Concise Synthesis of a Lactonamycin Model System by Diastereoselective Dihydroxylation of a Highly Functionalized Naphthoquinone-Reference-Cited by-同舟云学术

Concise Synthesis of a Lactonamycin Model System by Diastereoselective Dihydroxylation of a Highly Functionalized Naphthoquinone

Published:2001-08-07 Issue:18 Volume:3 Page:2899-2902
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Cox Christopher¹,Danishefsky Samuel J.¹

Affiliation:

1. Department of Chemistry, Columbia University, Havemeyer Hall, New York, New York 10027, and Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, Box 106, New York, New York 10021

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol016361g

Reference17 articles.

1. Lactonamycin, a New Antimicrobial Antibiotic Produced by Streptomyces rishiriensis MJ773-88K4. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Biological Activities.

2. Lactonamycin, a New Antimicrobial Antibiotic Produced by Streptomyces rishiriensis MJ773-88K4. II. Structure Determination.

3. Synthesis of the Functionalized Tricyclic Core of Lactonamycin by Oxidative Dearomatization

4. Adducts from quinones and diazoalkanes. Part 10. 2-Diazopropane and 2-methyl-1,4-naphthoquinone; structures and conformations of novel vinylic quinones and epoxides

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