A Bismuth(III)-Catalyzed Friedel−Crafts Cyclization and Stereocontrolled Organocatalytic Approach to (−)-Platensimycin-Reference-Cited by-同舟云学术

A Bismuth(III)-Catalyzed Friedel−Crafts Cyclization and Stereocontrolled Organocatalytic Approach to (−)-Platensimycin

Published:2010-10-29 Issue:23 Volume:12 Page:5510-5513
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Eey Stanley T.-C.¹,Lear Martin J.¹

Affiliation:

1. Department of Chemistry, Faculty of Science, and Medicinal Chemistry Program of the Life Sciences Institute, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol102390t

Reference65 articles.

1. Platensimycin is a selective FabF inhibitor with potent antibiotic properties

2. Isolation, Structure, and Absolute Stereochemistry of Platensimycin, A Broad Spectrum Antibiotic Discovered Using an Antisense Differential Sensitivity Strategy

3. Platensimycin, a New Antibiotic and “Superbug Challenger” from Nature

4. First racemic total synthesis of (±)-1:

5. Total Synthesis of Platensimycin

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