Tandem Conjugate Addition−Elimination for the Diastereoselective Synthesis of 4E-Alkenyl syn-1,3-Diols
Author:
Affiliation:
1. Laboratoire de Synthèse Organique, UMR CNRS 7652, Ecole Polytechnique, DCSO, F-91128 Palaiseau, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol701624y
Reference13 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. Stereoselective synthesis of the C1–C13 segment of dolabelide B
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