## Abstract A stereospecific gas chromatography (GC) method using a (6‐__O__‐__t__ butyldimethylsilyl‐2,3‐di‐__O__‐methyl)‐β‐cyclodextrin as the chiral stationary phase has been developed and validated for the determination of the enantiomers of 1,2‐__O__‐isopropylidene‐sn‐glycerol (IPG), an import
An improved method for the preparation of 1,2-isopropylidene-SN-glycerol
✍ Scribed by Hansjörg Eibl
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 258 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0009-3084
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✦ Synopsis
A simple and fast route for the preparation of 1,2-isopropylidene-sn-glycerol from Dmannitol in 45% yield is described. The value of optical rotation, [a] ~ + 15.2 °, is higher than usual indicating considerable racemization for other procedures, Since 1,2-isopropylidene-sn-glycerol serves as general intermediate for the synthesis of glycerides and of phosphoglycerides these lipids contain substantial amounts of the isomer, for instance 1,2-dipalmitoyl-sn-glycerol-3-phosphocholine may consist of up to 15% of 2,3-dipalmitoyl-sn-glycerol-1-phosphocholine in earlier preparations,
📜 SIMILAR VOLUMES
In this and a following paper we describe two complementary strategies for the synthesis of uniform or mixed glyceryl esters and ethers. Using these, virtually any compound of the form l-X-2-Y-3-Z-sn-glycerol can be synthesized, where X, Y and Z are acyl or alkyl groups or may be absent. Yields are
## B i o l o g i c a l l y l a b e l l e d [l-14C) g l y c e r o l ( L -[ l -' " C ) g l y c e r o l ) 048 prepared by a two s t e p p r o c e s s . S t e p one i n v o 1 v e d t h e p r e p a r a t i o n of [I -C ] g 2 y ce r o 1 3 -p ho sp ha t e from l4C02 and D-ribuloee 1,5 -diphoephate u s i
## Abstract 2‐__O__‐Arachidonoyl‐1‐__O__‐stearoyl‐__sn__‐glycerol is the most abundant molecular species of the 1,2‐diacyl‐__sn__‐glycerol signaling lipids in neural tissue. The facile preparation of 2‐__O__‐[1′‐^14^C]arachidonoyl‐1‐__O__‐stearoyl‐__sn__‐glycerol from 2‐__O__‐[1′‐^14^C]arachidonoyl