Reactivity of a Sterically Unencumbered α-Borylated Phosphorus Ylide towards Small Molecules

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Abstract

The influence of substituents on α-borylated phosphorus ylides (α-BCPs) has been investigated in a combined experimental and quantum chemical approach. The synthesis and characterization of Me3PC(H)B(iBu)2 (1), consisting of small Me substituents on phosphorous and iBu residues on boron, is reported. Compound 1 is accessible through a novel synthetic approach, which has been further elucidated through DFT studies. The reactivity of 1 towards various small molecules was probed and compared with that of a previously published derivative, Ph3PC(Me)BEt2 (2). Both α-BCPs react with NH3 to undergo heterolytic N−H bond cleavage. Different di- and trimeric ring structures were observed in the reaction products of 1 with CO and CO2. With PhNCO and PHNCS, the expected insertion products [Me3PC(H)(PhNCO)B(iBu)2] and [Me3PC(H)(PhNCS)B(iBu)2], respectively, were isolated.

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Radius, M., Sattler, E., Berberich, H., & Breher, F. (2019). Reactivity of a Sterically Unencumbered α-Borylated Phosphorus Ylide towards Small Molecules. Chemistry - A European Journal, 25(52), 12206–12213. https://doi.org/10.1002/chem.201902681

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