Premium
Hydrogenation of unsaturated fatty acid methyl esters with diimide from hydroxylamine‐ethyl acetate
Author(s) -
Gangadhar A.,
Chandrasekhara Rao T.,
Subbarao R.,
Lakshminarayana G.
Publication year - 1989
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/bf02661982
Subject(s) - hydroxylamine , chemistry , organic chemistry , methyl oleate , diimide , fatty acid , double bond , reagent , hydrazide , linoleic acid , hydrazine (antidepressant) , castor oil , ethyl ester , oleic acid , catalysis , biochemistry , molecule , perylene
Methyl esters of 10‐undecenoic, oleic, linoleic and castor oil fatty acids were hydrogenated with hydroxylamine‐ethyl acetate reagent under nitrogen, without change in position and configuration of double bonds. The fatty acid ester was also found to participate in the generation of diimide. No hydrazide was formed.