Synthesis of beta-C-Galactosyl ceramide and its new aza variant via the Horner-Wadsworth-Emmons reaction

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DC Field	Value	Language
dc.contributor.author	Gorantla, J N	-
dc.contributor.author	Ravi S Lankalapalli	-
dc.date.accessioned	2014-08-08T04:53:16Z	-
dc.date.available	2014-08-08T04:53:16Z	-
dc.date.issued	2014	-
dc.identifier.citation	Journal of Organic Chemistry 79(11):5193-5200;6 Jun 2014	en_US
dc.identifier.issn	0022-3263	-
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1604	-
dc.description.abstract	A simple strategy for the synthesis of beta-C-galactosyl ceramide and its new aza-variant analogue is described using the Horner-Wadsworth-Emmons reaction as the key step in combining the sugar and aglycone portions.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	beta-C-Galactosyl Ceramide	en_US
dc.subject	Horner-Wadsworth-Emmons reaction	en_US
dc.subject	Aza-variant analogue	en_US
dc.title	Synthesis of beta-C-Galactosyl ceramide and its new aza variant via the Horner-Wadsworth-Emmons reaction	en_US
dc.type	Article	en_US
Appears in Collections:	2014

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