An Efficient Method for Cyclopentene Annulation onto α,β-Unsaturated Ketones: W(CO)5(L)-Catalyzed 5-Endo-Dig Cyclization of 6-Siloxy-5-en-1-ynes-Reference-Cited by-同舟云学术

An Efficient Method for Cyclopentene Annulation onto α,β-Unsaturated Ketones: W(CO)5(L)-Catalyzed 5-Endo-Dig Cyclization of 6-Siloxy-5-en-1-ynes

Published:2002-11-16 Issue:25 Volume:4 Page:4463-4466
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Iwasawa Nobuharu¹,Miura Tomoya¹,Kiyota Koichi¹,Kusama Hiroyuki¹,Lee Kooyeon¹,Lee Phil Ho¹

Affiliation:

1. Department of Chemistry, Tokyo Institute of Technology, O-okayama, Meguro-ku, Tokyo 152-8551, Japan, and Department of Chemistry, Kangwon National University, Chunchon 200-701, Republic of Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol026993i

Reference17 articles.

1. Formal Total Synthesis of (+)-Trehazolin. Application of an Asymmetric Aldol−Olefin Metathesis Approach to the Synthesis of Functionalized Cyclopentenes

2. (Trimethylsilyl)cyclopentene annulation: a regiocontrolled approach to the synthesis of five-membered rings

3. Scope and stereochemical course of the (trimethylsilyl)cyclopentene annulation

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