An efficient and stereoselective route to 1- deoxy- 5-hydroxy sphingosine analogues
IR@NEIST: CSIR-North East Institute of Science and Technology, Jorhat
View Archive Info| Field | Value | |
| Title |
An efficient and stereoselective route to 1- deoxy- 5-hydroxy sphingosine analogues
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| Creator |
saikia, P P
Goswami, A BAISHYA, G Barua, N C |
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| Subject |
Organic Chemistry
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| Description |
A short and efficient synthesis of 1-deoxy-5-hydroxy sphingolipid is described. The key steps involved are
a Jacobsen hydrolytic kinetic resolution (HKR) and Shibasaki 19s asymmetric Henry reaction
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| Publisher |
Elsevier
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| Date |
2009
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| Type |
Article
PeerReviewed |
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| Format |
application/pdf
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| Identifier |
http://neist.csircentral.net/63/1/2674_TL_50(12)2009_p1328%2D30.pdf
saikia, P P and Goswami, A and BAISHYA, G and Barua, N C (2009) An efficient and stereoselective route to 1- deoxy- 5-hydroxy sphingosine analogues. Tetrahedron Letters, 50 (12). pp. 1328-1330. |
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| Relation |
http://neist.csircentral.net/63/
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