Thiomaleic Anhydride: A Convenient Building Block for the Synthesis of α-Substituted γ- and δ-Lactones through Free-Radical Addition, Nucleophilic Ring Opening, and Subsequent Thiocarboxylate Manipulation-Reference-Cited by-同舟云学术

Thiomaleic Anhydride: A Convenient Building Block for the Synthesis of α-Substituted γ- and δ-Lactones through Free-Radical Addition, Nucleophilic Ring Opening, and Subsequent Thiocarboxylate Manipulation

Published:2009-08-11 Issue:17 Volume:74 Page:6792-6796
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Crich David¹²,Rahaman Md. Yeajur²

Affiliation:

1. Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles, Avenue de la Terrasse, 91198 Gif-sur-Yvette, France

2. Chemistry Department, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo901219k

Reference34 articles.

1. Radikalische Addition an cyclische Derivate der Maleinsäure

2. Cyclic Thioanhydrides: Linchpins for Multicomponent Coupling Reactions Based on the Reaction of Thioacids with Electron-Deficient Sulfonamides and Azides

3. One-Pot Syntheses of Dissymmetric Diamides Based on the Chemistry of Cyclic Monothioanhydrides. Scope and Limitations and Application to the Synthesis of Glycodipeptides

4. A simple synthesis of 2,2-disubstituted tetrahydrothiophenes

5. A convenient and highly chemoselective method for the reductive acetylation of azides

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