Qiu, Di; Li, Songyi; Yue, Guanglu; Mao, Jinshan; Xu, Bei; Yuan, Xinyu; Ye, Fei published the artcile< Synthesis of arylboronates via the Pd-catalyzed desulfitative coupling reaction of sodium arylsulfinates with bis(pinacolato)diboron>, Quality Control of 112-63-0, the main research area is arylboronate preparation palladium catalyzed desulfitative coupling sodium arylsulfinate pinacolatodiboron; carbon boron bond formation.
The desulfitative borylation reaction of sodium arylsulfinates with bis(pinacolato)diboron or bis(neopentylglycolato)diboron under palladium catalysis has been developed, allowing selective C-B bond formation to give arylboronates with a range of functional groups in moderate to good yields under mild reaction conditions. A gram-scale preparation as well as the cascade Suzuki-Miyaura cross-coupling of arylboronates demonstrated the potential practical utility in organic synthesis.
Tetrahedron Letters published new progress about Bond formation (boron-carbon). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Quality Control of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics