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SnCl4 Promoted Efficient Cleavage of Acetal/Ketal Groups with the Assistance of Water in CH2Cl2.


ABSTRACT: Acetalization and deacetalation are a pair of routine manipulations to protect and deprotect the 4- and 6-hydroxyl groups of glycosides in the synthesis of glycosyl building blocks. In this study, we found that treatment of SnCl4 with various carbohydrates containing acetal/ketal groups with the assistance of water in CH2Cl2 led to deacetalization/deketalization products in almost quantitative yields. In addition, for substrates containing both acetal/ketal and p-methoxylbenzyl groups, we also found that the p-methoxylbenzyl group was selectively cleaved by the use of a catalytic amount of SnCl4, while the acetal/ketal groups remained. Furthermore, based on this, 4,6-benzylidene glycosides can be conveniently converted to 4,6-OAc or 4-OH, 6-OAc glycosides.

SUBMITTER: Luo T 

PROVIDER: S-EPMC9736348 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature

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SnCl<sub>4</sub> Promoted Efficient Cleavage of Acetal/Ketal Groups with the Assistance of Water in CH<sub>2</sub>Cl<sub>2</sub>.

Luo Tao T   Xu Tian-Tian TT   Guo Yang-Fan YF   Dong Hai H  

Molecules (Basel, Switzerland) 20221126 23


Acetalization and deacetalation are a pair of routine manipulations to protect and deprotect the 4- and 6-hydroxyl groups of glycosides in the synthesis of glycosyl building blocks. In this study, we found that treatment of SnCl<sub>4</sub> with various carbohydrates containing acetal/ketal groups with the assistance of water in CH<sub>2</sub>Cl<sub>2</sub> led to deacetalization/deketalization products in almost quantitative yields. In addition, for substrates containing both acetal/ketal and <  ...[more]

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