Abstract
(Figure presented) The first synthesis of the sulfonate analogue of seminolipid, the main sulfoglycolipid in mammalian sperm, is reported. Installation of the sulfonate unit was accomplished by a quite unexplored strategy based on Horner-Wadsworth-Emmons olefination on a 3 ′-keto-galactoside, followed by stereoselective double bond reduction.
Lingua originale | Inglese |
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pagine (da-a) | 5363-5366 |
Numero di pagine | 4 |
Rivista | Journal of Organic Chemistry |
Volume | 75 |
Numero di pubblicazione | 15 |
DOI | |
Stato di pubblicazione | Pubblicato - 6 ago 2010 |