Zobrazeno 1 - 3
of 3
pro vyhledávání: '"John P. W. Stelmach"'
Publikováno v:
Organometallics. 34:4693-4699
κ5-(Me3SiNCH2CH2)2N(CH2CH2NSiMe2CH2)Zr (1) has been found to dehydrocouple amine borane substrates, RR′NHBH3 (R = R′ = Me; R = tBu, R′ = H; R = R′ = H), at low to moderate catalyst loadings (0.5–5 mol %) and good to excellent conversions,
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 45(14)
Simple tin derivatives, Cp*2SnCl2 (1) and Ph2SnCl2 (2), catalyze the hydrophosphination of alkene substrates with diphenylphosphine. Competitive dehydrocoupling to give Ph4P2 was observed, but this side reaction can be mitigated when the catalysis is
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 44(27)
Two cobalt compounds, Cp*Co(CO)I2 (1) and CpCo(CO)I2 (2) (Cp* = η(5)-C5Me5, Cp = η(5)-C5H5), catalyze the dehydrogenation of ammonia borane under either anaerobic or aerobic conditions and are also effective hydrogenation catalysts for alkenes and