Total Synthesis of (−)-Apicularen A
Author:
Affiliation:
1. Contribution from the Department of Chemistry and Center for Chemical Methodology and Library Design, Metcalf Center for Science and Engineering, 590 Commonwealth Avenue, Boston University, Boston, Massachusetts 02215
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja037957x
Reference30 articles.
1. Apicularens A and B, New Cytostatic Macrolides from Chondromyces Species (Myxobacteria): Production, Physico-chemical and Biological Properties.
2. Apicularen A and B, Cytotoxic 10-Membered Lactones with a Novel Mechanism of Action fromChondromyces Species (Myxobacteria): Isolation, Structure Elucidation, and Biosynthesis
3. Total synthesis and biological evaluation of apicularen A and synthetic analogs
4. Enantioselective total synthesis of salicylihalamides A and B
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