Stereoselective synthesis of the C1–C13 segment of dolabelide B
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Dolabelides A and B, cytotoxic 22-membered macrolides isolated from the sea hare Dolabella auricularia
2. Diastereoselective Synthesis of Protected syn 1,3-Diols: Preparation of the C16−C24 Portion of Dolabelides
3. Stereoselective synthesis of C15C24 and C25C30 fragments of dolabelides
4. Approach to the Synthesis of Dolabelides A and B: Fragment Synthesis by Tandem Silylformylation−Crotylsilylation
5. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
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