Total Synthesis of the Potent HIF-1 Inhibitory Antitumor Natural Product, (8R)-Mycothiazole, via Baldwin–Lee CsF/CuI sp3–sp2-Stille Cross-Coupling. Confirmation of the Crews Reassignment
Author:
Affiliation:
1. The School of Chemistry & Chemical Engineering and the Centre for Cancer Research and Cell Biology (CCRCB), the Queen’s University Belfast, Stranmillis Road, Belfast BT9 5AG, Northern Ireland, United Kingdom
Funder
Queen's University Belfast
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b01966
Reference21 articles.
1. Mycothiazole, a polyketide heterocycle from a marine sponge
2. A Reassignment of (−)-Mycothiazole and the Isolation of a Related Diol
3. Asymmetric Total Synthesis of (−)-Mycothiazole
4. Total synthesis of mycothiazole, a polyketide heterocycle from marine sponges
5. Total Synthesis of (±)-Mycothiazole and Formal Enantioselective Approach
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