Preparation, structure, and reactivity of ortho-hydroxy-substituted aryliodonium salts, precursors to ortho-iodo-substituted diaryl ethers; Arkivoc; Vol. 4

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Parent link:Arkivoc.— .— New-York: ARKAT USA, Inc.
Vol. 4.— 2025.— Article number 202612556, 19 p.
Korporativní autor: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Další autoři: Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Yoshimura A. Akira, Lyulyaev A. V. Aleksandr Vitaljevich, Mironova I. A. Irina Andreevna, Shurikov M. K. Matvey Konstantinovich, Rode G. T. Gregori, Saito Akio, Zhdankin V. V. Viktor Vladimirovich
Shrnutí:Title screen
ortho-Hydroxy-substituted aryliodonium salts were prepared by a two-step one-pot synthesis based on the reaction of 2-alkoxy-1-[(diacetoxy)iodo]arenes with arylboronic acids involving the initial formation of 2-alkoxyphenyl(aryl)iodonium salts and followed by deprotection of the intermediate product by boron tribromide. This procedure works well with halogen-, cyano-, 2-hydroxy-, 3-hydroxy-, 4-hydroxy-, methyl-, or trifluoromethyl-substituted arylboronic acids. Structures of three 2-hydroxyphenyl(aryl)iodonium bromides were confirmed by single crystal X-ray crystallography. The prepared 2-hydroxyphenyl(aryl)iodonium salts can be further converted to ortho-iodo-substituted diaryl ethers by treatment with a base via intermediate formation of the unstable aryliodonium betaines
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Jazyk:angličtina
Vydáno: 2025
Témata:
On-line přístup:https://doi.org/10.24820/ark.5550190.p012.556
Médium: Elektronický zdroj Kapitola
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=687712