Issue 37, 2022

BF3·Et2O-Mediated annulation of α-keto acids with aliphatic ketones for the synthesis of γ-hydroxy-butenolides and γ-alkylidene-butenolides

Abstract

Annulation reaction of α-keto acids with cyclic or acyclic aliphatic ketones is reported herein to divergently access γ-hydroxy-butenolides and γ-alkylidene-butenolides depending on the amount of BF3·Et2O. This protocol features good functional tolerance and ease of operation, to open a route to access butenolides via an annulation and dehydration process.

Graphical abstract: BF3·Et2O-Mediated annulation of α-keto acids with aliphatic ketones for the synthesis of γ-hydroxy-butenolides and γ-alkylidene-butenolides

Supplementary files

Article information

Article type
Paper
Submitted
22 Jul 2022
Accepted
18 Aug 2022
First published
25 Aug 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 24237-24241

BF3·Et2O-Mediated annulation of α-keto acids with aliphatic ketones for the synthesis of γ-hydroxy-butenolides and γ-alkylidene-butenolides

Z. Cheng, Q. Gu, Y. Xie, Y. Zhang and X. Zeng, RSC Adv., 2022, 12, 24237 DOI: 10.1039/D2RA04546J

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