Wang, Yan’s team published research in Australian Journal of Chemistry in 2014 | CAS: 1061367-22-3

Australian Journal of Chemistry published new progress about Borylation (regioselective). 1061367-22-3 belongs to class chlorides-buliding-blocks, name is 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C13H18BClO3, Safety of 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Wang, Yan published the artcileTransition Metal-Free Synthesis of Pinacol Arylboronate: Regioselective Boronation of 1,3-Disubstituted Benzenes, Safety of 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, the main research area is pinacol arylboronate preparation; regioselective boronation disubstituted benzene.

The regioselective synthesis of pinacol arylboronate has been achieved from 1,3-disubstituted benzene through directed ortho-metalation (DoM)-borylation sequence. A wide range of substituents and borylating reagents were investigated. In situ lithiation and subsequent boronation predominantly occurred at the ortho-position to afford the desired products in moderate yields.

Australian Journal of Chemistry published new progress about Borylation (regioselective). 1061367-22-3 belongs to class chlorides-buliding-blocks, name is 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C13H18BClO3, Safety of 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Ito, Motoki’s team published research in Angewandte Chemie, International Edition in 2012 | CAS: 1061367-22-3

Angewandte Chemie, International Edition published new progress about Cross-coupling reaction, regioselective. 1061367-22-3 belongs to class chlorides-buliding-blocks, name is 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C13H18BClO3, Safety of 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Ito, Motoki published the artcileSynthesis of Boron-Substituted Diaryliodonium Salts and Selective Transformation into Functionalized Aryl Boronates, Safety of 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, the main research area is boron substituted iodonium salt preparation cross coupling functionalized aromatic; aryl boronate regioselective aromatic nucleophilic substitution hypervalent iodine.

Diaryliodonium salts were synthesized from aryl boronate derivatives according to two alternative general methods with hypervalent iodine(III) reagents and fluoroalc. solvents: transformation of an aryl C-H bond and boron-iodine(III) exchange. The salts could be functionalized by both catalyst-free and metal-catalyzed reactions without loss of the boron functionality.

Angewandte Chemie, International Edition published new progress about Cross-coupling reaction, regioselective. 1061367-22-3 belongs to class chlorides-buliding-blocks, name is 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C13H18BClO3, Safety of 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics