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- W3092804950 abstract "An N-heterocyclic-carbene-stabilized diboryne undergoes rapid, high-yielding and catalyst-free hydroamination reactions with primary amines, yielding 1-amino-2-hydrodiborenes, which can be considered boron analogues of enamines. The electronics of the organic substituent at nitrogen influence the structure and further reactivity of the diborene product. With electron-rich anilines, a second hydroamination can occur at the diborene to generate 1,1-diamino-2,2-dihydrodiboranes. With isopropylamine, the electronic influence of the alkyl substituent upon the diborene leads to an unprecedented boron-mediated intramolecular N-dearylation reaction of an N-heterocyclic carbene unit." @default.
- W3092804950 created "2020-10-22" @default.
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- W3092804950 date "2020-11-09" @default.
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- W3092804950 title "Synthesis of Boron Analogues of Enamines via Hydroamination of a Boron−Boron Triple Bond" @default.
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- W3092804950 doi "https://doi.org/10.1002/anie.202012101" @default.
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