Journal article
Cerebroside analogues from 3-phenylserines
Chemistry and physics of lipids, v 19(4), pp 347-355
Aug 1977
PMID: 908106
Abstract
Cerebroside analogues were synthesized from DL-
threo-and DL-
erythro-3-phenylserines by the following sequence of reactions: estirification, N-acylation, reduction with sodium bis (2-methoxyethoxy)-aluminum hydride (SMEAH), and condensation with acetobromoglucose followed by deacetylation. Mass spectrometry disclosed that the glycosidic bond was formed at the primary hydroxyl group.
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Details
- Title
- Cerebroside analogues from 3-phenylserines
- Creators
- Benjamin Weiss - Columbia University
- Publication Details
- Chemistry and physics of lipids, v 19(4), pp 347-355
- Publisher
- Elsevier Ireland Ltd
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Pharmacology and Physiology
- Web of Science ID
- WOS:A1977DW91600007
- Scopus ID
- 2-s2.0-0017521344
- Other Identifier
- 991020836600204721