The regioselective hydroamination of propargylguanidines involves the addition of an amino group (-NH2) across the alkyne bond. The nitrogen in the guanidine group also participates in this transformation.
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N-(4-methoxybenzyl)-3-phenylprop-2-yn-1-amine hydrochloride
(E)-2-(2-cyclohexylvinyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
2-AMINO-4-PHENYLPHENOL
2-methyl-4-phenyl-1-(2-o-tolylethylidene)semicarbazide
2-bromo-1,1-diphenyl-3-methylbutene
(Z)-4-{[1-(1-methyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-3-oxo-3-phenylprop-1-en-1-yl]amino}butanoic acid
2-methyl-4-phenyl-1-(2-o-tolylethylidene)semicarbazide
benzyl 2-(N-allyl-2,2,2-trifluoroacetamido)ethylcarbamate
4-fluoro-N-(1-phenylpropyl)aniline
N-cyclohexyl-1,1-dimethyl-L-valinol
1-(4-Methyl-phenyl)-1-(2-amino-phenyl)-aethan
4-methyl-N-(prop-2-yn-1-ylcarbamoyl)benzenesulfonamide
(2S,3R)-3-ethyl-2-methyl-1-tosylaziridine-2-carbaldehyde
2-(tert-butyl)-N-(1-phenylethyl)aniline
Benzenemethanamine, N-(2-phenylethylidene)-
C25H17BrN2
Benzeneethanamine, a-3-butenyl-
(3,3-dimethylbutan-2-ylidene)hydrazine
2,4-dibromo-6-(1-phenylethyl)aniline
Morpholine, 4-[1-(4-methoxyphenyl)pentyl]-
