Single step synthesis of 2,4-dicyanonaphthylamines from synthetic equivalents of α-cyanoalkynes
Abstract
Nitrile thioethers R–CBr![[double bond, length half m-dash]](https://www.rsc.org/images/entities/char_e006.gif)
C(SEt)CN 4 react like α-alkynenitriles with ambiphilic derivatives, as shown by a new synthesis of naphthylamines.
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Article information
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J. Chem. Soc., Chem. Commun., 1991, 1419-1420
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Single step synthesis of 2,4-dicyanonaphthylamines from synthetic equivalents of α-cyanoalkynes
D. Reux and F. Pochat, J. Chem. Soc., Chem. Commun., 1991, 1419 DOI: 10.1039/C39910001419
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