Synthesis

An efficient stereoselective synthesis of sphingosine

P Kumar, RR Schmidt

Index: Kumar, Pradeep; Schmidt, Richard R. Synthesis, 1998 , # 1 p. 33 - 35

Full Text: HTML

Citation Number: 10

Abstract

This document was downloaded for personal use only. Unauthorized distribution is strictly prohibited. group transformations (Scheme). The choice of introducing a readily removable benzoyl protective group seemed to be more appropriate. Indeed, the hydroxyl group protection of 6 with benzoyl cyanide/triethylamine (£ 7) proceeded smoothly in high yield. Subsequent removal of the isopropylidene group under acid catalysis furnished the diol 8, ...

Related Articles:

Synthesis of D-erythro-sphingosine and D-erythro-ceramide

[Milne, Jacqueline E; Jarowicki, Krzysztof; Kocienski, Philip J; Alonso, Jorge Chemical communications (Cambridge, England), 2002 , # 5 p. 426 - 427]

Synthesis of D-erythro-sphingosine and D-erythro-ceramide

[Milne, Jacqueline E; Jarowicki, Krzysztof; Kocienski, Philip J; Alonso, Jorge Chemical communications (Cambridge, England), 2002 , # 5 p. 426 - 427]

Syntheses of D-erythro-1-deoxydihydroceramide-1-sulfonic acid and phosphonosphingoglycolipid found in marine organisms via a common precursor

[Ohashi, Kinji; Yamagiwa, Yoshiro; Kamikawa, Tadao; Kates, Morris Tetrahedron Letters, 1988 , vol. 29, # 10 p. 1185 - 1188]

Synthesis of D-erythro-sphingosine and D-erythro-ceramide

[Milne, Jacqueline E; Jarowicki, Krzysztof; Kocienski, Philip J; Alonso, Jorge Chemical communications (Cambridge, England), 2002 , # 5 p. 426 - 427]

Synthesis of D-erythro-sphingosine and D-erythro-ceramide

[Milne, Jacqueline E; Jarowicki, Krzysztof; Kocienski, Philip J; Alonso, Jorge Chemical communications (Cambridge, England), 2002 , # 5 p. 426 - 427]

More Articles...