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Secondary amine–borane adducts R2NH·BH3, which are stable to H2 elimination below 100 °C, undergo efficient catalytic dehydrocoupling at 25–45 °C in the presence of RhI or RhIII complexes to quantitatively form cyclic aminoboranes NR2–BH22 (1: R = Me or 2: cyclo-C4H8); under similarly mild conditions, the analogous adducts NH3·BH3 and MeNH2·BH3 yield borazines RN–BH3 (3: R = H or 4: R = Me) in yields limited by intermolecular coupling reactions.
Jaska et al. (Mon,) studied this question.