Enantioselective total synthesis of (2S,3R,4R)-D-xylo-phytosphingosine from substituted azetidin-2-one
| Title | Enantioselective total synthesis of (2S,3R,4R)-D-xylo-phytosphingosine from substituted azetidin-2-one |
| Publication Type | Journal Article |
| Year of Publication | 2009 |
| Authors | Pandey, G, Tiwari, DKumar |
| Journal | Tetrahedron Letters |
| Volume | 50 |
| Issue | 26 |
| Pagination | 3296-3298 |
| Date Published | JUL |
| ISSN | 0040-4039 |
| Keywords | beta-lactam, Enantioselective synthesis, Sphingosine, Wittig reaction |
| Abstract | Enantiomerically pure (2S,3R,4R)-D-xylo phytosphingosine is synthesized in 36% overall yield in seven steps from known beta-lactam (8) derived from D-mannitol triacetonide. (C) 2009 Elsevier Ltd. All rights reserved. |
| DOI | 10.1016/j.tetlet.2009.02.050 |
| Type of Journal (Indian or Foreign) | Foreign |
| Impact Factor (IF) | 2.618 |
Divison category:
Organic Chemistry