Bulletin de la Société chimique de France

Studies related to fatty acid desaturation. I, Preparation of methyl-substituted nonanols, nonyl bromides and total synthesis of new branched oleic acids

S Genard, H Patin

Index: Genard, S.; Patin, H. Bulletin de la Societe Chimique de France, 1991 , # 3 p. 397 - 406

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Citation Number: 16

Abstract

Résumé/Abstract Convenient pathways for the synthesis of seven structurally defined isomers of methyl-nonanols and methyl-nonylbromides are described. These synthons are used to perform Wittig reactions between convenient phosphoranes and aldehydes in order to obtain seven new octadecenoic acids bearing a methyl grouping on carbons 11 to 17

 Related Synthetic Route

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