An “Aprotic” Tamao Oxidation/Syn-Selective Tautomerization Reaction for the Efficient Synthesis of the C(1)–C(9) Fragment of Fludelone
Author:
Affiliation:
1. Department of Chemistry, Columbia University, New York, New York 10027, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol302221s
Reference24 articles.
1. The Chemistry and Biology of Epothilones—The Wheel Keeps Turning
2. bAltmann, K.H.; Höfle, G.; Müller, R.; Mulzer, J.; Prantz, K.InProgress in the Chemistry of Organic Natural Products, Vol. 90: The Epothilones: An Outstanding Family of Anti-Tumor Agents. From Soil to the Clinic;Kinghorn, A. D.; Falk, H.; Kobayashi, J., Eds.Springer:Vienna, 2009; p260.
3. Recent Developments in the Syntheses of the Epothilones and Related Analogues
4. Discovery of (E)-9,10-Dehydroepothilones through Chemical Synthesis: On the Emergence of 26-Trifluoro-(E)-9,10-dehydro-12,13-desoxyepothilone B as a Promising Anticancer Drug Candidate
5. On the Remarkable Antitumor Properties of Fludelone: How We Got There
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