Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Regular Article
Total Synthesis and Biological Evaluation of Prealnumycin B
Kei Kitamura Tatsuro YoneyamaMasaaki NojiHiroto Kaku
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2025 Volume 73 Issue 8 Pages 707-712

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Abstract

Prealnumycin B is an aromatic polyketide characterized as a reduced form of prealnumycin with a 6S-alcohol. As an extension of our earlier work on the synthesis of prealnumycin, the C7–C8 double bond was hydrogenated using Wilkinson’s catalyst, and the C6 carbonyl group was stereoselectively reduced via asymmetric transfer hydrogenation with the (S,S)-Ts-DENEB catalyst, where the use of methanol as a solvent was crucial for achieving high regioselectivity. By comparing its spectroscopic data with those of the natural isolate, the absolute configuration of prealnumycin B was determined to be 1R,6S. In addition, the antibacterial activities of prealnumycin B and related compounds were evaluated.

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Published by The Pharmaceutical Society of Japan

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