Generation of benzyne from aryl benziodoxaborole triflate under aqueous conditions and its reactions with alkyl aryl sulfides; Arkivoc; Vol. 1

Detalles Bibliográficos
Parent link:Arkivoc.— .— New-York: ARKAT USA, Inc.
Vol. 1.— 2024.— Article number 202412213, 11 p.
Autor Corporativo: National Research Tomsk Polytechnic University (570)
Otros Autores: Yoshimura A. Akira, Ngo Kim, Mironova I. A. Irina Andreevna, Gardner S. Zachary, Ogura Nami, Ueki Akiharu, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Saito Akio, Zhdankin V. V. Viktor Vladimirovich
Sumario:Title screen
Mesityl benziodoxaborole triflate is a unique benzyne precursor under aqueous conditions in the presence of NaHCO3 at room temperature. Reactions of alkyl aryl sulfides with benzyne generated under these conditions selectively afford the corresponding sulfonium salts. In contrast, the previously reported reactions of alkyl aryl sulfides with common benzyne precursors under strongly basic anhydrous conditions lead to various products of cyclization, rearrangement, or elimination but not to sulfonium salts. This very mild procedure can be further extended to the preparation of sulfonium salts from diaryl sulfides, dialkyl sulfides, cyclic alkyl and arylsulfides, as well as a selenonium salt from diphenyl selenide.
Текстовый файл
AM_Agreement
Lenguaje:inglés
Publicado: 2024
Materias:
Acceso en línea:https://doi.org/10.24820/ark.5550190.p012.213
Formato: xMaterials Electrónico Capítulo de libro
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=673457

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200 1 |a Generation of benzyne from aryl benziodoxaborole triflate under aqueous conditions and its reactions with alkyl aryl sulfides  |f Akira Yoshimura, Kim Ngo, Irina A. Mironova [et al.]  |d Генерация бензина из арилбензиодоксобол трифлата в водных условиях и его реакции с алкил- и арилсульфидами  |z eng 
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330 |a Mesityl benziodoxaborole triflate is a unique benzyne precursor under aqueous conditions in the presence of NaHCO3 at room temperature. Reactions of alkyl aryl sulfides with benzyne generated under these conditions selectively afford the corresponding sulfonium salts. In contrast, the previously reported reactions of alkyl aryl sulfides with common benzyne precursors under strongly basic anhydrous conditions lead to various products of cyclization, rearrangement, or elimination but not to sulfonium salts. This very mild procedure can be further extended to the preparation of sulfonium salts from diaryl sulfides, dialkyl sulfides, cyclic alkyl and arylsulfides, as well as a selenonium salt from diphenyl selenide. 
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461 1 |t Arkivoc  |c New-York  |n ARKAT USA, Inc. 
463 1 |t Vol. 1  |v Article number 202412213, 11 p.  |d 2024 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a hypervalent iodine 
610 1 |a benziodoxaborole 
610 1 |a benzyne 
610 1 |a iodonium salts 
610 1 |a sulfonium salts 
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