Common synthetic strategy for optically active cyclic terpenoids having a 1,1,5-trimethyl-trans-decalin nucleus: syntheses of (+)-acuminolide, (−)-spongianolide A, and (+)-scalarenedial-Reference-Cited by-同舟云学术

Common synthetic strategy for optically active cyclic terpenoids having a 1,1,5-trimethyl-trans-decalin nucleus: syntheses of (+)-acuminolide, (−)-spongianolide A, and (+)-scalarenedial

Published:2001-10 Issue:40 Volume:57 Page:8425-8442
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Furuichi Noriyuki,Hata Toshiyuki,Soetjipto Hartati,Kato Mariko,Katsumura Shigeo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference44 articles.

1. Synthesis of (−)-Warburganal and 4α-methoxycarbonyl congener from 1-abietic acid

2. The olefin metathesis/transannular ene sequence: a method for the stereocontrolled synthesis of -decalin derivatives. 3. total synthesis of (±)-warburganal

3. A new stereoselective approach for the total synthesis of (.+-.)-isotadeonal, (.+-.)-polygodial, (.+-.)-warburganal, and (.+-.)-muzigadial

4. Total synthesis of (.+-.)-forskolin

5. Using the Principles of ORGANIC CHEMISTRY to Explore CELL BIOLOGY

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