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Enantioselective Approach to Polyhydroxylated Compounds Using Chiral Sulfoxides: Synthesis of Enantiomerically Pure myo-Inositol and Pyrrolidine Derivatives
A short enantioselective synthesis of the biologically important myo-inositol derivative I and the pyrrolidine derivative II is described. The molecule 3, a diketo disulfoxide readily made from tartaric acid, is the key intermediate. The sulfinyl group controlled completely the very high stereoselec...
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Published in: | Journal of organic chemistry 1998-11, Vol.63 (24), p.8918-8921 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A short enantioselective synthesis of the biologically important myo-inositol derivative I and the pyrrolidine derivative II is described. The molecule 3, a diketo disulfoxide readily made from tartaric acid, is the key intermediate. The sulfinyl group controlled completely the very high stereoselection observed. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/jo9811569 |