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The carbonyl group plays a predominant role in organic synthesis due to its electrophilic nature. One of the major com-mon problems during many multi-step syntheses in organic, medicinal, carbohydrate and drug design chemistry is how to protect the carbonyl group from nucleophilic attack until its electrophilic properties could be utilized. Therefore, the pro-tection and deprotcetion of carbonyl groups remain an area of interest in synthetic organic chemistry. Among the carbonyl protecting groups, 1,3-oxathiolanes are important class of com-pounds that are more stable than corresponding O,O-acetals under acidic conditions and compared with S,S-acetals are more easily deprotected.

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An Efficient and Chemoselective Method for Synthesis of 1,3-Oxathiolanes from Aldehydes and their Deprotection Catalyzed by V(HSO<sub>4</sub>)<sub>3</sub>

An Efficient and Chemoselective Method for Synthesis of 1,3-Oxathiolanes from Aldehydes and their Deprotection Catalyzed by V(HSO4)3

An Efficient and Chemoselective Method for Synthesis of 1,3-Oxathiolanes from Aldehydes and their Deprotection Catalyzed by V(HSO₄)₃