Nitropyridines as 2π-Partners in 1,3-Dipolar Cycloadditions with N-Methyl Azomethine Ylide: An Easy Access to Condensed Pyrrolines

1,3-Dipolar cycloaddition reactions of 2-substituted 5-<i>R</i>-3-nitropyridines and isomeric 3-<i>R</i>-5-nitropyridines with N-methyl azomethine ylide were studied. The effect of the substituent at positions 2 and 5 of the pyridine ring on the possibility of the [3+2]-cycloaddition process was rev...

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Hlavní autoři:	Maxim A. Bastrakov, Alexey K. Fedorenko, Alexey M. Starosotnikov, Alexander Kh. Shakhnes
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	MDPI AG 2021-09-01
Edice:	Molecules
Témata:	nitro group nitropyridines pyrrolo[3,4-<i>c</i>]pyridines dearomatization 1,3-dipolar cycloadditition pyrrolidines
On-line přístup:	https://www.mdpi.com/1420-3049/26/18/5547
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