STEREOSELECTIVE SYNTHESIS OF 2-O-BENZYL-1-O-HEXADECYL-SN-GLYCEROL

BAUER, F and RUESS, KP and LIEFLANDER, M (1992) STEREOSELECTIVE SYNTHESIS OF 2-O-BENZYL-1-O-HEXADECYL-SN-GLYCEROL. LIEBIGS ANNALEN DER CHEMIE (1). pp. 47-50. ISSN 0170-2041,

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Abstract

Due to the versatility of 2-O-benzyl-1-O-hexadecyl-sn-glycerol (7) as building block for various alkyl ether lipids and alkyl ether lyso-lipids, 7 was prepared from D-mannit following two different strategies. The final product 7 was obtained either via the intermediate 1,2-O-isopropylidene-sn-glycerol (1) or via 3,4-O-isopropylidene-D-mannit (8) in an overall yield of 6% or 11%, respectively.

Item Type: Article
Uncontrolled Keywords: PLATELET ACTIVATING FACTOR; ANALOGS; LYSOGLYCOLIPIDS, GLYCERYL ETHERS; GLYCEROL, 2-O-BENZYL-1-O-HEXADECYL; CARBOHYDRATES
Depositing User: Dr. Gernot Deinzer
Last Modified: 19 Oct 2022 08:44
URI: https://pred.uni-regensburg.de/id/eprint/54714

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