Efficient Enantioselective Hetero-Diels−Alder Reaction of Brassard's Diene with Aliphatic Aldehydes: A One-Step Synthesis of (R)-(+)-Kavain and (S)-(+)-Dihydrokavain-Reference-Cited by-同舟云学术

Efficient Enantioselective Hetero-Diels−Alder Reaction of Brassard's Diene with Aliphatic Aldehydes: A One-Step Synthesis of (R)-(+)-Kavain and (S)-(+)-Dihydrokavain

Published:2008-02-28 Issue:6 Volume:10 Page:1311-1314
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lin Lili¹,Chen Zhenling¹,Yang Xu¹,Liu Xiaohua¹,Feng Xiaoming¹

Affiliation:

1. Key Laboratory of Green Chemistry & Technology (Sichuan University), Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China, and State Key Laboratory of Oral Diseases, Sichuan University, Chengdu 610041, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol8002282

Reference34 articles.

1. Chiral Hetero Diels−Alder Products by Enantioselective and Diastereoselective Zirconium Catalysis. Scope, Limitation, Mechanism, and Application to the Concise Synthesis of (+)-Prelactone C and (+)-9-Deoxygoniopypyrone

2. Total Synthesis of Phorboxazole B

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