Aravind, Appu ; Baskaran, Sundarababu (2005) 1,3:4,6-Di-O-benzylidene-d-mannitol as a source for novel chiral intermediates through regioselective reductive cleavage Tetrahedron Letters, 46 (5). pp. 743-745. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2004.12.036
Abstract
Synthetically useful chiral intermediates have been synthesized starting from 1,3:4,6-di-O-benzylidene-d-mannitol by regioselective reductive cleavage using BF3·Et2O and Et3SiH in high yields.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Regioselective; Reductive Cleavage; Chiral Intermediates; Chemoselective; Benzylidene Acetals |
| ID Code: | 98549 |
| Deposited On: | 18 Sep 2014 11:11 |
| Last Modified: | 18 Sep 2014 11:11 |
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