Issue 9, 1998

Scandium triflate-catalyzed Strecker-type reactions of aldehydes, amines and tributyltin cyanide in both organic and aqueous solutions. Achievement of complete recovery of the tin compounds toward environmentally-friendly chemical processes

Abstract

Scandium triflate (CF3SO3)-catalyzed Strecker-type reactions were successfully carried out by simply mixing aldehydes, amines and tributyltin cyanide at room temperature, to afford α-amino nitriles in high yields. The reactions proceeded smoothly in both organic and aqueous solutions, and complete recovery of the tin materials has been achieved.

Article information

Article type
Paper

Chem. Commun., 1998, 981-982

Scandium triflate-catalyzed Strecker-type reactions of aldehydes, amines and tributyltin cyanide in both organic and aqueous solutions. Achievement of complete recovery of the tin compounds toward environmentally-friendly chemical processes

S. Kobayashi and T. Busujima, Chem. Commun., 1998, 981 DOI: 10.1039/A801464G

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