Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition-Reference-Cited by-同舟云学术

Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition

Published:2016 Issue:30 Volume:52 Page:5269-5272
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Mao Wenbin¹²³⁴⁵,Zhu Chen¹²³⁴⁵

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province

2. College of Chemistry

3. Chemical Engineering and Materials Science

4. Soochow University

5. Suzhou

Abstract

A BF₃-catalyzed, practical synthesis of highly functionalized γ-hydroxybutenolides with a 100% atom efficiency is described.

Funder

National Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C6CC01554A

Reference27 articles.

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2. Anti-inflammatory metabolites from marine sponges

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5. Cacospongionolide B, a New Sesterterpene from the Sponge Fasciospongia cavernosa

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