@article {1060,
	title = {Intramolecular hydroamination of unactived olefins with Ti(NMe2)(4) as a precatalyst},
	journal = {Organic Letters},
	volume = {7},
	number = {10},
	year = {2005},
	note = {ISI Document Delivery No.: 924NCTimes Cited: 104Cited Reference Count: 59},
	month = {May},
	pages = {1959-1962},
	type = {Article},
	abstract = {[GRAPHICS] Commercially available Ti(NMe2)(4) has been used effectively as a precatalyst in a facile protocol for the intramolecular hydroamination of aminoalkenes to yield pyrrolidine and piperidine heterocyclic products with isolated yields up to 92\%. Germinally substituted substrates display the highest reactivity. This precatalyst is also effective for the hydroamination of activated internal alkenes, providing access to more complex heterocyclic target molecules.},
	keywords = {ALKENE HYDROAMINATION, ALKYNE, AMIDO COMPLEXES, ANTI-MARKOVNIKOV, CATALYZED INTERMOLECULAR HYDROAMINATION, GROUP-3 METALS, HYDROAMINATION, IMIDO COMPLEXES, REACTIVITY, TITANIUM, ZIRCONIUM},
	isbn = {1523-7060},
	url = {<Go to ISI>://000228984500019},
	author = {Bexrud, J. A. and Beard, J. D. and Leitch, D. C. and Schafer, L. L.}
}
@article {922,
	title = {Scandium-catalyzed intramolecular hydroamination. Development of a highly active cationic catalyst},
	journal = {Organometallics},
	volume = {23},
	number = {10},
	year = {2004},
	note = {ISI Document Delivery No.: 818FNTimes Cited: 100Cited Reference Count: 37},
	month = {May},
	pages = {2234-2237},
	type = {Article},
	abstract = {The scandium-catalyzed intramolecular hydroamination of alkynes and alkenes is reported. Complex structure/catalyst activity investigations resulted in the identification of a highly catalytically active cationic, beta-diketiminato scandium complex.},
	keywords = {ALKENES, ALKYNES, AMIDO COMPLEXES, BETA-DIKETIMINATO LIGANDS, DERIVATIVES, GROUP-3 METALS, ORGANOSCANDIUM, REACTIVITY, YTTRIUM, ZIRCONIUM},
	isbn = {0276-7333},
	url = {<Go to ISI>://000221231100006},
	author = {Lauterwasser, F. and Hayes, P. G. and Brase, S. and Piers, W. E. and Schafer, L. L.}
}
