Electrochemical sulfinylation-driven skeletal rearrangement of Baylis–Hillman adducts

Green Chemistry 2026

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Authors: Indrajit Karmakar, Xiangwei Huang, Hsiu-Te Hung, Rekha Bai, Ci‐Yang Sun, Chien‐Wei Chiang, Chin‐Fa Lee
DOI: 10.1039/d5gc05810d
Cited by: 4
References: 64

Abstract

We report an electrochemical sulfinylation protocol that drives a skeletal rearrangement of Baylis–Hillman adducts, enabling the late-stage synthesis of methyl ( Z )-3-(aryl/heteroaryl)-2-[(aryl/alkyl)sulfinyl]methyl acrylates.

Fields of Study & Subjects

Sulfur-Based Synthesis Techniques Synthesis of heterocyclic compounds Catalytic C–H Functionalization Methods

Publication details

Journal / source
Green Chemistry
Publisher
Royal Society of Chemistry (RSC)
Volume
28
Issue
4
Pages
2109–2122
Publication date
1 January 2026
Language
EN