Synthesis of l-lyxo-phytosphingosine and its 1-phosphonate analogue using a threitol acetal synthon.
Xuequan Lu, Hoe-Sup Byun, Robert Bittman
Index: J. Org. Chem. 69(16) , 5433-8, (2004)
Full Text: HTML
Abstract
The first synthesis of an isosteric phosphonate analogue of the aminotriol lipid phytosphingosine (3), together with an improved synthesis of (2S,3S,4S)-phytosphingosine (2), are described. A key intermediate is 3-pentylidene acetal 9, which was prepared in two steps from dimethyl 2,3-O-benzylidene-d-tartrate (7).Copyright 2004 American Chemical Society
Related Compounds
Related Articles:
2004-04-01
[Am. J. Hum. Genet. 74(4) , 745-51, (2004)]
2005-01-19
[J. Am. Chem. Soc. 127(2) , 506-7, (2005)]
1994-06-01
[Exp. Eye Res. 58(6) , 665-74, (1994)]
2000-11-03
[Carbohydr. Res. 329(2) , 409-22, (2000)]
1992-01-01
[Caries Res. 26(2) , 84-8, (1992)]