Characterization and synthesis of mono- and diphytanyl ethers of glycerol.

Abstract:

:The methanolyzed lipids of the extreme halophile, Halobacterium cutirubrum, were separated into glycerol diether and glycerol monoether fractions. The diether was shown by synthesis to be 2,3-di-O-(3'R,7'R,11'R,15'-tetramethylhexadecyl)-sn-glycerol. The monoether fraction was separated by thin-layer chromatography on boric acid-impregnated silicic acid into about equal amounts of alpha- and -isomers. The alpha-isomer was found to be identical with the synthetic 3-O-(3'R,7'R,11'R,15'-tetramethylhexadecyl)-sn-glycerol, and the -isomer was identical with the synthetic 2-O-(3'R,7'R,11'R,15'-tetramethylhexadecyl) glycerol.

journal_name

J Lipid Res

authors

Joo CN,Shier T,Kates M

subject

Has Abstract

pub_date

1968-11-01 00:00:00

pages

782-8

issue

6

eissn

0022-2275

issn

1539-7262

journal_volume

9

pub_type

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