Regioselective α-addition of vinylogous α-ketoester enolate in organocatalytic asymmetric Michael reactions: enantioselective synthesis of Rauhut–Currier type products-Reference-Cited by-同舟云学术

Regioselective α-addition of vinylogous α-ketoester enolate in organocatalytic asymmetric Michael reactions: enantioselective synthesis of Rauhut–Currier type products

Published:2022 Issue:49 Volume:12 Page:32056-32060
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Weng Zhibing¹²,Zhou Ying³,Yue Xin³,Jiang Feng³,Guo Wengang³^ORCID

Affiliation:

1. School of Chemical and Pharmaceutical Engineering, Changzhou Vocational Institute of Engineering, Changzhou, China

2. School of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, China

3. School of Petrochemical Engineering, Changzhou University, Changzhou, China

Abstract

Catalytic asymmetric α-regioselective Michael additions of vinylogous α-ketoester enolate are described herein.

Funder

Changzhou University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA06416B

Reference72 articles.

1. The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress

2. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver

3. Catalysis of the Michael Reaction and the Vinylogous Michael Reaction by Ferric Chloride Hexahydrate

4. The First Enantioselective Organocatalytic Mukaiyama−Michael Reaction: A Direct Method for the Synthesis of Enantioenriched γ-Butenolide Architecture

5. A new methodology for the stereoselective synthesis of 4-substituted butenolides: Asymmetric Michael addition reaction of 2-(trimethylsilyloxy)furans to oxazolidinone enoates

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Progress in catalytic asymmetric α-functionalization of vinylogous nucleophilic species;Organic Chemistry Frontiers;2023