Issue 63, 2021, Issue in Progress

Phosphine-catalyzed [3 + 2] annulation of β-sulfonamido-substituted enones with trans-α-cyano-α,β-unsaturated ketones for the synthesis of highly substituted pyrrolidines

Abstract

To synthesize highly substituted pyrrolidines, we developed a phosphine-catalyzed [3 + 2] annulation of β-sulfonamido-substituted enones with trans-α-cyano-α,β-unsaturated ketones. We prepared a series of pyrrolidines under mild conditions with high yields and moderate-to-good diastereoselectivities. A catalytic mechanism for this reaction is suggested.

Graphical abstract: Phosphine-catalyzed [3 + 2] annulation of β-sulfonamido-substituted enones with trans-α-cyano-α,β-unsaturated ketones for the synthesis of highly substituted pyrrolidines

Supplementary files

Article information

Article type
Paper
Submitted
26 Oct 2021
Accepted
09 Dec 2021
First published
17 Dec 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 40136-40139

Phosphine-catalyzed [3 + 2] annulation of β-sulfonamido-substituted enones with trans-α-cyano-α,β-unsaturated ketones for the synthesis of highly substituted pyrrolidines

Z. Gao, L. Xie, L. Ji, X. Ma, X. Li, H. Liu and H. Guo, RSC Adv., 2021, 11, 40136 DOI: 10.1039/D1RA07881J

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