Toward the stereochemical assignment of euvesperins A and B: total synthesis of the possible structures of the natural products-Reference-Cited by-同舟云学术

Toward the stereochemical assignment of euvesperins A and B: total synthesis of the possible structures of the natural products

Published:2024 Issue: Volume: Page:
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kobayashi Kenichi¹^ORCID,Honma Yusuke²,Tanaka Kosaku²,Suzuki Momoko¹²,Takatori Kazuhiko²^ORCID,Kogen Hiroshi²

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Health Sciences University of Hokkaido, 1757 Kanazawa, Tobetsu, Ishikari, Hokkaido 061-0293, Japan

2. Graduate School of Pharmaceutical Sciences, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan

Abstract

The possible structures of euvesperins A and B were synthesized, suggesting that euvesperin A may be a mixture of the (2R,3R,4S,7S) and (2S,3S,4R,7S) isomers and euvesperin B may be a mixture of the (2R,3S,4S,7S) and (2S,3R,4R,7S) isomers.

Funder

Japan Society for the Promotion of Science

Akiyama Life Science Foundation

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB01118J

Reference16 articles.

1. Euvesperins A and B, new circumventors of arbekacin resistance in MRSA, produced by Metarhizium sp. FKI-7236

2. Metarhizium aciculare sp. nov. for euvesperins A and B producing Metarhizium strains

3. Biverlactones A–D, new circumventors of arbekacin resistance in MRSA, produced by Penicillium sp. FKI-4429

4. Aogacillins A and B Produced by Simplicillium sp. FKI-5985: New Circumventors of Arbekacin Resistance in MRSA

5. Paraphaeosphaeride D and berkleasmin F, new circumventors of arbekacin resistance in MRSA, produced by Paraphaeosphaeria sp. TR-022