Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5277897 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Introduction of an allyl functionality at C-3 of 1,2:5,6-di-O-isopropylidene-α-d-glucofuranose followed by olefination at C-5 and C-6 provided 1,6-diene 5 which, upon ring closing metathesis and subsequent functional group manipulation, furnished the key cyclopentene diacetate 7, which was elaborated to carbanucleoside (â)-carbovir 1.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Biswajit G. Roy, Prithwish K. Jana, Basudeb Achari, Sukhendu B. Mandal,