STUDY ON THE SYNTHESIS, RING-OPENING REACTION AND GLYCOSIDATION OF 1,6-ANHYDRO-2,4-DI-O-BENZYL-β-D-GLUCOPYRANOSE  

STUDY ON THE SYNTHESIS, RING-OPENING REACTION AND GLYCOSIDATIONOF 1,6-ANHYDRO-2,4-DI-O-BENZYL-β-D-GLUCOPYRANOSE

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作  者:Hong LIANG Chang Pei FEI(Institute of Chemistry. Academia Sinica. Beijing 100080) 

出  处:《Chinese Chemical Letters》1994年第8期655-658,共4页中国化学快报(英文版)

摘  要:A series of compounds had been synthesised from 1.6-anhydro-2,4-di-O-benzyl-β-D-glucopyranose with good yields.The The effects of C-3 protecting groups on ring-opening reaction and the glycosidation of α-D-glucopyranosyl bromides were studied.A series of compounds had been synthesised from 1.6-anhydro-2,4-di-O-benzyl-β-D-glucopyranose with good yields.The The effects of C-3 protecting groups on ring-opening reaction and the glycosidation of α-D-glucopyranosyl bromides were studied.

关 键 词:DI BENZYL ANHYDRO AND 

分 类 号:O621.25[理学—有机化学]

 

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