DTBP‐promoted Passerini‐type reaction of isocyanides with aldehydes: Synthesis of α‐acyloxycarboxamides

A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in...

Full description

Saved in:
Bibliographic Details
Published inJournal of the Chinese Chemical Society (Taipei) Vol. 69; no. 10; pp. 1794 - 1802
Main Authors Wang, Zhuo, Zhang, Yan, Wu, Zi‐Han, Zhao, Yu‐Long
Format Journal Article
LanguageEnglish
Published Weinheim Wiley‐VCH Verlag GmbH & Co. KGaA 01.10.2022
Wiley Subscription Services, Inc
Subjects
aldehyde
Aldehydes
Functional groups
isocyanides
Passerini reaction
α‐acyloxycarboxamides
Online AccessGet full text

Cover

Abstract A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in good to high yields in a single step. The experimental results clearly confirmed the role of water and provided a better mechanistic understanding of this reaction. A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in good to high yields in a single step.
AbstractList A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in good to high yields in a single step. The experimental results clearly confirmed the role of water and provided a better mechanistic understanding of this reaction.
Abstract A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in good to high yields in a single step. The experimental results clearly confirmed the role of water and provided a better mechanistic understanding of this reaction.
A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in good to high yields in a single step. The experimental results clearly confirmed the role of water and provided a better mechanistic understanding of this reaction. A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of isocyanides and aldehydes and provides an efficient method for the synthesis of α‐acyloxycarboxamides with two identical functional groups in good to high yields in a single step.
Author Wu, Zi‐Han
Zhang, Yan
Zhao, Yu‐Long
Wang, Zhuo
Author_xml – sequence: 1
  givenname: Zhuo
  surname: Wang
  fullname: Wang, Zhuo
  organization: Northeast Normal University
– sequence: 2
  givenname: Yan
  surname: Zhang
  fullname: Zhang, Yan
  organization: Northeast Normal University
– sequence: 3
  givenname: Zi‐Han
  surname: Wu
  fullname: Wu, Zi‐Han
  organization: Northeast Normal University
– sequence: 4
  givenname: Yu‐Long
  orcidid: 0000-0001-6577-1074
  surname: Zhao
  fullname: Zhao, Yu‐Long
  email: zhaoyl351@nenu.edu.cn
  organization: Northeast Normal University
BookMark eNqFkEtOwzAURS1UJEphyjgS4xR_YidmBuGvSlRqGUeOY6uu0rjYqdrMWAJbYSMsgpXgqAiGjN5H97yrd4_BoLGNAuAMwTGCEF8spfRjDDEOA4cHYIgRxzGjCR-AIYSQxwkl7Agce7-EMCGY8iFobubX06-397WzK9uqKpoK75UzjQnLtluryCkhW2ObyOrIeCs70ZhK-Whr2kUk6kotujBeRrOuaRfKG98LPz8CLmRX210nhSvtTqx66gQcalF7dfpTR-Dl7naeP8ST5_vH_GoSS5xiGJeqpKFLMpIwxiqeUlRJWFJdCQWxQAgRqDOtaEYyoTHhWcJ0laoS6ZJhlJERON_fDX-9bpRvi6XduCZYFsEgpSwjnAXVeK-SznrvlC7WzqyE6woEiz7Tos-0-M00AHwPbE2tun_UxVOez_7Yb0O6gj0
Cites_doi 10.1002/ejoc.202000016
10.1021/ol0617502
10.3987/COM-07-S(W)50
10.1039/D0QO01095B
10.1039/C3CC49022J
10.1021/cc8000103
10.1039/C5QO00202H
10.1016/S0040-4039(02)00226-5
10.1021/cr900411f
10.1021/cr500380d
10.1021/acs.joc.1c02107
10.1002/adsc.201800445
10.1039/C9CC05802H
10.1039/D0OB01340D
10.1038/s41467-020-20727-7
10.1039/C9QO01229J
10.1016/j.catcom.2020.106118
10.1021/acs.orglett.6b03293
10.1002/anie.202116249
10.2174/1385272824666200110095120
10.1021/acs.joc.8b01842
10.1002/adsc.201400017
10.1002/chem.202003224
10.1021/acs.orglett.9b00307
10.1002/adsc.202000957
10.1021/acs.orglett.8b01462
10.1039/C8RA07150K
10.1002/anie.201905838
10.1021/acs.orglett.8b01561
10.1002/adsc.202001512
10.1039/D0OB02600J
10.1039/C9QO00856J
10.1039/D0QO00994F
10.1002/anie.200705347
10.1021/cr100233r
10.1002/chem.201304618
10.1021/ol500518n
10.1039/C6CC01562J
10.1039/C6GC00910G
10.1021/jo070202e
10.1039/D1SC03810A
10.1021/acs.joc.1c02890
10.1039/C6CS00444J
10.1021/jo900354e
10.1002/anie.200804213
10.1021/ol101763w
10.1039/C6CS00384B
10.1016/S0040-4039(02)01505-8
10.1016/j.tet.2007.10.050
10.1039/D1QO01506K
10.1021/acs.joc.9b02760
10.1039/c3cs35507a
10.1039/D1QO00153A
10.1039/c2cs15361k
10.1039/D0CC00594K
10.1039/D1NJ03832J
10.1021/acs.orglett.0c02835
ContentType Journal Article
Copyright 2022 The Chemical Society Located in Taipei & Wiley‐VCH GmbH.
2022 The Chemical Society Located in Taipei & Wiley‐VCH GmbH
Copyright_xml – notice: 2022 The Chemical Society Located in Taipei & Wiley‐VCH GmbH.
– notice: 2022 The Chemical Society Located in Taipei & Wiley‐VCH GmbH
DBID AAYXX
CITATION
DOI 10.1002/jccs.202200290
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 2192-6549
EndPage 1802
ExternalDocumentID 10_1002_jccs_202200290
JCCS202200290
Genre article
GrantInformation_xml – fundername: Natural Science Foundation of Jilin Province
  funderid: 20190201073JC
– fundername: National Natural Science Foundation of China
  funderid: 21472017; 21871044
GroupedDBID 05W
0R~
1OB
1OC
2NJ
2WC
31~
33P
3SF
50Y
52U
5GY
8-0
8-1
8RM
A00
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCUV
ABDBF
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFO
ACGFS
ACIWK
ACPOU
ACXBN
ACXQS
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
AEEZP
AEGXH
AEIGN
AEIMD
AENEX
AEQDE
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AHBTC
AI.
AIAGR
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ATUGU
AUFTA
AZVAB
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BOGZA
BRXPI
BZXJU
DCZOG
DPXWK
DRFUL
DRSTM
E3Z
EBS
EJD
EOJEC
FEDTE
G-S
GODZA
HGLYW
HH5
HVGLF
HZ~
LATKE
LEEKS
LITHE
LOXES
LUTES
LYRES
MEWTI
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
MY~
O66
O9-
OBODZ
OK1
P2P
P2W
PALCI
Q0C
R.K
RIWAO
RJQFR
ROL
RX1
SAMSI
SUPJJ
TR2
VH1
WBFHL
WBKPD
WIH
WIK
WOHZO
WXSBR
WYISQ
WYJ
ZZTAW
AAYXX
CITATION
ID FETCH-LOGICAL-c2720-beb5c274834666d9751dc0b5fdae02a11130f8fe5838af239846fd7eb1fb62183
ISSN 0009-4536
IngestDate Thu Oct 10 16:40:09 EDT 2024
Fri Aug 23 01:16:45 EDT 2024
Sat Aug 24 00:53:40 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 10
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c2720-beb5c274834666d9751dc0b5fdae02a11130f8fe5838af239846fd7eb1fb62183
Notes Funding information
Natural Science Foundation of Jilin Province, Grant/Award Number: 20190201073JC; National Natural Science Foundation of China, Grant/Award Numbers: 21472017, 21871044
ORCID 0000-0001-6577-1074
PQID 2727568396
PQPubID 2032544
PageCount 9
ParticipantIDs proquest_journals_2727568396
crossref_primary_10_1002_jccs_202200290
wiley_primary_10_1002_jccs_202200290_JCCS202200290
PublicationCentury 2000
PublicationDate October 2022
2022-10-00
20221001
PublicationDateYYYYMMDD 2022-10-01
PublicationDate_xml – month: 10
  year: 2022
  text: October 2022
PublicationDecade 2020
PublicationPlace Weinheim
PublicationPlace_xml – name: Weinheim
– name: Taipei
PublicationTitle Journal of the Chinese Chemical Society (Taipei)
PublicationYear 2022
Publisher Wiley‐VCH Verlag GmbH & Co. KGaA
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley‐VCH Verlag GmbH & Co. KGaA
– name: Wiley Subscription Services, Inc
References 2020 2020 2021 2017 2017 2015 2013 2014; 18 59 8 46 46 115 42 356
2010; 12
2009; 74
2021 2022 2020; 12 46 2020
2016 2007; 18 74
2021; 12
2022 2022 2019 2018 2019 2019; 9 87 84 360 55 84
2008 2002; 47 43
2020 2008 2002; 7 10 43
2021 2021 2020 2020 2020 2020 2019 2019; 363 363 22 7 7 56 21 6
2016 2021 2020 2021 2012 2010 2012; 52 19 24 27 112 110 41
2020; 145
2022; 87
2016; 18
2018 2018; 20 8
2018; 20
2022 2014 2006 2007 2007; 61 50 8 72 63
2008 2014 2015; 47 16 2
2014; 20
e_1_2_6_19_3
e_1_2_6_19_4
e_1_2_6_19_1
e_1_2_6_19_2
e_1_2_6_19_7
e_1_2_6_19_8
e_1_2_6_19_5
e_1_2_6_19_6
e_1_2_6_13_1
e_1_2_6_13_2
e_1_2_6_11_1
e_1_2_6_17_1
e_1_2_6_15_1
e_1_2_6_20_2
e_1_2_6_20_1
e_1_2_6_3_7
e_1_2_6_9_1
e_1_2_6_3_6
e_1_2_6_7_2
e_1_2_6_3_3
e_1_2_6_5_1
e_1_2_6_3_2
e_1_2_6_3_5
e_1_2_6_7_1
e_1_2_6_3_4
e_1_2_6_5_2
e_1_2_6_20_6
e_1_2_6_20_5
e_1_2_6_3_1
e_1_2_6_20_4
e_1_2_6_20_3
e_1_2_6_10_1
e_1_2_6_18_2
e_1_2_6_18_3
e_1_2_6_14_1
e_1_2_6_12_1
e_1_2_6_18_1
e_1_2_6_14_2
e_1_2_6_14_3
e_1_2_6_16_1
e_1_2_6_8_5
e_1_2_6_2_8
e_1_2_6_8_2
e_1_2_6_2_7
e_1_2_6_8_1
e_1_2_6_8_4
e_1_2_6_8_3
e_1_2_6_2_4
e_1_2_6_4_2
e_1_2_6_2_3
e_1_2_6_4_1
e_1_2_6_2_6
e_1_2_6_2_5
e_1_2_6_4_3
e_1_2_6_6_1
e_1_2_6_2_2
e_1_2_6_2_1
References_xml – volume: 20
  start-page: 3988
  year: 2018
  publication-title: Org. Lett.
– volume: 12
  start-page: 441
  year: 2021
  publication-title: Nat. Commun.
– volume: 12 46 2020
  start-page: 1445 3766
  year: 2021 2022 2020
  publication-title: Chem. Sci. New J. Chem. Eur. J. Org. Chem.
– volume: 61 50 8 72 63
  start-page: 2214 5021 4169
  year: 2022 2014 2006 2007 2007
  publication-title: Angew. Chem. Int. Ed. Chem. Commun. Org. Lett. J. Org. Chem. Tetrahedron.
– volume: 12
  start-page: 4341
  year: 2010
  publication-title: Org. Lett.
– volume: 363 363 22 7 7 56 21 6
  start-page: 1923 244 7640 126 3493 7665 2973 3657
  year: 2021 2021 2020 2020 2020 2020 2019 2019
  publication-title: Adv. Synth. Catal. Adv. Synth. Catal. Org. Lett. Org. Chem. Front. Org. Chem. Front. Chem. Commun. Org. Lett. Org. Chem. Front.
– volume: 9 87 84 360 55 84
  start-page: 407 3156 53 2945
  year: 2022 2022 2019 2018 2019 2019
  publication-title: Org. Chem. Front. J. Org. Chem. J. Org. Chem. Adv. Synth. Catal. Chem. Commun. J. Org. Chem.
– volume: 87
  start-page: 2301
  year: 2022
  publication-title: J. Org. Chem.
– volume: 47 43
  start-page: 9454 6833
  year: 2008 2002
  publication-title: Angew. Chem. Int. Ed. Tetrahedron Lett.
– volume: 47 16 2
  start-page: 2849 1964 1326
  year: 2008 2014 2015
  publication-title: Angew. Chem. Int. Ed. Org. Lett. Org. Chem. Front.
– volume: 18 59 8 46 46 115 42 356
  start-page: 6467 540 3525 1103 1295 2698 5257 2135
  year: 2020 2020 2021 2017 2017 2015 2013 2014
  publication-title: Org. Biomol. Chem. Angew. Chem. Int. Ed. Org. Chem. Front. Chem. Soc. Rev. Chem. Soc. Rev. Chem. Rev. Chem. Soc. Rev. Adv. Synth. Catal.
– volume: 145
  year: 2020
  publication-title: Catal. Commun.
– volume: 7 10 43
  start-page: 3720 507 2293
  year: 2020 2008 2002
  publication-title: Org. Chem. Front. J. Comb. Chem. Tetrahedron Lett.
– volume: 18
  start-page: 6396
  year: 2016
  publication-title: Org. Lett.
– volume: 74
  start-page: 3927
  year: 2009
  publication-title: J. Org. Chem.
– volume: 52 19 24 27 112 110 41
  start-page: 6958 3318 162 6598 3083 5235 3969
  year: 2016 2021 2020 2021 2012 2010 2012
  publication-title: Chem. Commun. Org. Biomol. Chem. Curr. Org. Chem. Chem. Eur. J. Chem. Rev. Chem. Rev. Chem. Soc. Rev.
– volume: 20 8
  start-page: 3875
  year: 2018 2018
  publication-title: Org. Lett. RSC Adv.
– volume: 20
  start-page: 5007
  year: 2014
  publication-title: Chem. Eur. J.
– volume: 18 74
  start-page: 3718 661
  year: 2016 2007
  publication-title: Green Chem. Heterocycles.
– ident: e_1_2_6_4_3
  doi: 10.1002/ejoc.202000016
– ident: e_1_2_6_8_3
  doi: 10.1021/ol0617502
– ident: e_1_2_6_7_2
  doi: 10.3987/COM-07-S(W)50
– ident: e_1_2_6_14_1
  doi: 10.1039/D0QO01095B
– ident: e_1_2_6_8_2
  doi: 10.1039/C3CC49022J
– ident: e_1_2_6_14_2
  doi: 10.1021/cc8000103
– ident: e_1_2_6_18_3
  doi: 10.1039/C5QO00202H
– ident: e_1_2_6_14_3
  doi: 10.1016/S0040-4039(02)00226-5
– ident: e_1_2_6_3_6
  doi: 10.1021/cr900411f
– ident: e_1_2_6_2_6
  doi: 10.1021/cr500380d
– ident: e_1_2_6_16_1
  doi: 10.1021/acs.joc.1c02107
– ident: e_1_2_6_20_4
  doi: 10.1002/adsc.201800445
– ident: e_1_2_6_20_5
  doi: 10.1039/C9CC05802H
– ident: e_1_2_6_2_1
  doi: 10.1039/D0OB01340D
– ident: e_1_2_6_17_1
  doi: 10.1038/s41467-020-20727-7
– ident: e_1_2_6_19_4
  doi: 10.1039/C9QO01229J
– ident: e_1_2_6_15_1
  doi: 10.1016/j.catcom.2020.106118
– ident: e_1_2_6_9_1
  doi: 10.1021/acs.orglett.6b03293
– ident: e_1_2_6_8_1
  doi: 10.1002/anie.202116249
– ident: e_1_2_6_3_3
  doi: 10.2174/1385272824666200110095120
– ident: e_1_2_6_20_3
  doi: 10.1021/acs.joc.8b01842
– ident: e_1_2_6_2_8
  doi: 10.1002/adsc.201400017
– ident: e_1_2_6_3_4
  doi: 10.1002/chem.202003224
– ident: e_1_2_6_19_7
  doi: 10.1021/acs.orglett.9b00307
– ident: e_1_2_6_19_2
  doi: 10.1002/adsc.202000957
– ident: e_1_2_6_13_1
  doi: 10.1021/acs.orglett.8b01462
– ident: e_1_2_6_13_2
  doi: 10.1039/C8RA07150K
– ident: e_1_2_6_2_2
  doi: 10.1002/anie.201905838
– ident: e_1_2_6_11_1
  doi: 10.1021/acs.orglett.8b01561
– ident: e_1_2_6_19_1
  doi: 10.1002/adsc.202001512
– ident: e_1_2_6_3_2
  doi: 10.1039/D0OB02600J
– ident: e_1_2_6_19_8
  doi: 10.1039/C9QO00856J
– ident: e_1_2_6_19_5
  doi: 10.1039/D0QO00994F
– ident: e_1_2_6_18_1
  doi: 10.1002/anie.200705347
– ident: e_1_2_6_3_5
  doi: 10.1021/cr100233r
– ident: e_1_2_6_6_1
  doi: 10.1002/chem.201304618
– ident: e_1_2_6_18_2
  doi: 10.1021/ol500518n
– ident: e_1_2_6_3_1
  doi: 10.1039/C6CC01562J
– ident: e_1_2_6_7_1
  doi: 10.1039/C6GC00910G
– ident: e_1_2_6_8_4
  doi: 10.1021/jo070202e
– ident: e_1_2_6_4_1
  doi: 10.1039/D1SC03810A
– ident: e_1_2_6_20_2
  doi: 10.1021/acs.joc.1c02890
– ident: e_1_2_6_2_5
  doi: 10.1039/C6CS00444J
– ident: e_1_2_6_12_1
  doi: 10.1021/jo900354e
– ident: e_1_2_6_5_1
  doi: 10.1002/anie.200804213
– ident: e_1_2_6_10_1
  doi: 10.1021/ol101763w
– ident: e_1_2_6_2_4
  doi: 10.1039/C6CS00384B
– ident: e_1_2_6_5_2
  doi: 10.1016/S0040-4039(02)01505-8
– ident: e_1_2_6_8_5
  doi: 10.1016/j.tet.2007.10.050
– ident: e_1_2_6_20_1
  doi: 10.1039/D1QO01506K
– ident: e_1_2_6_20_6
  doi: 10.1021/acs.joc.9b02760
– ident: e_1_2_6_2_7
  doi: 10.1039/c3cs35507a
– ident: e_1_2_6_2_3
  doi: 10.1039/D1QO00153A
– ident: e_1_2_6_3_7
  doi: 10.1039/c2cs15361k
– ident: e_1_2_6_19_6
  doi: 10.1039/D0CC00594K
– ident: e_1_2_6_4_2
  doi: 10.1039/D1NJ03832J
– ident: e_1_2_6_19_3
  doi: 10.1021/acs.orglett.0c02835
SSID ssj0043259
Score 2.3300467
Snippet A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide range of...
Abstract A novel DTBP‐promoted Passerini‐type reaction of isocyanides with two molecular aldehydes has been developed. This reaction is applicable for a wide...
SourceID proquest
crossref
wiley
SourceType Aggregation Database
Publisher
StartPage 1794
SubjectTerms aldehyde
Aldehydes
Functional groups
isocyanides
Passerini reaction
α‐acyloxycarboxamides
Title DTBP‐promoted Passerini‐type reaction of isocyanides with aldehydes: Synthesis of α‐acyloxycarboxamides
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjccs.202200290
https://www.proquest.com/docview/2727568396
Volume 69
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NbtNAEF6F9ACXir-KlIJ8oOJkcOz1GnNr3ERRFUqlOmroxVqv16orsKMSSw0nHoFX4UU4c-ZJmLG9G0cEKBziOLvxRtn5PP5mdnaGkGeWSISf9qnpyT43KXNAD6YWN6WgjDJmOb5AP-SbYzae0qOZO-t0vreilspF_EJ82riv5H-kCm0gV9wl-w-S1YNCA5yDfOEIEobjjWR8GA5OdLTCvAqsA_54wnGJPcsz3VX5WYEdCkUPM5DJkudZItXutveJvFgmdYDc6TIHWthkKtkPhvuDvh6KC7Dwr5eCX8XFNf-AI_yG3yKjxerc8iO-N2kJVJAo8NqQZ3OZtTwRZ43r-vyiLH7xZ79bofh89cfGoJ3OSq25St0xwRJKcHHR9mqAQazi426qO9eUum9S12kyaldtoIdtk7l1NlSl6OuaMArQVktto1ZqUQDMirfx8VKnq70UAhO92xjfUtc6Xc_jffw2Gk0nkygczsJbZMv2fNftkq2DweFgpFgCdWzX11X-qiX0neYXXq6Pv06YVlZQ25aqyFB4l2w3UjYOakjeIx2Z3ye3A1U88AHJEZo_Pn9RoDQ0KKER4WgoOBpFarTgaCAcDQ3H14YGI37x21e4fAMEH5LpaBgGY7Mp7WEKXPg3Yxm7cIaebLCfE99z-4mwYjdNuLRsDg9gx0pfpRIX9XmKOSopSxMPiEUaM2T1O6SbF7l8RIw0Bs7vWUkML-ow3-fUk4xzR3o22Aa8R56r-YvmdQaXqM7VbUc405Ge6R7ZU9MbNXc59HpYIAHMCNYjdjXlfxklOgqCU_1p989jPiZ3VujfI93FVSmfAMtdxE8bwPwEESmnGg
link.rule.ids 315,786,790,27955,27956
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=DTBP%E2%80%90promoted+Passerini%E2%80%90type+reaction+of+isocyanides+with+aldehydes%3A+Synthesis+of+%CE%B1%E2%80%90acyloxycarboxamides&rft.jtitle=Journal+of+the+Chinese+Chemical+Society+%28Taipei%29&rft.au=Wang%2C+Zhuo&rft.au=Zhang%2C+Yan&rft.au=Zi%E2%80%90Han+Wu&rft.au=Yu%E2%80%90Long+Zhao&rft.date=2022-10-01&rft.pub=Wiley+Subscription+Services%2C+Inc&rft.issn=0009-4536&rft.eissn=2192-6549&rft.volume=69&rft.issue=10&rft.spage=1794&rft.epage=1802&rft_id=info:doi/10.1002%2Fjccs.202200290&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0009-4536&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0009-4536&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0009-4536&client=summon