| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5265716 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
An efficient approach for the synthesis of (+) pentenomycin and (â) pentenomycin from d-ribose and d-mannose, respectively, is described using Tebbe olefination of lactones 9 and 7 followed by Me2AlCl induced disfavoured 5-(enol-endo)-exo-trig cyclization.
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Authors
Bejugam Santhosh Kumar, Girija Prasad Mishra, Batchu Venkateswara Rao,