@article {https://doi.org/10.1002/chem.202100014,
	title = {Zirconium Catalyzed Hydroaminoalkylation for the Synthesis of α-Arylated Amines and N-Heterocycles},
	journal = {Chemistry {\textendash} A European Journal},
	volume = {27},
	number = {20},
	year = {2021},
	pages = {6334-6339},
	abstract = {Abstract The zirconium catalyzed hydroaminoalkylation of alkenes with N-aryl- and sterically demanding N-alkyl-α-arylated secondary amines by using commercially available Zr(NMe2)4 is reported. N-phenyl- and N-isopropylbenzylamine are used as amine substrates to establish the alkene substrate scope. Exclusively linear products are obtained in the presence of bulky vinylsilanes. Challenging α-heteroarylated amines and functionalized alkene substrates are compatible with this easy to use catalyst, affording a new disconnection strategy for the atom- and step-economic preparation of selectively substituted saturated α-arylated heterocycles.},
	keywords = {alpha-arylated amines, HETEROCYCLES, HYDROAMINOALKYLATION, ZIRCONIUM},
	doi = {https://doi.org/10.1002/chem.202100014},
	url = {https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202100014},
	author = {Koperniku, Ana and Schafer, Laurel L.}
}
@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 {2493,
	title = {Total Synthesis and Stereochemical Assignment of Micrococcin P1},
	journal = {Angewandte Chemie-International Edition},
	volume = {48},
	number = {23},
	year = {2009},
	note = {ISI Document Delivery No.: 452GHTimes Cited: 11Cited Reference Count: 41Lefranc, David Ciufolini, Marco A.},
	pages = {4198-4201},
	type = {Article},
	keywords = {ACID, antibiotics, CHEMISTRY, DOMAIN, FRAGMENT A-C, GE2270-A, HETEROCYCLES, MICROCOCCIN P1, P-1, PROTEIN-SYNTHESIS, THIOPEPTIDE ANTIBIOTICS, thiopeptides, THIOSTREPTON},
	isbn = {1433-7851},
	url = {<Go to ISI>://000266527800024},
	author = {Lefranc, D. and Ciufolini,Marco A.}
}
@article {2137,
	title = {Synthesis and Enzymatic Incorporation of Modified Deoxyadenosine Triphosphates},
	journal = {European Journal of Organic Chemistry},
	number = {29},
	year = {2008},
	note = {ISI Document Delivery No.: 365YXTimes Cited: 7Cited Reference Count: 35Lam, Curtis Hipolito, Christopher Perrin, David M.},
	month = {Oct},
	pages = {4915-4923},
	type = {Article},
	abstract = {Several deoxyadenosine triphosphates containing modifications at the 8-position have been synthesized. Suitably protected 8-bromodeoxyadenosines were coupled with five imidazole-containing moieties by nucleophilic aromatic substitution or Sonagashira coupling to give modified nucleosides that were then triphosphorylated. Incorporation assays were performed for these modified residues with many commercially available DNA polymerases, and it was found that two of the modified dATPs could be effectively taken up as substrates by Sequenase V2.0. These two residues are candidates for substrates in combinatorial selections in the search for improved catalysis from DNAzymes. ((C) Wiley-VCH Verlag GmbH \& Co. KGaA, 69451 Weinheim, Germany, 2008)},
	keywords = {AMINO-ACID, bioorganic chemistry, CATALYTIC REPERTOIRE, CLEAVING DNA ENZYME, DERIVATIVES, DNA, ENZYMES, FUNCTIONALITIES, HETEROCYCLES, IN-VITRO SELECTION, NUCLEIC-ACIDS, nucleotides, OLIGONUCLEOTIDES, PCR, POLYMERASES, SELEX},
	isbn = {1434-193X},
	url = {<Go to ISI>://000260447200009},
	author = {Lam, C. and Hipolito, C. and Perrin,David M.}
}
@article {947,
	title = {Carbon-nitrogen bond formation via the reaction of terminal alkynes with a dinuclear side-on dinitrogen complex},
	journal = {Journal of the American Chemical Society},
	volume = {126},
	number = {31},
	year = {2004},
	note = {ISI Document Delivery No.: 843TSTimes Cited: 27Cited Reference Count: 21},
	month = {Aug},
	pages = {9480-9481},
	type = {Article},
	keywords = {ACTIVATION, COORDINATION, FIXATION, FUNCTIONALIZATION, HETEROCYCLES, HYDROAMINATION, METAL-COMPLEXES, MOLECULAR NITROGEN, MOLYBDENUM, N-2},
	isbn = {0002-7863},
	url = {<Go to ISI>://000223110100007},
	author = {Morello, L. and Love, J. B. and Patrick, B. O. and Fryzuk,Michael D.}
}
