Chem. J. Chinese Universities ›› 1992, Vol. 13 ›› Issue (9): 1212.
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WU Hong-Qiao, LI Cui-Juan, WANG Shi-Yu
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Abstract: Reaction of sucrose with trialkyl orthoacetate,subsequent tritylation,acetylation,and detritylation afforded derivatives of sucrose acetate by selectively blocking specific hydroxyls in sucrose and 4-6 acetyl migration.The treatment of sucrose alkyl 4,6-orthoacetate hexaaeetate with water or alcohol in the presence of an acid catalyst afforded corresponding 2,3,6,1',3',4',6'-hepta-O-acetylsucrose and 2,3.1',3',4',6'-hexa-O-acetylsucrose.These derivatives of sucrose acetate were available from sucrochemical studies and have been developed as convenient intermediate for the synthesis of sucrose derivatives.
Key words: Sucrose acetate, Trialkyl orthoacetate, Sucrose aikyl 4,6-orthoacetate hexaacetate
TrendMD:
WU Hong-Qiao, LI Cui-Juan, WANG Shi-Yu . Studies on the Selectively Protecting Groups of Hydroxyls in Sucrose[J]. Chem. J. Chinese Universities, 1992, 13(9): 1212.
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http://www.cjcu.jlu.edu.cn/EN/Y1992/V13/I9/1212