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Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides
Author(s) -
Avidon Victor,
Shani Ar
Publication year - 1994
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/bf02542267
Subject(s) - double bond , chemistry , epoxide , surface modification , molecule , ring (chemistry) , bromine , organic chemistry , polymer chemistry , catalysis
The apolar and hydrophobic jojoba molecule was made more hydrophilic by the incorporation of primary amino groups via the introduction and subsequent reduction of azido groups. The azides were obtained by the substitution of bromine or a mesylate group introduced into the jojoba oil molecule; by opening of the epoxide ring in epoxy jojoba; or by the addition of bromoazide to the double bonds of jojoba.