Highly Stereoselective Synthesis of 2,5-Disubstituted 3-Vinylidene Tetetrahydrofurans via Prins-Type Cyclization-Reference-Cited by-同舟云学术

Highly Stereoselective Synthesis of 2,5-Disubstituted 3-Vinylidene Tetetrahydrofurans via Prins-Type Cyclization

Published:2005-06-18 Issue:15 Volume:7 Page:3283-3285
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shin Chul¹,Chavre Satish N.¹,Pae Ae Nim¹,Cha Joo Hwan¹,Koh Hun Yeong¹,Chang Moon Ho¹,Choi Jung Hoon¹,Cho Yong Seo¹

Affiliation:

1. Biochemicals Research Center, Korea Institute of Science and Technology, P.O. Box 131, Cheongryang, Seoul 130-650, Korea, and Department of Chemistry, Hanyang University, 17 Haengdang-Dong, Sungdong-Gu, Seoul, 133-791, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol051058r

Reference38 articles.

1. Stereoselective Synthesis of Tetrahydrofurans via the Palladium-Catalyzed Reaction of Aryl Bromides with γ-Hydroxy Alkenes: Evidence for an Unusual Intramolecular Olefin Insertion into a Pd(Ar)(OR) Intermediate

2. Anodic Coupling Reactions: Probing the Stereochemistry of Tetrahydrofuran Formation. A Short, Convenient Synthesis of Linalool Oxide

3. A convenient synthesis of substituted 3-bromotetrahydrofurans from homoallylic alcohols

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