Isoda, Motoyuki’s team published research in Journal of Organic Chemistry in 2021-01-15 | 576-83-0

Journal of Organic Chemistry published new progress about Alkylation, chemoselective. 576-83-0 belongs to class bromides-buliding-blocks, and the molecular formula is C9H11Br, Electric Literature of 576-83-0.

Isoda, Motoyuki; Uetake, Yuta; Takimoto, Tadashi; Tsuda, Junpei; Hosoya, Takamitsu; Niwa, Takashi published the artcile< Convergent Synthesis of Fluoroalkenes Using a Dual-Reactive Unit>, Electric Literature of 576-83-0, the main research area is aryl bromide arylboronicacid palladium catalyst chemoselective reaction; fluoroalkene preparation.

For the synthesis of diverse fluoroalkenes, a dual-reactive C2-unit, (Z)-1-boryl-1-fluoro-2-tosyloxyethene, containing nucleophilic and electrophilic moieties method was developed. Consecutive palladium-catalyzed cross-coupling reactions of this unit with aryl bromides and aryl boronic acids allow for the convergent synthesis of diverse trans-1,2-diaryl-substituted fluoroethenes in a chemoselective and stereoretentive manner.

Journal of Organic Chemistry published new progress about Alkylation, chemoselective. 576-83-0 belongs to class bromides-buliding-blocks, and the molecular formula is C9H11Br, Electric Literature of 576-83-0.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary