Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2155
Title: Propargyl 1,2-Orthoesters for a Catalytic and Stereoselective Synthesis of Pyrimidine Nucleosides
Authors: Rao, Boddu Venkateswara
Manmode, Sujit
HOTHA, SRINIVAS
Dept. of Chemistry
Keywords: Catalytic and Stereoselective
Catalytic and Stereoselective
High-yielding protocol
2015
Issue Date: Feb-2015
Publisher: American Chemical Society
Citation: Journal of Organic Chemistry, 80 (3),1499-1505.
Abstract: Pyrimidine nucleosides are synthesized by using propargyl 1,2-orthoesters and Au(III) salt as a catalyst. Strategically positioned 1,2-orthoesters are found to yield only 1,2-trans nucleosides and enable preparation of 2′-OH containing pyrimidine nucleosides. The glycosyl donor employed in this study is stable and easily accessible. The identified high-yielding protocol is mild, diastereoselective, and catalytic.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2155
https://doi.org/10.1021/jo502413z
ISSN: 1499-1505
1520-6904
Appears in Collections:JOURNAL ARTICLES

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