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. 2019 Oct 14;55(80):12100-12103.
doi: 10.1039/c9cc06914c. Epub 2019 Sep 20.

1,1-Phosphinoboration of diazomethanes

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1,1-Phosphinoboration of diazomethanes

Alina Trofimova et al. Chem Commun (Camb). .

Abstract

The reactions of the phosphinoboranes Ph2PBMes2, Ph2PBpin, and Ph2PBcat with the diazomethanes Ph2CN2, C12H8CN2, and EtO2CCHN2 are shown to give products of 1,1-phosphinoboration. The products (1-6) are shown to have PNB linkages with three-coordinate boron centers, whereas the products (EtOOC)CNN(PR2)(Bpin) (R = Ph 7, tBu 8) form zwitterionic heterocycles resulting from chelation of the ester carbonyl to boron. DFT calculations show that the reactions are initiated by N-to-B addition followed by 1,2-phosphinyl shift.

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