Hypervalent Iodine(III) Reagent Mediated Regioselective Cycloaddition of Aldoximes with Enaminones

Hypervalent Iodine(III) Reagent Mediated Regioselective Cycloaddition of Aldoximes with Enaminones

Podrobná bibliografie
Parent link:	European Journal of Organic Chemistry Vol. 2019, iss. 39.— 2019.— [P. 6682-6689]
Korporace:	Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий, Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий Научно-исследовательский центр "Онкотераностика"
Další autoři:	Yoshimura A. Akira, Jarvi M. E. Melissa, Shea M. T. Michael, Makitalo C. L. Cody, Rohde G. T. Gregory, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Saito A. Akio, Zhdankin V. V. Viktor Vladimirovich
Shrnutí:	Title screen An efficient oxidative cycloaddition of enaminones with nitrile oxides generated in situ from respective aldoximes using hypervalent iodine reagents has been developed. Reactions of various aldoximes with enaminones in the presence of [hydroxy(tosyloxy)iodo]benzene involved the regioselective cycloaddition reaction resulting in the formation of the 3,4-disubstituted isoxazoles in moderate to good yields. Structures of several isoxazole products were confirmed by a single X-ray crystallography. Режим доступа: по договору с организацией-держателем ресурса
Jazyk:	angličtina
Vydáno:	2019
Témata:	электронный ресурс труды учёных ТПУ
On-line přístup:	https://doi.org/10.1002/ejoc.201901258
Médium:	Elektronický zdroj Kapitola
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=662836

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