The N-alkoxyindole intermediate then undergoes intramolecular heterocyclization, which involves the formation of a new ring structure within the molecule. This ring formation results in the formation of the desired N-alkoxyindole-3-carbonitrile.
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1-methoxy-2-phenyl-1H-indole-3-carbonitrile
(S)-2-(t-butoxycarbonylamino)-N-methyl-2-phenyl-N-(1,2-propadienyl)acetamide
Methyl-3-methylbenzo[c]isoxazole-6-carboxylate
1-methyl-4-phenylethynylpyrazole-5-hydroxamic acid
4-(N,N'-diphenyl)guanidino-2methyl-5-methylthio-2H-1,2,4-triazole-3(4H)-thione
3-Nitroisoxazole-5-carboxaMide
