THE CONVERSION OF CARBOXYLIC ACIDS TO AMIDES VIA TIN(II) REAGENTS

DOI: 10.1016/S0040-4039(00)73950-5

Source and publish data:

Tetrahedron Letters p. 5193 - 5196 (1993)

Update date:2022-08-02

Topics: Conversion Amides Carboxylic Acids Experimental terms

Authors:

Burnell-Curty, Cynthia

Roskamp, Eric J.

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Article abstract of DOI:10.1016/S0040-4039(00)73950-5

Unsymmetrical tin(II) amides can be generated, in situ, by adding one equivalent of an amine to bis(bistrimethylamino) tin, Sn2.Treatment of carboxylic acids with these tin(II) reagents derived from alkyl or aryl amines results in smooth conversion to the corresponding N-alkyl or N-aryl amides.

Full text of DOI:10.1016/S0040-4039(00)73950-5

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