Journal of the Chemical Society. Chemical communications p. 149 - 150 (1983)
Update date:2022-08-17
Topics:
Niel, Johannes C. G. van
Pandit, Upendra K.
Reduction of N-cyclopropylmethylenephenylamine by 3,5-diethoxycarbonyl-2,6-dimethyl-1,4-dihydropyridine (Hantzsch ester) results in the exclusive formation of N-cyclopropylmethylaniline, whereas reduction with triphenyltin hydride gives both N-cyclopropylmethylaniline and n-butylaniline, a product of cyclopropane ring cleavage.
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Doi:10.1016/S0022-328X(00)81950-6
(1982)Doi:10.1039/c9ra05576b
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