Derivatization of an Alkylideneborane with B═C Bond Cleavage

Abstract

We present the synthesis, structural characterization, and reactivity of alkylideneborane 2, supported by π-donating N-heterocyclic imino and σ-donating N-heterocyclic carbene (NHC) ligands. The incorporation of these ligands effectively weakens the B�C bond strength, leading to enhanced reactivity. Consequently, selective cleavage of the B�C bond can be achieved using pyridine-N-oxide, sulfur, and selenium, resulting in the formation of 1,3-dioxa-2,4-diboretane 3, thioxoborane 4, and selenoborane 5, respectively. Furthermore, intriguing B�C bond insertions with CO 2 and CS 2 are observed, affording zwitterionic borenium/ fluorenide 6 and dithiaboretane 7. The former species 6 is readily converted to transient oxoborane and imidazolium enolate, showcasing the bora-Wittig reaction of alkylideneborane. This investigation highlights the potential of alkylideneborane as a versatile building block for synthesizing novel organoboron compounds through unconventional transformations.

Germaborene reactivity study – addition of carbon nucleophiles, cycloaddition reactions, coordination chemistry

“…48–54 The chemistry of Lewis base stabilized alkylideneboranes is also studied intensively with respect to BC bond cleavage, 1,2-dipolar reactivity studies and cycloaddition reactions. 48,55–63…”