A Tandem Michael Addition–Rearrangement–Carbonylation by (4-Nitrophenylsulfonylmethyl) Benzene and Its Derivatives with Methacrylates under PTC-Reference-Cited by-同舟云学术

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A Tandem Michael Addition–Rearrangement–Carbonylation by (4-Nitrophenylsulfonylmethyl) Benzene and Its Derivatives with Methacrylates under PTC

Published:2003-09 Issue:9 Volume:2003 Page:559-561
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Yue Guoren¹²,She Xuegong¹,Zhang Zheng³,Pan Xinfu¹

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, 730000, Lanzhou, Gansu, P.R. China

2. Department of Chemistry, Hexi University, 734000, Zhangye, Gansu, P.R. China

3. Nanjing University, 210093, Nanjing, Jiangsu, P.R. China

Abstract

A novel tandem Michael addition–rearrangement–carbonylation was studied in the reaction of (4-nitrophenylsulfonylmethyl)benzene(1) and its derivatives with methacrylates (2) under solid–liquid PTC conditions and a probable mechanism is discussed.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823403322597306

Reference21 articles.

1. Development of sulfur compounds as synthetic reagents

2. Carbanions of 1,3-Dithianes. Reagents for CC Bond Formation by Nucleophilic Displacement and Carbonyl Addition

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Tandem Michael Addition—Rearrangement—Carbonylation by (4-Nitrophenylsulfonylmethyl)benzene and Its Derivatives with Methacrylates under PTC.;ChemInform;2004-04-13

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