A Diastereoselective Oxa-Pictet–Spengler-Based Strategy for (+)-Frenolicin B and epi-(+)-Frenolicin B Synthesis-Reference-Cited by-同舟云学术

A Diastereoselective Oxa-Pictet–Spengler-Based Strategy for (+)-Frenolicin B and epi-(+)-Frenolicin B Synthesis

Published:2013-10-23 Issue:21 Volume:15 Page:5566-5569
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Yinan¹,Wang Xiachang¹,Sunkara Manjula¹,Ye Qing¹,Ponomereva Larissa V.¹,She Qing-Bai¹,Morris Andrew J.¹,Thorson Jon S.¹

Affiliation:

1. Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, Kentucky 40536, United States, and Division of Cardiovascular Medicine, Gill Heart Institute, and Markey Cancer Center, University of Kentucky, 741 South Limestone Street, Lexington, Kentucky 40536, United States

Funder

NIH Office of the Director

NIH Clinical Center

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol4027649

Reference25 articles.

1. Production of deoxyfrenolicin and a new antibiotic, frenolicin B by Streptomyces roseofulvus strain AM-3867.

2. Anticoccidial activity of frenolicin B and its derivatives.