Pseudocyclic Arylbenziodoxaboroles as Water-Triggered Aryne Precursors in Reactions with Organic Sulfides

Bibliografiska uppgifter
Parent link:Organic Letters.— .— Washington: ACS Publications
Vol. 26, iss. 9.— 2024.— P. 1891-1895
Institutionell upphovsman: National Research Tomsk Polytechnic University
Övriga upphovsmän: Yoshimura A. Akira, Kim Ngo, Mironova I. A. Irina Andreevna, Gardner Z. S. Zachary, Rohde G. T. Gregory, Nami Ogura, Ueki A. Akiharu, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Saito A. Akio, Zhdankin V. V. Viktor Vladimirovich
Sammanfattning:Title screen
Pseudocyclic arylbenziodoxaboroles are unique aryne precursors under neutral aqueous conditions that selectively react with organic sulfides, forming the corresponding sulfonium salts. This reaction is compatible with various substituents (alkyl, halogen, CN, NO2, CHO, and cyclopropyl) in the aromatic ring or alkyl group of the sulfide. Similar reactions of sulfoxides afford o-hydroxy-substituted sulfonium salts. The structures of key products were confirmed by X-ray analysis.
Текстовый файл
Språk:engelska
Publicerad: 2024
Ämnen:
Länkar:https://doi.org/10.1021/acs.orglett.4c00197
Materialtyp: Elektronisk Bokavsnitt
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=672080

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