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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 26, 1996 - Issue 1
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Original Articles

Synthesis of α-Sulfenamino Nitriles via Trimethylsilylcyanation of Sulfenimines Derived from (+)-CamphorFootnote

, , &
Pages 63-66 | Received 16 May 1995, Published online: 21 Aug 2006
 

Abstract

Optically active α-sulfenamino nitriles were synthesized by using trimethylsilylcyanation of sulfenimines derived from (+)-camphor. The α-sulfenamino nitriles may be hydrolyzed by acid to give α-amino acids.

∗This project was supported by the National Nature Science Foundation of China and the Union Laboratory of Asymmetric Synthesis (Chengdu Institute of Organic Chemistry, Academia Sinica; Hong Kong Polytechinic; Kuo Ching Chemical Co., Ltd.).

Notes

∗This project was supported by the National Nature Science Foundation of China and the Union Laboratory of Asymmetric Synthesis (Chengdu Institute of Organic Chemistry, Academia Sinica; Hong Kong Polytechinic; Kuo Ching Chemical Co., Ltd.).

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