Stereocontrolled Synthesis of C1−C17 Fragment of Narasin via a Free Radical-Based Approach-Reference-Cited by-同舟云学术

Stereocontrolled Synthesis of C1−C17 Fragment of Narasin via a Free Radical-Based Approach

Published:2009-12-02 Issue:1 Volume:12 Page:36-39
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Brazeau Jean-François¹,Guilbault Audrey-Anne¹,Kochuparampil Jummey¹,Mochirian Philippe¹,Guindon Yvan¹

Affiliation:

1. Institut de recherches cliniques de Montréal (IRCM), Bio-organic Chemistry, Laboratory, 110 avenue des Pins Ouest, Montréal, Québec, Canada H2W 1R7, Department of Chemistry, Université de Montréal, C.P. 6128, succursale Centre-Ville, Montréal, Québec, Canada H3C 3J7, and Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montréal, Québec, Canada H3A 2K6

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol902414u

Reference31 articles.

1. Studies on the ionophorous antibiotics. IX. The structure of 4-methylsalinomycin (narasin).

2. A New, Efficient Synthesis of the Left Half of Narasin

3. There has been considerable effort toward the synthesis of salinomycin:

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