Intramolecular 1,3-Dipolar Cycloaddition Strategy for Enantioselective Synthesis of FR-900482 Analogues-Reference-Cited by-同舟云学术

Intramolecular 1,3-Dipolar Cycloaddition Strategy for Enantioselective Synthesis of FR-900482 Analogues

Published:2001-07-10 Issue:16 Volume:3 Page:2575-2578
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kambe Mika¹,Arai Eri¹,Suzuki Masashi¹,Tokuyama Hidetoshi¹,Fukuyama Tohru¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, CREST, The Japan Science and Technology Corporation, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol016243t

Reference13 articles.

1. A new antitumor antibiotic, FR-900482. I. Taxonomic studies on the producing strain: A new species of the genus Streptomyces.

2. FK317, a Novel Substituted Dihydrobenzoxazine, Exhibits Potent Antitumor Activity against Human Tumor Xenografts in Nude Mice

3. DNA Cross-Linking Agents as Antitumor Drugs

4. Enantiospecific synthesis of an aziridinobenzazocinone, an advanced intermediate containing the core nucleus of FR900482 and FK973

5. Synthetic approaches toward FR-900482. I. Stereoselective synthesis of a pentacyclic model compound

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