Sen'i Gakkaishi
Online ISSN : 1884-2259
Print ISSN : 0037-9875
SYNTHESES OF MONO- AND DI-AMINATED STARCHES
Takuma TeshirogiHideo YamamotoMunenori SakamotoHiroaki Tonami
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1979 Volume 35 Issue 11 Pages T479-T485

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Abstract
Monoaminodeoxystarch (6) having 0.92 as the degree of substitution by amino group was prepared by p-toluenesulfonylation of soluble starch, followed by the reaction with sodium azide, O-aceylation to impart solubility, and the reduction with lithium aluminum hydride. 6-Amino-6-deoxy-D-glucose was found as a main product in the hydrolyzate of 6. Diaminated starch (12) having 1.60 as the degree of substitution by amino group was prepared by p-toluenesulfonylation, followed by the reaction with sodium azide, and the reduction with lithium aluminum hydride.
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© The Society of Fiber Science and Technology, Japan
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