Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1763
Title: Lewis acid-catalyzed stereoselective lactonization and subsequent glycosidation of 2-C-malonyl carbohydrates
Authors: Pimpalpalle, Tukaram M.
VIDADALA, SRINIVASA RAO
HOTHA, SRINIVAS
Linker, Torsten
Dept. of Chemistry
Keywords: Lewis acid-catalyzed
2-C-malonyl carbohydrates
TMSOTf affords allyl, propargyl
Stereoselective cyclization
2011
Issue Date: Aug-2011
Publisher: Royal Society of Chemistry
Citation: Chemical Communications, 47 (37), 10434-10436.
Abstract: Gold(III) bromide is a suitable catalyst for the stereoselective cyclization of 2-C-malonyl carbohydrates to the anomeric center under retention of one ester group. Reopening of the lactones with alcohols in the presence of TMSOTf affords allyl, propargyl and benzyl glycosides with high α-selectivity.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1763
https://doi.org/10.1039/C1CC13425F
ISSN: 1359-7345
1364-548X
Appears in Collections:JOURNAL ARTICLES

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