Synthesis of 3-Iodoquinolines by Copper-Catalyzed Tandem Annulation from Diaryliodoniums, Nitriles, and 1-Iodoalkynes

A novel method for the synthesis of 3‐iodoquinolines was developed by copper‐catalyzed tandem annulation from diaryliodoniums, nitriles, and 1‐iodoalkynes. It is a method that is characterized by the most convenient operation and wide molecular diversity.

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Bibliographic Details
Published inAdvanced synthesis & catalysis Vol. 358; no. 14; pp. 2332 - 2339
Main Authors Wang, Xuesong, Wang, Xingyong, Huang, Dayun, Liu, Chulong, Wang, Xinyan, Hu, Yuefei
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 14.07.2016
WILEY‐VCH Verlag
Wiley
Subjects
1-iodoalkynes
annulation
Catalysis
Chemical reactions
Chemistry
Chemistry, Applied
Chemistry, Organic
copper catalysts
iodoniums
Nitriles
Organic chemistry
Physical Sciences
Science & Technology
Synthesis
synthesis of quinolones
tandem reactions
ELECTROPHILIC CYCLIZATION
PALLADIUM
1-iodoalkynes
iodoniums
ONE-POT SYNTHESIS
synthesis of quinolones
3-HALOQUINOLINES
ORGANIC AZIDES
ALKYNES
annulation
REGIOSELECTIVE SYNTHESIS
OPTIMIZATION
copper catalysts
DERIVATIVES
tandem reactions
SUBSTITUTED QUINOLINES
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Summary:A novel method for the synthesis of 3‐iodoquinolines was developed by copper‐catalyzed tandem annulation from diaryliodoniums, nitriles, and 1‐iodoalkynes. It is a method that is characterized by the most convenient operation and wide molecular diversity.
Bibliography:ark:/67375/WNG-KTKCD7Q7-S
istex:34973D558FCD9FA9B77058D1C7455971695F45AE
National Natural Scientific Foundation of China - No. Nos. 21372142 and 21472107
ArticleID:ADSC201600081
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1615-4150
1615-4169
DOI:10.1002/adsc.201600081