Ruthenium-SYNPHOS-Catalyzed Asymmetric Hydrogenations: an Entry to Highly Stereoselective Synthesis of the C15−C30 Subunit of Dolabelide A
Author:
Affiliation:
1. Laboratoire de Synthèse Sélective Organique et Produits Naturels UMR 7573 CNRS, ENSCP, 11 rue Pierre et Marie Curie, 75231 Paris Cedex 01, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol801493w
Reference40 articles.
1. Dolabelides A and B, cytotoxic 22-membered macrolides isolated from the sea hare Dolabella auricularia
2. Dolabelides C and D, Cytotoxic Macrolides Isolated from the Sea Hare Dolabella auricularia
3. Diastereoselective Synthesis of Protected syn 1,3-Diols: Preparation of the C16−C24 Portion of Dolabelides
4. Approach to the Synthesis of Dolabelides A and B: Fragment Synthesis by Tandem Silylformylation−Crotylsilylation
5. Stereoselective synthesis of the C1–C13 segment of dolabelide B
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