@article {1332,
	title = {Bis(amidate) titanium precatalyst for the intermolecular hydroamination of allenes},
	journal = {Inorganica Chimica Acta},
	volume = {359},
	number = {9},
	year = {2006},
	note = {ISI Document Delivery No.: 052YITimes Cited: 25Cited Reference Count: 64},
	month = {Jun},
	pages = {3097-3102},
	type = {Article},
	abstract = {A bis(amidate)-bis(amido) titanium complex (5) is an efficient precatalyst for the regioselective intermolecular hydroamination of substituted allenes. Arylamines react quickly with a 5 mol\% precatalyst loading at 90 degrees C to give the ketimine product, which can be reduced to give substituted amines. With precatalyst loading of 10 mol\% and temperatures of 120 degrees C alkyl amines can be used as viable substrates for the hydroamination of substituted allenes. (c) 2006 Elsevier B.V. All rights reserved.},
	keywords = {ALKENES, allenes, amidate ligands, AMIDO COMPLEXES, CATALYST, CYCLIZATION, HYDROAMINATION, IMIDO COMPLEXES, INTRAMOLECULAR HYDROAMINATION, NITROGEN-HETEROCYCLES, ORGANOLANTHANIDE-CATALYZED HYDROAMINATION, precatalyst, TERMINAL ALKYNES, titanium complex, UNPROTECTED AMINO OLEFINS, VINYLARENES},
	isbn = {0020-1693},
	url = {<Go to ISI>://000238269600063},
	author = {Ayinla, R. O. and Schafer, L. L.}
}
@article {1456,
	title = {Group 4 bis(pyrimidinoxide) complexes. Investigations of electronic effects in catalytic hydroamination},
	journal = {Organometallics},
	volume = {25},
	number = {22},
	year = {2006},
	note = {ISI Document Delivery No.: 094IJTimes Cited: 22Cited Reference Count: 130Lee, Alison V. Schafer, Laurel L.},
	month = {Oct},
	pages = {5249-5254},
	type = {Review},
	abstract = {Substituted pyrimidinols, acidic aromatic alcohols, were used as proligands to synthesize metal complexes of Ti and Zr. These new pseudotetrahedral complexes were investigated as catalysts for the hydroamination of alkynes and alkenes. The stabilized anion of the pyrimidinoxide ligand results in enhanced electrophilicity at the metal center. These electronically modified complexes are catalytically active, but their enhanced reactivity results in reduced selectivity in comparison with the related bis(phenoxide) complexes in alkyne hydroamination. This reactivity was used to advantage in the cyclohydroamination of select aminoalkene substrates with the Zr bis(pyrimidinoxide) complex.},
	keywords = {ALKENES, ANTI-MARKOVNIKOV HYDROAMINATION, ARYLOXIDE, BIS(AMIDATE) TITANIUM PRECATALYST, HYDROAMINATION, IMIDO COMPLEXES, INTERMOLECULAR, LIGANDS, MEDIATED INTRAMOLECULAR, OXIDATIVE AMINATION, TERMINAL ALKYNES},
	isbn = {0276-7333},
	url = {<Go to ISI>://000241232800013},
	author = {Lee, A. V. and Schafer, L. L.}
}
@article {1475,
	title = {Substituent effects in the hydrosilylation of coordinated dinitrogen in a ditantalum complex: Cleavage and functionalization of N-2},
	journal = {Journal of the American Chemical Society},
	volume = {128},
	number = {29},
	year = {2006},
	note = {ISI Document Delivery No.: 064WLTimes Cited: 19Cited Reference Count: 44MacKay, Bruce A. Munha, Rui F. Fryzuk, Michael D.},
	month = {Jul},
	pages = {9472-9483},
	type = {Article},
	abstract = {{The dinitrogen complex ([NPN]Ta)(2)(mu(1)-eta(2):eta(2)-N-2)(mu-H)(2), 1, (where [NPN] = (PhNSiMe2CH2)(2)PPh) undergoes hydrosilylation with primary and secondary alkyl- and arylsilanes, giving a new N-Si bond and a new terminal tantalum hydride derived from one Si-H unit. Various primary silanes can be employed to give isolable complexes of the general formula ([NPN]TaH)(mu-N-N-SiHnR3-n)(mu-H)(2)(Ta[NPN]) (5},
	keywords = {CATALYTIC-REDUCTION, END-ON, LIGAND, METAL-COMPLEXES, MOLECULAR NITROGEN, MOLYBDENUM, N BOND-CLEAVAGE, SIDE-ON, TERMINAL ALKYNES, TRIAMIDOAMINE COMPLEXES},
	isbn = {0002-7863},
	url = {<Go to ISI>://000239120700063},
	author = {MacKay, B. A. and Munha, R. F. and Fryzuk,Michael D.}
}
@article {667,
	title = {Amidate complexes of titanium and zirconium: a new class of tunable precatalysts for the hydroamination of alkynes},
	journal = {Chemical Communications},
	number = {19},
	year = {2003},
	note = {ISI Document Delivery No.: 733YYTimes Cited: 71Cited Reference Count: 25},
	month = {Oct},
	pages = {2462-2463},
	type = {Article},
	abstract = {A series of bis(amidate)group 4-bis(amido) complexes have been prepared, characterized and have been shown to be highly tunable precatalysts for both the intra- and intermolecular hydroamination of alkynes.},
	keywords = {AMIDES, ANILINES, CATALYZED INTERMOLECULAR HYDROAMINATION, COORDINATION, INTRAMOLECULAR HYDROAMINATION/CYCLIZATION, LIGAND, TERMINAL ALKYNES},
	isbn = {1359-7345},
	url = {<Go to ISI>://000186029500034},
	author = {Li, C. Y. and Thomson, R. K. and Gillon, B. and Patrick, B. O. 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.}
}
