@article { ISI:000247278400009,
	title = {Enantioselective synthesis of tarchonanthuslactone using proline-catalyzed asymmetric alpha-aminooxylation},
	journal = {Tetrahedron-Asymmetry},
	volume = {18},
	number = {8},
	year = {2007},
	month = {MAY},
	pages = {975-981},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A practical enantio selective synthesis of tarchonanthuslactone 1, an important natural product with a polyol unit, is described. The sequence of synthetic reactions involves proline-catalyzed alpha-aminooxylation and iodine-induced electrophilic cyclization as the chiral inducing steps. (c) 2007 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2007.04.008},
	author = {George, Shyla and Sudalai, Arurnugam}
}
@article { ISI:000265330500010,
	title = {Concise enantioselective synthesis of 1-[(S)-3-(dimethylamino)-3,4 dihydro-6,7-dimethoxyquinolin-1(2H)-yl]propan-1-one, (S)-903},
	journal = {Tetrahedron-Asymmetry},
	volume = {20},
	number = {3},
	year = {2009},
	month = {FEB},
	pages = {335-339},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A concise enantioselective synthesis of (S)-903, an inotropic agent, is described in nine linear steps and 95\% ee based on asymmetric dihydroxylation of cinnamate ester and Co-catalyzed Multifunctional reduction of several functional groups leading to the construction of core tetrahydroquinolin-3-ol, as the key steps. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2009.01.019},
	author = {Jagdale, Arun R. and Reddy, R. Santhosh and Sudalai, Arurnugam}
}
