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001 664363
005 20231030041927.0
035 _a(RuTPU)RU\TPU\network\35547
035 _aRU\TPU\network\26532
090 _a664363
100 _a20210412a2018 k y0engy50 ba
101 0 _aeng
135 _adrgn ---uucaa
181 0 _ai
182 0 _ab
200 1 _aOxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents
_fH. Shimizu, A. Yoshimura, K. Noguchi [et al.]
203 _aText
_celectronic
300 _aTitle screen
320 _a[References: 36 tit.]
330 _a[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.
461 _tBeilstein Journal of Organic Chemistry
_d2015-
463 _tVol. 14
_v[P. 531-536]
_d2018
610 1 _aэлектронный ресурс
610 1 _aтруды учёных ТПУ
610 1 _aacylnitroso
610 1 _abenzoquinone
610 1 _acycloaddition
610 1 _adearomatization
610 1 _aiodine(III)
610 1 _aдеароматизация
610 1 _aциклоприсоединение
610 1 _aйод
610 1 _aреагенты
701 1 _aShimizu
_bH.
_gHisato
701 1 _aYoshimura
_bA.
_cchemical engineer
_cProfessor of Tomsk Polytechnic University
_f1981-
_gAkira
_2stltpush
_3(RuTPU)RU\TPU\pers\39852
701 1 _aNoguchi
_bK.
_gKeiichi
701 1 _aNemykin
_bV. N.
_gVictor
701 1 _aZhdankin
_bV. V.
_gViktor
701 1 _aSaito
_bA.
_gAkio
712 0 2 _aНациональный исследовательский Томский политехнический университет
_bИсследовательская школа химических и биомедицинских технологий (ИШХБМТ)
_c(2017- )
_h8120
_2stltpush
_3(RuTPU)RU\TPU\col\23537
801 2 _aRU
_b63413507
_c20210412
_gRCR
856 4 _uhttps://doi.org/10.3762/bjoc.14.39
942 _cCF