Abstract
1. Dialkylboryl-β-diiminates with an aryl group on the nitrogen atom of the chelate ring were synthesized by the reaction between vinylaminodialkylboranes and nitriles. β-Diiminates with an acetoxy or methoxy group on the boron atom were prepared by nucleophilic substitution at the boron atom. 2. In the mass spectra of dialkylboryl-β-diiminates, ions which are formed by loss of an alkyl group from the boron atom give rise to peaks with the greatest intensity.
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