Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents; Beilstein Journal of Organic Chemistry; Vol. 14

Dades bibliogràfiques
Parent link:	Beilstein Journal of Organic Chemistry.— , 2015- Vol. 14.— 2018.— [P. 531-536]
Autor corporatiu:	Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Altres autors:	Shimizu H. Hisato, Yoshimura A. Akira, Noguchi K. Keiichi, Nemykin V. N. Victor, Zhdankin V. V. Viktor, Saito A. Akio
Sumari:	Title screen [Bis(trifluoroacetoxy)iodo]benzene (BTI) and (diacetoxyiodo)benzene (DIB) efficiently promote the formation of acylnitroso species from hydroxamic acids in the presence of various dienes to give the corresponding hetero-Diels-Alder (HDA) adducts in moderate to high yields. The present method could be applied to the HDA reactions of acylnitroso species with o-benzoquinones generated by the oxidative dearomatization of guaiacols.
Idioma:	anglès
Publicat:	2018
Matèries:	электронный ресурс труды учёных ТПУ acylnitroso benzoquinone cycloaddition dearomatization iodine(III) деароматизация циклоприсоединение йод реагенты
Accés en línia:	https://doi.org/10.3762/bjoc.14.39
Format:	Electrònic Capítol de llibre
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=664363

Descripció
Sumari:	Title screen [Bis(trifluoroacetoxy)iodo]benzene (BTI) and (diacetoxyiodo)benzene (DIB) efficiently promote the formation of acylnitroso species from hydroxamic acids in the presence of various dienes to give the corresponding hetero-Diels-Alder (HDA) adducts in moderate to high yields. The present method could be applied to the HDA reactions of acylnitroso species with o-benzoquinones generated by the oxidative dearomatization of guaiacols.
DOI:	10.3762/bjoc.14.39

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