Preparation, Structure, and Reactivity of Pseudocyclic β-Trifluorosulfonyloxy Vinylbenziodoxolone Derivatives; Advanced Synthesis and Catalysis; Vol. 363, iss. 13

Detaylı Bibliyografya
Parent link:Advanced Synthesis and Catalysis
Vol. 363, iss. 13.— 2021.— [P. 3365-3371]
Müşterek Yazar: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Diğer Yazarlar: Yoshimura A. Akira, Huss Ch. D. Christopher, Mackenzie L. Liebl, Rohde G. L. Gregory, Larson S. M. Scott, Frahm G. B. Gunnar, Mattew W. L. W. Luedtke, Tanner J. Sh. J. Schumacher, Gardner S., Zhdankin V. V. Viktor Vladimirovich, Postnikov P. S. Pavel Sergeevich, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Tsugio K. Kitamura, Saito A. Akio
Özet:Title screen
Pseudocyclic β-trifluorosulfonyloxy vinylbenziodoxolones were prepared starting from hydroxybenziodoxolones and alkynes in the presence of trifluoromethanesulfonic acid. The reaction of these compounds with azide anion leads to β-azido vinylbenziodoxolones as products of vinylic nucleophilic substitution in which addition-elimination reactions occur and the double bond configuration is retained. The structures of β-trifluorosulfonyloxy vinylbenziodoxolone and β-azido vinylbenziodoxolone were established by single crystal X-ray diffraction.
Dil:İngilizce
Baskı/Yayın Bilgisi: 2021
Konular:
Online Erişim:https://doi.org/10.1002/adsc.202100341
Materyal Türü: Elektronik Kitap Bölümü
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667947

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200 1 |a Preparation, Structure, and Reactivity of Pseudocyclic β-Trifluorosulfonyloxy Vinylbenziodoxolone Derivatives  |f A. Yoshimura, Ch. D. Huss, L. Mackenzie [et al.] 
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330 |a Pseudocyclic β-trifluorosulfonyloxy vinylbenziodoxolones were prepared starting from hydroxybenziodoxolones and alkynes in the presence of trifluoromethanesulfonic acid. The reaction of these compounds with azide anion leads to β-azido vinylbenziodoxolones as products of vinylic nucleophilic substitution in which addition-elimination reactions occur and the double bond configuration is retained. The structures of β-trifluorosulfonyloxy vinylbenziodoxolone and β-azido vinylbenziodoxolone were established by single crystal X-ray diffraction. 
461 |t Advanced Synthesis and Catalysis 
463 |t Vol. 363, iss. 13  |v [P. 3365-3371]  |d 2021 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a hypervalent iodine 
610 1 |a vinylbenziodoxolones 
610 1 |a alkenyliodonium 
610 1 |a pseudocyclic 
610 1 |a Micheal acceptor 
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701 1 |a Huss  |b Ch. D.  |g Christopher 
701 1 |a Mackenzie  |b L.  |g Liebl 
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701 1 |a Larson  |b S. M.  |g Scott 
701 1 |a Frahm  |b G. B.  |g Gunnar 
701 1 |a Mattew  |b W. L.  |g W. Luedtke 
701 1 |a Tanner  |b J. Sh.  |g J. Schumacher 
701 1 |a Gardner  |b S. 
701 1 |a Zhdankin  |b V. V.  |c химик  |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences  |f 1956-  |g Viktor Vladimirovich  |3 (RuTPU)RU\TPU\pers\35758 
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 
701 1 |a Yusubov  |b M. S.  |c chemist  |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences  |f 1961-  |g Mekhman Suleiman-Ogly (Suleimanovich)  |3 (RuTPU)RU\TPU\pers\31833  |9 15928 
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