Asymmetric and Highly Stereoselective Synthesis of the DEF-Ring Moiety of (−)-FR182877 and Its Derivative Inducing Mitotic Arrest-Reference-Cited by-同舟云学术

Asymmetric and Highly Stereoselective Synthesis of the DEF-Ring Moiety of (−)-FR182877 and Its Derivative Inducing Mitotic Arrest

Published:2012-03-30 Issue:8 Volume:14 Page:2086-2089
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kobayakawa Yu¹,Mori Yusuke¹,Okajima Hideki¹,Terada Yasuhiko¹,Nakada Masahisa¹

Affiliation:

1. Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Waseda University, 3-4-1 Ohkubo, Shinjuku-ku, Tokyo 169-8555, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol300615w

Reference28 articles.

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

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

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

4. Isolation of a Novel Cyclic Hexadepsipeptide Pipalamycin from Streptomyces as an Apoptosis-inducing Agent.

5. FR182876, a New Microtubule Modulator with High Water-solubility, from a Streptomyces

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