Facile Synthesis of β- and α-Arabinofuranosides and Application to Cell Wall Motifs of M. tuberculosis

dc.contributor.author	THADKE, SHIVAJI A.	en_US
dc.contributor.author	Mishra, Bijoyananda	en_US
dc.contributor.author	HOTHA, SRINIVAS	en_US
dc.date.accessioned	2019-02-14T05:00:10Z
dc.date.available	2019-02-14T05:00:10Z
dc.date.issued	2013-05	en_US
dc.identifier.citation	Organic Letters, 15(10), 2466-2469.	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.issn	1523-7052	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1597
dc.identifier.uri	https://doi.org/10.1021/ol400931p	en_US
dc.description.abstract	Propargyl 1,2-orthoesters of arabinose are exploited for the synthesis of 1,2-trans furanosides; easily accessible 1,2-trans ribofuranosides are converted to challenging 1,2-cis-arabinofuranosides by oxidoreduction. Utility of these protocols was demonstrated by the successful synthesis of major structural motifs present in the cell surface of Mycobacterium tuberculosis. Key furanosylations were carried out under gold-catalyzed glycosidation conditions.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Facile Synthesis	en_US
dc.subject	-- and --Arabinofuranosides	en_US
dc.subject	Cell Wall Motifs	en_US
dc.subject	M. tuberculosis	en_US
dc.subject	Tuberculosis	en_US
dc.subject	2013	en_US
dc.title	Facile Synthesis of β- and α-Arabinofuranosides and Application to Cell Wall Motifs of M. tuberculosis	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Organic Letters	en_US
dc.publication.originofpublisher	Foreign	en_US