Reductive cleavage of resin bound arylsulfonates

DOI: 10.1016/S0040-4039(98)00640-6

Source and publish data:

Tetrahedron Letters p. 3651 - 3654 (1998)

Update date:2022-08-29

Topics:

Authors:

Jin, Shujuan

Holub, David P.

Wustrow, David J.

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Article abstract of DOI:10.1016/S0040-4039(98)00640-6

A 4-hydroxybenzoate was tethered to a solid support via an arylsulfonate bond. The carboxylate functionality was converted to a variety of esters and amides. The products were then liberated from the resin by Pd(0) catalyzed reductive cleavage of the arylsulfonate oxygen.

Full text of DOI:10.1016/S0040-4039(98)00640-6

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