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 |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.