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On the formation of 1-O-2′-hydroxyalk-1′-ENYL or 1-O-2′-ketoalkyl glycerophosphatides from 1,2-alkanediol in myelinating brain

✍ Scribed by Toshio Muramatsu; Harald H.O. Schmid


Book ID
115736456
Publisher
Elsevier Science
Year
1972
Tongue
English
Weight
305 KB
Volume
260
Category
Article
ISSN
0005-2760

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Formation, and stereochemistry, of 1,2-O
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In the hydrolysis of O-(2-hydroxypropyl)cellulose, residues of D-gh.ICOSe substituted with a single O-(2-hydroxypropyl) substituent at O-2 (irrespective of the pattern of additional substitution at O-3 or O-6) form 1,2-0-(1-methyl-1,2ethanediyl)-a-D-glucose acetals. Based on the characteristics of 2