Synthesis of the Sulfonate Analogue of Seminolipid via Horner-Wadsworth-Emmons Olefination

L FRANCHINI; F COMPOSTELLA; D COLOMBO; Luigi PANZA; F. RONCHETTI

Synthesis of the Sulfonate Analogue of Seminolipid via Horner-Wadsworth-Emmons Olefination

L FRANCHINI
, F COMPOSTELLA
, D COLOMBO
, Luigi PANZA
, F. RONCHETTI

Dipartimento di Scienze del Farmaco

Risultato della ricerca: Contributo su rivista › Articolo in rivista

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
pagine (da-a)	5363-5366
Numero di pagine	4
Rivista	Journal of Organic Chemistry
Volume	75
Stato di pubblicazione	Pubblicato - 2010

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http://hdl.handle.net/11579/24265

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title = "Synthesis of the Sulfonate Analogue of Seminolipid via Horner-Wadsworth-Emmons Olefination",

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.",

author = "L FRANCHINI and F COMPOSTELLA and D COLOMBO and Luigi PANZA and F. RONCHETTI",

year = "2010",

language = "English",

volume = "75",

pages = "5363--5366",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

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TY - JOUR

T1 - Synthesis of the Sulfonate Analogue of Seminolipid via Horner-Wadsworth-Emmons Olefination

AU - FRANCHINI, L

AU - COMPOSTELLA, F

AU - COLOMBO, D

AU - PANZA, Luigi

AU - RONCHETTI, F.

PY - 2010

Y1 - 2010

N2 - (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.

AB - (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.

UR - https://iris.uniupo.it/handle/11579/24265

M3 - Article

SN - 0022-3263

VL - 75

SP - 5363

EP - 5366

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

ER -

Synthesis of the Sulfonate Analogue of Seminolipid via Horner-Wadsworth-Emmons Olefination

Abstract

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