Raghavan, Sadagopan ; Rajender, A. ; Yadav, J. S. (2003) Novel, efficient and stereospecific synthesis of xylo-(2R,3S,4S)-phytosphingosine and threo-(2R,3R)-sphingosine Tetrahedron: Asymmetry, 14 (14). pp. 2093-2099. ISSN 0957-4166
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0957-4166(03)00427-0
Abstract
The stereo- and regioselective elaboration of a bromohydrin from an olefinic precursor and Pummerer ene reaction for carbon---carbon bond formation are the key steps in a novel and flexible synthesis of xylo-phytosphingosine and threo-sphingosine.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 59630 |
Deposited On: | 07 Sep 2011 05:34 |
Last Modified: | 07 Sep 2011 05:34 |
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