Issue 5, 2022

A chiral aldehyde-induced tandem conjugated addition–lactamization reaction for constructing fully substituted pyroglutamic acids

Abstract

A catalytic asymmetric tandem reaction including a chiral aldehyde catalyzed conjugated addition and an intramolecular lactamization is reported in this work. Under the optimal reaction conditions, various fully substituted pyroglutamic acids bearing three vicinal chiral centers were generated in good-to-excellent yields and stereoselectivities. A reasonable reaction mechanism is proposed to illustrate the observed stereoselective control results.

Graphical abstract: A chiral aldehyde-induced tandem conjugated addition–lactamization reaction for constructing fully substituted pyroglutamic acids

Supplementary files

Article information

Article type
Research Article
Submitted
27 Dec 2021
Accepted
26 Jan 2022
First published
27 Jan 2022

Org. Chem. Front., 2022,9, 1422-1426

A chiral aldehyde-induced tandem conjugated addition–lactamization reaction for constructing fully substituted pyroglutamic acids

W. Wang, H. Shen, J. Liao, W. Wen and Q. Guo, Org. Chem. Front., 2022, 9, 1422 DOI: 10.1039/D1QO01923F

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