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Stereocontrolled total synthesis of leukotriene B4

Authors :
Avignon-Tropis, M.
Berjeaud, J.M.
Pougny, J.R.
Frechard-Ortuno, I.
Guillerm, D.
Linstrumelle, G.
Source :
Journal of Organic Chemistry. Jan 17, 1992, Vol. 57 Issue 2, p651, 4 p.
Publication Year :
1992

Abstract

The reduction of D-mannitol and 2-deoxy-D-ribose with (E)-dichloroethylene resulted in the stereocontrolled synthesis of leukotriene B. The process involved palladium-copper catalysts to provide sequential substitution of dichloroethylenes E and Z. The selective reduction, prior to the coupling of the chiral building blocks, also produced other stereoisomers of leukotriene B aside from the desired chiral structures.

Details

ISSN :
00223263
Volume :
57
Issue :
2
Database :
Gale General OneFile
Journal :
Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
edsgcl.12924543