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Synthesis of three isomers of linoleic acid

Thesis (Ph.D.)--Boston University / Three skipped unsaturated fatty acids, 8,11-octadecadienoic acid, 10,13-octadecadienoic acid and 11,14-octadecadienoic acid have been synthesized via skipped acetylenic intermediates.
Coupling an w-chloroacetylenic Grignard derivative I with a propargylic bromide II in tetrahydrofuran in the presence of cuprous chloride catalyst yielded a 1-chloroheptadecadiyne III, which was reduced stereospecifically and selectively to the di-cis-1-chloroheptadecadiene IV by two treatments with diisobutylaluminum hydride. The diene IV was converted to the Grignard reagent which upon carbonation and acidification gave the octadecadienoic acid V[TRUNCATED]

Identiferoai:union.ndltd.org:bu.edu/oai:open.bu.edu:2144/31348
Date January 1961
CreatorsBruno, John Joseph
PublisherBoston University
Source SetsBoston University
Languageen_US
Detected LanguageEnglish
TypeThesis/Dissertation
RightsBased on investigation of the BU Libraries' staff, this work is free of known copyright restrictions.

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