@article {2491,
	title = {The Direct Synthesis of Unsymmetrical Vicinal Diamines from Terminal Alkynes: A Tandem Sequential Approach for the Synthesis of Imidazolidinones},
	journal = {Synthesis-Stuttgart},
	number = {1},
	year = {2009},
	note = {ISI Document Delivery No.: 395LSTimes Cited: 6Cited Reference Count: 84Lee, Alison V. Sajitz, Melanie Schafer, Laurel L.Sp. Iss. SI},
	month = {Jan},
	pages = {97-104},
	type = {Article},
	abstract = {The combination of titanium-catalyzed anti-Markovnikov hydroamination of terminal alkynes with the Strecker reaction is used in the synthesis of unsymmetrical vicinal diamines via the one-pot synthesis of alpha-cyanoamines. This methodology is Further applied to the efficient synthesis of imidazolidinones. An easy-to-use bis(amidate)titanium precatalyst permits efficient approaches to heterocyclic chemistry from terminal alkynes.},
	keywords = {AMINES, ANTI-MARKOVNIKOV, ASYMMETRIC-SYNTHESIS, CATALYZED INTERMOLECULAR HYDROAMINATION, HETEROCYCLES, HYDROAMINATION, IMIDO COMPLEXES, INTRAMOLECULAR HYDROAMINATION, LIGANDS, SCOPE, tandem reactions, TITANIUM, TITANIUM PRECATALYST, VINYLARENES},
	isbn = {0039-7881},
	url = {<Go to ISI>://000262526200012},
	author = {Lee, A. V. and Sajitz, M. and Schafer, L. L.}
}
@article {789,
	title = {Anti-Markovnikov intermolecular hydroamination: A bis(amidate) titanium precatalyst for the preparation of reactive aldimines},
	journal = {Organic Letters},
	volume = {5},
	number = {24},
	year = {2003},
	note = {ISI Document Delivery No.: 746CHTimes Cited: 80Cited Reference Count: 25},
	month = {Nov},
	pages = {4733-4736},
	type = {Article},
	abstract = {A bulky bis(N-2{\textquoteright},6{\textquoteright}-diisopropylphenyi(phenyl)-amidate)titanium-bis(diethylamido) complex was identified as a highly active and regloselective precatalyst for the anti-Markovnikov hydroamination of a wide range of terminal alkyl alkynes; with alkylamines. This titanium complex was fully characterized, including its X-ray crystal structure. The reactive aldimine products generated have been further elaborated using one-pot procedures to give substituted amines, aidehydes, and the isoquinoline framework.},
	keywords = {ALKENES, CATALYTIC HYDROAMINATION, COMPLEXES, LIGAND, SCOPE, TERMINAL ALKYNES},
	isbn = {1523-7060},
	url = {<Go to ISI>://000186728600052},
	author = {Zhang, Z. and Schafer, L. L.}
}
