Stereodivergent conjugate reduction of α-substituted α,β-unsaturated <i>N</i>-sulfinyl ketimines: flexible access to challenging acyclic β,β-disubstituted enesulfinamides-Reference-Cited by-同舟云学术

Stereodivergent conjugate reduction of α-substituted α,β-unsaturated N-sulfinyl ketimines: flexible access to challenging acyclic β,β-disubstituted enesulfinamides

Published:2024 Issue:4 Volume:11 Page:1218-1224
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Yisimayili Nuermaimaiti¹,Liu Tao¹,Xiong Teng-Zhao¹,Lu Chong-Dao¹²^ORCID

Affiliation:

1. School of Chemical Science and Technology, Yunnan University, Kunming, Yunnan 650091, China

2. School of Health, Jiangxi Normal University, Nanchang, Jiangxi 330022, China

Abstract

Stereodivergent 1,4-reduction to provide flexible access to the challenging acyclic enesulfinamides featuring two electronically and sterically similar β-substituents.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO02028B

Reference54 articles.

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4. Catalytic Asymmetric α-Functionalization of α-Branched Aldehydes

5. Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres

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