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Cerebroside analogues from 3-phenylserines
Chemistry and Physics of Lipids, 1977Cerebroside analogues were synthesized from DL-threo-and DL-erythro-3-phenylserines by the following sequence of reactions: esterification, N-acylation, reduction with sodium bis (2-methoxyethoxy)-aluminum hydride (SMEAH), and condensation with acetobromoglucose followed by deacetylation.
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1914
Mit Hilfe des Baryt-Acetonverfahrens nach Loening -Thierfelder1) lassen sieh aus Protagon 33–39% Cerebroside (berechnet der angewandten Protagonmenge) erhalten2)
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Mit Hilfe des Baryt-Acetonverfahrens nach Loening -Thierfelder1) lassen sieh aus Protagon 33–39% Cerebroside (berechnet der angewandten Protagonmenge) erhalten2)
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1983
Ceramide* is the basic component of sphingolipids and a key intermediate of both synthesis and degradation of all sphingolipids.1 Major brain sphingolipids are cerebrosides, sulfatides, sphingomyelins, and gangliosides. These are unique to and abundant in the nervous system. In addition, there is a small quantity of free ceramide in brain.
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Ceramide* is the basic component of sphingolipids and a key intermediate of both synthesis and degradation of all sphingolipids.1 Major brain sphingolipids are cerebrosides, sulfatides, sphingomyelins, and gangliosides. These are unique to and abundant in the nervous system. In addition, there is a small quantity of free ceramide in brain.
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Chemistry of Phosphatides and Cerebrosides
Physiological Reviews, 1952W D, CELMER, H E, CARTER
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