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• W1992472205 abstract "Two kinds of amphoteric glycosphingolipid analogues from the earthworm Pheretima hilgendorfi were synthesized as follows: The key reaction is a coupling of a phosphocholine group at the position C-6 of 1 and 6 which was attempted using 2-chloro-2-oxo-1,3,2-dioxaphospholane, followed by reaction of the resulting cyclic phosphate intermediate with anhydrous trimethylamine to give 2 and 7. Subsequent debenzylation afforded target compounds (3,8). Their ability to inhibit the histamine release in vitro was examined." @default.
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• W1992472205 date "2001-01-01" @default.
• W1992472205 modified "2023-10-11" @default.
• W1992472205 title "Synthetic Studies on Glycosphingolipids from Protostomia Phyla: Synthesis of Amphoteric Glycolipid Analogues Containing a Phosphocholine Residue from the Earthworm Pheretima hilgendorfi." @default.
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• W1992472205 doi "https://doi.org/10.1248/cpb.49.1464" @default.
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