Highly Demanding Cross-Metathesis in the Synthesis of the C16–C30 Fragment of Dolabelide C
Author:
Affiliation:
1. Laboratoire de Synthèse Organique, CNRS UMR 7652, Ecole Polytechnique, DCSO, F-91128 Palaiseau, France
2. WestCHEM, School of Chemistry, University of Glasgow, Joseph Black Building, University Avenue, Glasgow G12 8QQ, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo200466t
Reference33 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. Stereoselective synthesis of C15C24 and C25C30 fragments of dolabelides
4. Ruthenium-SYNPHOS-Catalyzed Asymmetric Hydrogenations: an Entry to Highly Stereoselective Synthesis of the C15−C30 Subunit of Dolabelide A
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