Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents; Beilstein Journal of Organic Chemistry; Vol. 14
| Parent link: | Beilstein Journal of Organic Chemistry.— , 2015- Vol. 14.— 2018.— [P. 531-536] |
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| Údar corparáideach: | |
| Rannpháirtithe: | , , , , , |
| Achoimre: | 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. |
| Teanga: | Béarla |
| Foilsithe / Cruthaithe: |
2018
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| Ábhair: | |
| Rochtain ar líne: | https://doi.org/10.3762/bjoc.14.39 |
| Formáid: | Leictreonach Caibidil leabhair |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=664363 |
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| 200 | 1 | |a Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents |f H. Shimizu, A. Yoshimura, K. Noguchi [et al.] | |
| 203 | |a Text |c electronic | ||
| 300 | |a Title 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 | |t Beilstein Journal of Organic Chemistry |d 2015- | ||
| 463 | |t Vol. 14 |v [P. 531-536] |d 2018 | ||
| 610 | 1 | |a электронный ресурс | |
| 610 | 1 | |a труды учёных ТПУ | |
| 610 | 1 | |a acylnitroso | |
| 610 | 1 | |a benzoquinone | |
| 610 | 1 | |a cycloaddition | |
| 610 | 1 | |a dearomatization | |
| 610 | 1 | |a iodine(III) | |
| 610 | 1 | |a деароматизация | |
| 610 | 1 | |a циклоприсоединение | |
| 610 | 1 | |a йод | |
| 610 | 1 | |a реагенты | |
| 701 | 1 | |a Shimizu |b H. |g Hisato | |
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| 701 | 1 | |a Noguchi |b K. |g Keiichi | |
| 701 | 1 | |a Nemykin |b V. N. |g Victor | |
| 701 | 1 | |a Zhdankin |b V. V. |g Viktor | |
| 701 | 1 | |a Saito |b A. |g Akio | |
| 712 | 0 | 2 | |a Национальный исследовательский Томский политехнический университет |b Исследовательская школа химических и биомедицинских технологий (ИШХБМТ) |c (2017- ) |3 (RuTPU)RU\TPU\col\23537 |
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