Total Syntheses of (R)-Strongylodiols C and D.
J Nat Prod
; 79(1): 244-7, 2016 Jan 22.
Article
em En
| MEDLINE
| ID: mdl-26735019
ABSTRACT
The first total syntheses of two marine natural products, (R)-strongylodiols C and D, with 99% ee were achieved. The key steps of the strategy include the zipper reaction of an alkyne, the asymmetric alkynylation of an unsaturated aliphatic aldehyde catalyzed with Trost's ProPhenol ligand, and the Cadiot-Chodkiewicz cross-coupling reaction of a chiral propargylic alcohol with a bromoalkyne.
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MEDLINE
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Produtos Biológicos
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Álcoois
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Alcinos
Idioma:
En
Ano de publicação:
2016
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Article