Diacetylenic sterols: New potentially photopolymerizable lipids

Catherine Vilchèze, Robert Bittman

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

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.

Original languageEnglish (US)
Pages (from-to)2937-2940
Number of pages4
JournalJournal of the Chemical Society, Perkin Transactions 1
Volume91
Issue number22
StatePublished - Dec 1 1995
Externally publishedYes

Fingerprint

Sterols
Dispersions
Ultraviolet radiation
Phospholipids
Cholesterol
Lipids
Acids

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Diacetylenic sterols : New potentially photopolymerizable lipids. / Vilchèze, Catherine; Bittman, Robert.

In: Journal of the Chemical Society, Perkin Transactions 1, Vol. 91, No. 22, 01.12.1995, p. 2937-2940.

Research output: Contribution to journalArticle

@article{d25328fdcdcf45eba4a539d83298ca80,
title = "Diacetylenic sterols: New potentially photopolymerizable lipids",
abstract = "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.",
author = "Catherine Vilch{\`e}ze and Robert Bittman",
year = "1995",
month = "12",
day = "1",
language = "English (US)",
volume = "91",
pages = "2937--2940",
journal = "Journal of the Chemical Society, Perkin Transactions 1",
issn = "1472-7781",
publisher = "Chemical Society",
number = "22",

}

TY - JOUR

T1 - Diacetylenic sterols

T2 - New potentially photopolymerizable lipids

AU - Vilchèze, Catherine

AU - Bittman, Robert

PY - 1995/12/1

Y1 - 1995/12/1

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.

UR - http://www.scopus.com/inward/record.url?scp=0000766402&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0000766402&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0000766402

VL - 91

SP - 2937

EP - 2940

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

SN - 1472-7781

IS - 22

ER -