@article {2480,
	title = {Enamides and Enesulfonamides as Nucleophiles: Formation of Complex Ring Systems through a Platinum(II)-Catalyzed Addition/Friedel-Crafts Pathway},
	journal = {Journal of Organic Chemistry},
	volume = {74},
	number = {18},
	year = {2009},
	note = {ISI Document Delivery No.: 492LATimes Cited: 5Cited Reference Count: 90Kozak, Jennifer A. Dodd, Jennifer M. Harrison, Tyler J. Jardine, Katherine J. Patrick, Brian O. Dake, Gregory R.},
	month = {Sep},
	pages = {6929-6935},
	type = {Article},
	abstract = {Cyclic enamine derivatives (enesulfonamides and enamides) tethered to an 1-arylalkynyl fragment undergo a platinum(II)-catalyzed tandem alkyne addition/Friedel-Crafts ring closure to form nitrogen-containing polycyclic structures. Regioselectivity in the initial addition of the enesulfonamide or enamide nucleophile to the platinum(II)-alkyne complex is important. Electron-rich arenes and heterocycles led to the formation of products resulting from an Initial 6-endo cyclization. Twenty-three examples of this process are presented.},
	keywords = {CATALYZED CYCLOISOMERIZATIONS, CLOSING, CYCLIZATION ROUTE, DIASTEREOSELECTIVE SYNTHESIS, ELECTRON-RICH OLEFINS, ENANTIOSELECTIVE REACTIONS, LYCOPODIUM ALKALOIDS, METATHESIS, N-ACYL-ENAMINES, NITROGEN-HETEROCYCLES, REARRANGEMENTS, SKELETAL},
	isbn = {0022-3263},
	url = {<Go to ISI>://000269656400004},
	author = {Kozak, J. A. and Dodd, J. M. and Harrison, T. J. and Jardine, K. J. and Patrick, B. O. and Dake, G. R.}
}
@article {2130,
	title = {Total synthesis of (+)-fawcettidine},
	journal = {Angewandte Chemie-International Edition},
	volume = {47},
	number = {22},
	year = {2008},
	note = {ISI Document Delivery No.: 306QCTimes Cited: 22Cited Reference Count: 31Kozak, Jennifer A. Dake, Gregory R.},
	pages = {4221-4223},
	type = {Article},
	keywords = {ALKALOIDS, CATALYSIS, FAWCETTIMINE, GOLD, homogeneous catalysis, LYCOPODIUM ALKALOIDS, platinum, total synthesis},
	isbn = {1433-7851},
	url = {<Go to ISI>://000256261900037},
	author = {Kozak, J. A. and Dake, G. R.}
}
