Synthetic studies on FR182877: an asymmetric synthesis of the AB ring moiety of FR182877 via a diastereoselective intramolecular Diels

Synthetic studies on FR182877: an asymmetric synthesis of the AB ring moiety of FR182877 via a diastereoselective intramolecular Diels–Alder reaction

Published:2002-04 Issue:18 Volume:43 Page:3263-3267
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Suzuki Takahiro,Nakada Masahisa

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Muramatsu, H.; Miyauchi, M.; Sato, B.; Yoshimura, S.; Takase, S.; Terano, H.; Oku, T. 40th Symposium on the Chemistry of Natural Products, Fukuoka, Japan, 1998, Paper 83, pp. 487–492.

2. A New Antimitotic Substance, FR182877. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Biological Activities.

3. A New Antimitotic Substance, FR182877. II. The Mechanism of Action.

4. A New Antimitotic Substance, FR182877. III. Structure Determination.

5. Hexacyclinic acid, a Polyketide fromStreptomyces with a Novel Carbon Skeleton

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