@article {46349,
	title = {Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams},
	journal = {RSC Advances},
	volume = {9},
	year = {2019},
	month = {SEP },
	pages = {30277-30291},
	type = {Article},
	abstract = {<p>Oxone promoted intramolecular dehydrogenative imino Diels-Alder reaction (Povarov cyclization) of alkyne tethered N-aryl glycine esters and amides has been explored, thus affording biologically significant quinoline fused lactones and lactams. The reaction is simple, scalable, and high yielding (up to 88\%). The method was further extended to prepare biologically important luotonin-A analogues and the quinoline core of uncialamycin.</p>
},
	doi = {10.1039/c9ra06212b},
	author = {More, Devidas A. and Shinde, Ganesh H. and Shaikh, Aslam C. and Muthukrishnan, M.}
}
