Article
Cited 51 time in 
Cited 53 time in 
Cited 53 time in
Metadata Downloads
A short and efficient stereoselective synthesis of all four diastereomers of sphingosine SCIE SCOPUS
- Title
- A short and efficient stereoselective synthesis of all four diastereomers of sphingosine
- Date Issued
- 2002-03-22
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Abstract
- Practical syntheses of all four stereomers of sphingosine from serine have been achieved through highly diastereoselective reduction of the N-trityl protected alpha'-amino enone derivative 5 with NaBH4 and reduction of the free alpha'-amino enone derivative 7 with Zn(BH4)(2). (C) 2002 Elsevier Science Ltd. All rights reserved.
- Keywords
- D-ERYTHRO-SPHINGOSINE; BETA-AMINO ALCOHOLS; L-THREO-SPHINGOSINE; LIPID 2ND-MESSENGERS; EMMONS REACTION; CELL-ADHESION; L-SERINE
- ISSN
- 0957-4166
- Article Type
- Article
- Citation
- TETRAHEDRON-ASYMMETRY, vol. 13, no. 4, page. 343 - 347, 2002-03-22
- Files in This Item:
- There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.