TY - JOUR
T1 - Diacetylenic sterols
T2 - New potentially photopolymerizable lipids
AU - Vilchèze, Catherine
AU - Bittman, Robert
PY - 1995
Y1 - 1995
N2 - Cholesterol analogues with a diacetylenic moiety in their side chains have been prepared from bisnorcholenic acid, using 1,4-bis(trimethylsilyl)buta-1,3- diyne as the synthon to introduce the polymerizable group. A preliminary study of their potential as polymerizable sterols has been carried out by exposing aqueous dispersions (with or without phospholipids) to UV light at 5 °C.
AB - Cholesterol analogues with a diacetylenic moiety in their side chains have been prepared from bisnorcholenic acid, using 1,4-bis(trimethylsilyl)buta-1,3- diyne as the synthon to introduce the polymerizable group. A preliminary study of their potential as polymerizable sterols has been carried out by exposing aqueous dispersions (with or without phospholipids) to UV light at 5 °C.
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U2 - 10.1039/p19950002937
DO - 10.1039/p19950002937
M3 - Article
AN - SCOPUS:0000766402
SN - 0260-1826
VL - 91
SP - 2937
EP - 2940
JO - Journal of the Chemical Society, Perkin Transactions 1
JF - Journal of the Chemical Society, Perkin Transactions 1
IS - 22
ER -