@article { ISI:000311926100005,
	title = {Total synthesis of (-)-isatisine A},
	journal = {Journal of Organic Chemistry},
	volume = {77},
	number = {23},
	year = {2012},
	month = {DEC},
	pages = {10509-10515},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A modular total synthesis of (-)-isatisine A is described in which four consecutive metal-mediated transformations have been employed at the final stage. These include [Pd]-catalyzed Sonogashira coupling, [Pd]-catalyzed nitroalkyne cycloisomerization leading to isatogens, and addition of indoles to isatogens using InCl3- and [Rh]-catalyzed oxidative N-heterocyclization of amino alcohol to form the key amide bond. In addition to these, the removal of the protecting groups has also been carried out in a selective fashion employing either catalytic or stoichiometric metal/metal-based reagents.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo302198v},
	author = {Patel, Pitambar and Ramana, C. V.}
}
