Enzymatic Deprotection of Methylthiomethyl Esters: Synthesis of O-(Carbamoyl) and O-(Sulfamoyl)salicylic Acids: Synthetic Communications: Vol 21, No 10-11

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 21, 1991 - Issue 10-11

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Abstract

An enzymatic selective deprotection of methylthiomethyl esters via their sulfone derivatives in presence of labile carbamoyloxy as well as sulfamoyloxy functionalities lead to the formation of O-(carbamoyl) and O-(sulfamoyl)salicylic acids respectively.

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Enzymatic Deprotection of Methylthiomethyl Esters: Synthesis of O-(Carbamoyl) and O-(Sulfamoyl)salicylic Acids

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Enzymatic Deprotection of Methylthiomethyl Esters: Synthesis of O-(Carbamoyl) and O-(Sulfamoyl)salicylic Acids

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