4.4 Article

A Mild and Efficient Catalytic Strecker Reaction of N-Alkoxycarbonylamino Sulfones with Trimethylsilyl Cyanide Using Indium(III) Chloride: A Facile Synthesis of α-Aminonitriles

Journal

SYNLETT
Volume -, Issue 20, Pages 3133-3136

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0028-1087277

Keywords

Strecker reaction; N-alkoxycarbonylamino sulfones; trimethylsilyl cyanide; protected alpha-aminonitrile; indium(III) chloride

Funding

  1. CSIR, New Delhi

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The Strecker reaction of N-alkoxycarbonylamino sulfones with trimethylsilyl cyanide in the presence of catalytic amount of indium(III) Chloride at room temperature produces the corresponding protected alpha-aminonitriles in high yields.

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