019.05.046
– ident: ref38
  doi: 10.1007/s41061-015-0001-3
– ident: ref60
  doi: 10.1002/ejoc.201901305
– ident: ref34
  doi: 10.1016/j.ccr.2020.213217
– ident: ref40
  doi: 10.1002/ejoc.201900889
– ident: ref68
  doi: 10.1021/acs.orglett.0c00394
– ident: ref6
  doi: 10.1039/c9sc06377c
– ident: ref17
  doi: 10.1016/j.ejmech.2020.112712
– ident: ref4
  doi: 10.1002/slct.201803418
– ident: ref45
  doi: 10.1002/ajoc.201800340
– ident: ref59
  doi: 10.1002/ejoc.201901249
– ident: ref63
  doi: 10.1016/j.jcat.2019.07.063
– ident: ref62
  doi: 10.1021/acs.joc.8b02916
– ident: ref41
  doi: 10.1039/c9ob01156k
– ident: ref46
  doi: 10.1039/d0ob00848f
– ident: ref16
  doi: 10.3390/molecules24081533
– ident: ref51
  doi: 10.1002/aoc.5319
– ident: ref13
  doi: 10.1016/j.ejmech.2019.07.043
– ident: ref21
  doi: 10.1128/aac.01436-16
– volume: 5
  start-page: 1411
  year: 2016
  ident: ref36
  publication-title: International Journal of Scientific Research
– ident: ref2
  doi: 10.1002/jhet.4174
– ident: ref32
  doi: 10.1002/aoc.5600
– ident: ref47
  doi: 10.1007/s10593-018-2343-6
– ident: ref54
  doi: 10.1016/j.bmcl.2017.11.038
– ident: ref18
  doi: 10.1002/slct.201902362
– ident: ref22
  doi: 10.1016/j.bioorg.2019.103162
– ident: ref43
  doi: 10.1007/s10719-019-09883-1
– ident: ref19
  doi: 10.1002/ardp.202000163
– ident: ref55
  doi: 10.1021/acs.orglett.8b01002
– volume: 64
  start-page: 549
  year: 2016
  ident: ref28
  publication-title: Farmacia (Bucharest, Romania)
– ident: ref44
  doi: 10.1039/c8ob00533h
– ident: ref52
  doi: 10.1002/cjoc.201900556
– ident: ref56
  doi: 10.1021/acs.joc.0c00520
– ident: ref42
  doi: 10.1021/acs.joc.9b01817
– ident: ref48
  doi: 10.1016/j.jddst.2019.101130
– ident: ref3
  doi: 10.1016/j.tet.2017.10.003
– ident: ref8
  doi: 10.1055/s-0034-1379951
– ident: ref27
  doi: 10.1002/adsc.201600918
– ident: ref67
  doi: 10.1021/acs.joc.8b00424
– ident: ref58
  doi: 10.1039/c8qo00590g
– ident: ref23
  doi: 10.20944/preprints201807.0354.v1
– ident: ref53
  doi: 10.1002/ejoc.201701389
SSID ssj0040606
Score 2.4288487
SecondaryResourceType review_article
Snippet Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The...
SourceID doaj
pubmedcentral
proquest
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Enrichment Source
Index Database
StartPage 1600
SubjectTerms 1,4,5-trisubstituted 1,2,3-triazoles
[3 + 2]‐cycloaddition
Azide
azides
Catalysis
Chemistry
click reaction
fully functionalized 1,2,3-triazoles
n-containing heterocycles
Review
Triazoles
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NS91AEF-KF3sp1baY-sEWPJW3NfuZ5KhSEaE9VfAW9mOWWkpSfM-D_vXOJHkPAwUvngKbCWx-k9mZyc7-hrFjqKAJpQNRaW2E8coK72svdBmgzuBdHugYfvx0l9fm6sbePGv1RTVhIz3wCBxadYCQa4ASXb8B8FJbZ2SSuKqaFIdz5Ojz1snUuAajlxq6asralcKiyx1P5qExqZPwp4_fZEUkuTNfNFD2z-LMeZXkM7dz8Z69m-JFfjrOc4e9gW6XbZ-v27R9YFenHBctfJhTMSb96Od9xzGs48uHDi_L2yXvM5cLs7BihSaNK8VYHpBwUC00DfpH4nX6yK4vvv86vxRTgwQRjVUrEXPMFeKriTMHEOPoMQGxITidbE6YCwSnYm4UJLCublyWtMvpNIo2NiX9iW11fQd7jOsI1iQP1ueINp0aH1xF-IJxqYyuYF_XULVxYg-nJhZ_W8wiCNeWcG1lRcecC3a8Ef43kmb8X-yMMN-IENP1MID6byf9ty_pv2AHa421k_ktW8zprKopvinYl81tVAzthvgO-nuSsY1RldK6YNVM07MJze90t78HCu5h-1nKz6_xBvvsraJCGWLr1Adsa3V3D4cY6azC0fBRPwE-wf0I
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Scholars Portal Journals: Open Access
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3da9RAEF9qfdAX8ROjVVbok1zq7XfyIFKLpRTqkwf3FvZjVisl0bsrWP96Z3LJYaT4FNidJWFmZ2cmM_sbxg7BQR3mFkqnlC61l6b0vvKlmgeoMnibeziGi8_2bKHPl2a5x8ZmnAMD17eGdtRParG6Ovr18-YDKvx7ijhRl9-F7108Eo5gb--wu2iSHPVwuNC7dAIarb7JpuwbExqx3F7U-3fxxDT1CP4Tt3NaNPmXFTp9yB4M7iM_3sr7EduD9jG7dzJ2bXvCzo85nmG4mFNtJv33513L0cvj65sWH-vLNe8yFzM9M-UGNRwPjm21QMJBOVM06H8TzNNTtjj99OXkrBz6JZRRG7kpY47ZIbsVQegAsjx6jEdMCFYlkxOGBsHKmGsJCYytapsFJT2tQtLapKSesf22a-E54yqC0cmD8TmiiqfaB-t0ig60TfNoC_Z2ZFUTBzBx6mlx1WBQQXxtiK-NcHTruWCHO-IfWwyN28k-Es93JAR83Q90q6_NoEe4LkDIFcAcPUEN4IUyVosk0MjS9xXsYJRYM26mBkM8Iytydwr2ZjeNgqHkiG-huyYaU2vppFIFcxNJTz5oOtNefusRuftstBAv_v_yl-y-pIoYguVUB2x_s7qGV-jSbMLrfrv-AYRo9wU
  priority: 102
  providerName: Scholars Portal
Title A recent overview on the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles
URI https://www.proquest.com/docview/2595280008
https://www.proquest.com/docview/2559427233
https://pubmed.ncbi.nlm.nih.gov/PMC8290111
https://doaj.org/article/10bebf8ee03244eea135641d14714dc7
Volume 17
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1La9wwEBZtcmgvIX1Rp2lwIaeyblZv-1SSkBACCaU0sDejx6hNKXYSbw7pr8-M197WUHqxQRpheaR5SBp9w9g-WKj83EBhpVSFckIXzpWukHMPZQJnUg_HcHFpzq7U-UIvhg23bgirHHVir6hjG2iP_ADddC1KMlmfb24LyhpFp6tDCo2nbBNVcIkzfPPo5PLL11EXo7Xqs2uKPiOh5ovVDT0UKnHgf7bhE7cEljuxST10_8TfnEZL_mV-TrfZ1uA35oergX7BnkDzkj07HtO1vWLnhzkqL2ycU1Am_UzeNjm6d3n30OCru-7yNuV8pma6WKJoo8ZYhQlELBQzSYXuN-E7vWZXpyffjs-KIVFCEZQWyyKkkCzyWRJ2DiCvg8OFiPbeyKhTxDWBNyKkSkAEbcrKJE6nnUYiaaVjlG_YRtM28JblMoBW0YF2KaBsx8p5Y1UMFpSJ82Ay9nFkVR0GFHFKZvGrxtUE8bUmvtbc0nXnjO2viW9W4Bn_Jjsinq9JCPG6L2jvvteDAGE7Dz6VAHN0ARWA41IbxSNH60r9y9juOGL1IIZd_WfSZOzDuhoHhk5FXAPtPdHoSgkrpMyYnYz0pEPTmub6Rw_F3R9Dc77z_4-_Y88FhcIQHqfcZRvLu3t4j77M0u8NE3av3wvA54UqHwEhUffg
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwzV1Lb9NAEB6V9FAuvFENBYxULihO433ZPnBoC1H6SCWkVuRm9mUoIBs1iVD7V_gr_DhmHDtghLhV4mRpPbbH3tmZb72z3wBs-8RnZqh8lHAuIqGZjLROdcSHxqeF16qo6RgmJ2p8Jg6ncroG39u9MJRW2frE2lG7ytI_8h2E6ZKlFLKaDMojf_kN52ezVwevsTNfMDZ6c7o_jpoSApEVks0jW9giQQ04scp41MJqhOjSGMWdLByiZaOYLTLmnZcqzVQR0zqg4iiaSec43vcGrKcUh3uwvjeavH3XOnoMhXXpTlaXO5TxdLn9D0cs2zGfKjuIE2Li7QS8ui5AB8x2UzF_i22j2_Cj_SrLlJbPg8XcDOzVH4SR_-lnuwO3Gkwd7i4HwV1Y8-U92NhvS9ndh8PdEB07vntICaukcViVIULfcHZZ4mF2PgurIoz7oi-jObo99KbLFAqHjazPqVFfEffVAzi7lld5CL2yKv0mhNx6KZz2UhcW_Z7LtFGJcDbxQrmhVQG8bHs6tw3DOhX6-JLjTIvMIiezyOOEtoIHsL0S_rokFvm72B6ZzEqE2MDrhuriQ944F7zOeFOk3g8RHgvvdcylErGLEXmQfgFstcaRNy5qlv-yjACer05jx9CKkS59tSAZmQmWMM4DSDqG2lGoe6Y8_1jTlNdL9HH86N8PfwYb49PJcX58cHL0GG4yShki3lK-Bb35xcI_Qcw3N0-bsRfC--u225_kLWfu
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lb9NAEB6VVAIuvBGBAkYqFxQn8b5sHxDqg6gPWoFERW5mX4YCskuTCLU_jb_Cn2HGj4AR4tYDp0jrsbNefzvz2Tv7DcC6j31qxsqHMeciFJrJUOtEh3xsfJJ7rfJKjuHgUO0cib2pnK7A93YvDKVVtj6xctSutPSNfIQ0XbKEQtYob9IiXm9PXpx8DamCFK20tuU0aojs-7Nv-Po2e767jc_6KWOTl2-3dsKmwkBohWTz0OY2j7GDnERnPHbSamTw0hjFncwdkmmjmM1T5p2XKklVHtEyoeJomkrnOF73EqwmCnlLD1Y3Jwdv3rVxACNlVdmTVdUQZTStdwfihGYj86m0wygmod5OPKzKBnS4bjdT87fQN7kOP9pBqzNePg8XczO053_oSf6fo3oDrjWMPNiop9BNWPHFLbiy1RbCuw17GwGGBRyagNJd6YaCsgiQOAezswJ_ZsezoMyDaCAGMpyj00RfXCdgOGxkA06N-pyUs-7A0YXcyl3oFWXh70HArZfCaS91btFrulQbFQtnYy-UG1vVh2ctEDLb6LNTmZAvGb6nEWoyQk0WxbSRvA_rS-OTWpbk72abhKilCWmJVw3l6YescU14nvEmT7wfI7kW3uuISyUiFyFvof71Ya3FTtY4uFn2Czh9eLI8jA-G1pt04csF2chUsJhx3oe4g-NOh7pHiuOPlch5tcAfRff__eeP4TLiNXu1e7j_AK4yyjci0VO-Br356cI_RMI4N4-amRnA-4uG7U_TMH_I
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=A+recent+overview+on+the+synthesis+of+1%2C4%2C5-trisubstituted+1%2C2%2C3-triazoles&rft.jtitle=Beilstein+journal+of+organic+chemistry&rft.au=Shiri+Pezhman&rft.au=Amani+Ali+Mohammad&rft.au=Mayer-Gall%2C+Thomas&rft.date=2021-07-13&rft.pub=Beilstein-Institut+zur+F%C3%B6erderung+der+Chemischen+Wissenschaften&rft.issn=2195-951X&rft.eissn=1860-5397&rft.volume=17&rft.spage=1600&rft.epage=1628&rft_id=info:doi/10.3762%2Fbjoc.17.114&rft.externalDBID=HAS_PDF_LINK
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1860-5397&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1860-5397&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1860-5397&client=summon