Phase-Transfer-Catalyzed Asymmetric Synthesis of Chiral N-Substituted Pyr­azoles by Aza-Michael Reaction

An efficient cinchona‐based phase‐transfer‐catalyzed asymmetric aza‐Michael reaction of pyrazole with various α,β‐unsaturated ketones has been developed for the preparation of chiral N‐substituted pyrazoles. This reaction provided the desired products in good yields (up to 99 %) with excellent enant...

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Bibliographic Details
Published inEuropean journal of organic chemistry Vol. 2015; no. 29; pp. 6495 - 6502
Main Authors Lee, Su-Jeong, Bae, Ju-Yeon, Cho, Chang-Woo
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.09.2015
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
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Summary:An efficient cinchona‐based phase‐transfer‐catalyzed asymmetric aza‐Michael reaction of pyrazole with various α,β‐unsaturated ketones has been developed for the preparation of chiral N‐substituted pyrazoles. This reaction provided the desired products in good yields (up to 99 %) with excellent enantioselectivities (87–94 % ee). In addition, the reaction of 3‐methyl‐1H‐pyrazole, an unsymmetrically substituted pyrazole, was treated with α,β‐unsaturated ketones to afford the corresponding chiral N‐substituted pyrazoles in good yields (up to 99 %) with excellent enantioselectivities (90–92 % ee) and regioisomeric ratios of up to 9:1. The asymmetric synthesis of chiral N‐substituted pyrazoles has been achieved by phase‐transfer‐catalyzed aza‐Michael reactions of pyrazoles with various α,β‐unsaturated ketones.
Bibliography:istex:02BB10A94156D7E02570939F338A495E168314FD
ark:/67375/WNG-11RQTR1D-V
ArticleID:EJOC201500940
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.201500940