Total Synthesis and Determination of the Absolute Configuration of Naturally Occurring Mangromicin A, with Potent Antitrypanosomal Activity-Reference-Cited by-同舟云学术

Total Synthesis and Determination of the Absolute Configuration of Naturally Occurring Mangromicin A, with Potent Antitrypanosomal Activity

Published:2016-12-12 Issue:1 Volume:19 Page:230-233
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Takada Hirokazu¹,Yamada Takeshi¹,Hirose Tomoyasu¹,Ishihara Takuma¹,Nakashima Takuji¹,Takahashi Yo̅ko¹,O̅mura Satoshi¹,Sunazuka Toshiaki¹^ORCID

Affiliation:

1. Graduate School of Infection Control Sciences and Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan

Funder

Eisai

Sumitomo Foundation

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b03512

Reference18 articles.

1. Mangromicins A and B: structure and antitrypanosomal activity of two new cyclopentadecane compounds from Lechevalieria aerocolonigenes K10-0216

2. Mangromicin C, a new analog of mangromicin

3. O̅mura, S.; Takahashi, Y.; Nakashima, T.; Otoguro, K.; Shiomi, K.; Iwatsuki, M.; Matsumoto, A.WO2013031239, Japan, 2013–03–07.

4. Akaeolide, a Carbocyclic Polyketide from Marine-Derived Streptomyces

5. The vinylogous Mukaiyama aldol reaction (VMAR) in natural product synthesis

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