《Facile Synthesis of α-Boryl-Substituted Allylboronate Esters Using Stable Bis[(pinacolato)boryl]methylzinc Reagents》 was published in Organic Letters in 2020. These research results belong to Shin, Minkyeong; Kim, Minjae; Hwang, Chiwon; Lee, Hyojae; Kwon, Hyunchul; Park, Jinyoung; Lee, Eunsung; Cho, Seung Hwan. Computed Properties of C13H26B2O4 The article mentions the following:
Reported herein is the utilization of bis[(pinacolato)boryl]methylzinc halides, whose structures are characterized via single-crystal X-ray anal., as solid storable reagents for copper-catalyzed coupling with vinyliodonium salts. The reaction proceeds under mild conditions and shows broad scope with respect to vinyliodonium salts, affording various α-boryl-substituted allylboronate esters in good yields. Synthetic applications of the obtained products are also demonstrated.Bis[(pinacolato)boryl]methane(cas: 78782-17-9Computed Properties of C13H26B2O4) was used in this study.
Bis[(pinacolato)boryl]methane(cas: 78782-17-9) belongs to organoboron compounds.Computed Properties of C13H26B2O4 Organoboron compounds have been a cornerstone of synthetic transformations for decades. Areas such as boron-containing catalysts, metalate chemistry, photoredox methods, and boryl anions have brought significant new developments in understanding and provided new reactivity upon.
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