@article {2352,
	title = {An Improved Synthesis of Pyridine-Thiazole Cores of Thiopeptide Antibiotics},
	journal = {Journal of Organic Chemistry},
	volume = {74},
	number = {15},
	year = {2009},
	note = {ISI Document Delivery No.: 476XOTimes Cited: 4Cited Reference Count: 29Aulakh, Virender S. Ciufolini, Marco A.},
	month = {Aug},
	pages = {5750-5753},
	type = {Article},
	abstract = {The oxidation of 2-methylthiazoles to 2-formylthiazoles simplifies the implementation of the Bagley variant of the Bohlmann-Rahtz reaction as a key step in a concise new route to pyridine cores of thiopeptide antibiotics.},
	keywords = {1ST, AMYTHIAMICIN-D, CONSTRUCTION, GE2270-A, KEY BUILDING-BLOCKS, macrocycle, MICROCOCCIN P1, ONE-POT, PROMOTHIOCIN, SYNTHESIS, THIOSTREPTON},
	isbn = {0022-3263},
	url = {<Go to ISI>://000268480300104},
	author = {Aulakh, V. S. and Ciufolini,Marco A.}
}
@article {1411,
	title = {Pyrrole synthesis catalyzed by AgOTf or cationic Au(I) complexes},
	journal = {Journal of Organic Chemistry},
	volume = {71},
	number = {12},
	year = {2006},
	note = {ISI Document Delivery No.: 049PTTimes Cited: 65Cited Reference Count: 71Harrison, Tyler J. Kozak, Jennifer A. Corbella-Pane, Montserrat Dake, Gregory R.},
	month = {Jun},
	pages = {4525-4529},
	type = {Article},
	abstract = {Either silver trifluoromethanesulfonate or a mixture of gold( I) chloride, silver trifluoromethanesulfonate, and triphenylphosphine catalyze the formation of pyrroles from substituted beta-alkynyl ketones and amines. The reactions proceed by using 5 mol \% of catalyst with yields of isolated pyrroles ranging from 13\% to 92\%. Sixteen examples are used to compare the effectiveness of each catalyst.},
	keywords = {2-PROPYNYL-1, 3-DICARBONYL COMPOUNDS, AMINATION/ANNULATION REACTIONS, C-H BONDS, CARBOXYLIC-ACIDS, DERIVATIVES, EFFICIENT SYNTHESIS, FURANS, ONE-POT, PYRROLES, REGIOSELECTIVE SYNTHESIS, SUBSTITUTED},
	isbn = {0022-3263},
	url = {<Go to ISI>://000238029300023},
	author = {Harrison, T. J. and Kozak, J. A. and Corbella-Pane, M. and Dake, G. R.}
}
