New Stereoselective Route to the Epoxyquinol Core of Manumycin-Type Natural Products. Synthesis of Enantiopure (+)-Bromoxone, (−)-LL-C10037α, and (+)-KT 8110-Reference-Cited by-同舟云学术

New Stereoselective Route to the Epoxyquinol Core of Manumycin-Type Natural Products. Synthesis of Enantiopure (+)-Bromoxone, (−)-LL-C10037α, and (+)-KT 8110

Published:2000-01-14 Issue:3 Volume:65 Page:716-721
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Block Oliver¹,Klein Georg¹,Altenbach Hans-Josef¹,Brauer David J.¹

Affiliation:

1. Fachbereich Chemie, Bergische Universität-Gesamthochschule Wuppertal, Gauss-trasse 20, D-42097 Wuppertal, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo991324c

Reference28 articles.

1. Structure of Chaloxone, Isolated from a Chalara Sp.

2. New antitumor antibiotic, LL-C10037.ALPHA. fermentation, isolation and structure determination.

3. Structure and absolute stereochemistry of the epoxyquinol LL-C10037.alpha. and related metabolites from Streptomyces LL-C10037

4. The Synthesis of Alisamycin, Nisamycin, LL-C10037α and Novel Epoxyquinol and Epoxyquinone Analogues of Manumycin A

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