| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222402 | Tetrahedron | 2011 | 5 Pages |
Abstract
An efficient method for the stereoselective synthesis of l-ribose was accomplished starting from commercially inexpensive d-fructose. The intermediates in the process can serve as versatile precursors for the preparation of l-nucleoside analogues.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ramu Sridhar Perali, Suresh Mandava, Ramakrishna Bandi,