Verdazyl Radical Building Blocks: Synthesis, Structure, and Sonogashira Cross-Coupling Reactions

Podrobná bibliografie
Parent link:European Journal of Organic Chemistry
Vol. 2018, iss. 34.— 2018.— [P. 4802-4811]
Korporativní autor: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Další autoři: Petunin P. V. Pavel Vasilievich, Martynko E. A. Ekaterina Andreevna, Trusova M. E. Marina Evgenievna, Kazantsev M. S. Maksim Sergeevich, Rybalova T. V. Tatjyana Valerjevna, Valiev R. R. Rashid Rinatovich, Uvarov M. N. Mikhail Nikolaevich, Mostovich E. A. Evgeny Alekseevich, Postnikov P. S. Pavel Sergeevich
Shrnutí:Title screen
A general and effective method for the synthesis of 3?phenylveradzyl radicals bearing a variety of iodophenyl substituents has been developed. The synthesized radicals have been characterized by ESR, UV/Vis spectroscopy, and cyclic voltammetry. Structures of biphenyl?substituted radicals have been solved by X?ray crystal structure analysis. The synthesized iodoverdazyls are applicable in the Sonogashira coupling reaction for the preparation of a wide range of ethynyl derivatives. Both N?2 and C?6 substituents were functionalized through Sonogashira coupling.
Режим доступа: по договору с организацией-держателем ресурса
Jazyk:angličtina
Vydáno: 2018
Témata:
On-line přístup:https://doi.org/10.1002/ejoc.201701783
Médium: Elektronický zdroj Kapitola
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=659475

MARC

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330 |a A general and effective method for the synthesis of 3?phenylveradzyl radicals bearing a variety of iodophenyl substituents has been developed. The synthesized radicals have been characterized by ESR, UV/Vis spectroscopy, and cyclic voltammetry. Structures of biphenyl?substituted radicals have been solved by X?ray crystal structure analysis. The synthesized iodoverdazyls are applicable in the Sonogashira coupling reaction for the preparation of a wide range of ethynyl derivatives. Both N?2 and C?6 substituents were functionalized through Sonogashira coupling. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t European Journal of Organic Chemistry 
463 |t Vol. 2018, iss. 34  |v [P. 4802-4811]  |d 2018 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a verdazyl radicals 
610 1 |a nitrogen heterocycles 
610 1 |a cross‐coupling 
610 1 |a density functional calculations 
610 1 |a вердазильные радикалы 
610 1 |a гетероциклы 
610 1 |a кросс-средства 
610 1 |a расчеты 
701 1 |a Petunin  |b P. V.  |c chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1982-  |g Pavel Vasilievich  |3 (RuTPU)RU\TPU\pers\36904  |9 19933 
701 1 |a Martynko  |b E. A.  |g Ekaterina Andreevna 
701 1 |a Trusova  |b M. E.  |c organic chemist  |c Associate professor of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1982-  |g Marina Evgenievna  |3 (RuTPU)RU\TPU\pers\31823  |9 15918 
701 1 |a Kazantsev  |b M. S.  |g Maksim Sergeevich 
701 1 |a Rybalova  |b T. V.  |g Tatjyana Valerjevna 
701 1 |a Valiev  |b R. R.  |c chemist  |c Assistant of Tomsk Polytechnic University  |f 1983-  |g Rashid Rinatovich  |3 (RuTPU)RU\TPU\pers\34114 
701 1 |a Uvarov  |b M. N.  |g Mikhail Nikolaevich 
701 1 |a Mostovich  |b E. A.  |g Evgeny Alekseevich 
701 1 |a Postnikov  |b P. S.  |c organic chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1984-  |g Pavel Sergeevich  |3 (RuTPU)RU\TPU\pers\31287  |9 15465 
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