Enzymatic deprotection of methylthiomethyl esters: Synthesis of O-(carbamoyl) and O-(sulfamoyl)salicylic acids

Article abstract of DOI:10.1080/00397919108021048

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.

Full text of DOI:10.1080/00397919108021048

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Enzymatic Deprotection of
Methylthiomethyl Esters:
Synthesis of O-(Carbamoyl) and
O-(Sulfamoyl)salicylic Acids
Ahmed Kamal a
a Indian Institute of Chemical Technology ,
Hyderabad, 7, India
Published online: 16 Feb 2007.
To cite this article: Ahmed Kamal (1991) Enzymatic Deprotection of Methylthiomethyl
Esters: Synthesis of O-(Carbamoyl) and O-(Sulfamoyl)salicylic Acids, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:10-11, 1293-1299, DOI: 10.1080/00397919108021048
To link to this article: http://dx.doi.org/10.1080/00397919108021048
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