@article { ISI:000242639200001,
	title = {Evolution of the stereoselective pinacol coupling reaction},
	journal = {Tetrahedron},
	volume = {62},
	number = {52},
	year = {2006},
	month = {DEC},
	pages = {12137-12158},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	keywords = {diastereoselective, enantioselective., pinacol coupling, reductive dimerization},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2006.09.002},
	author = {Chatterjee, A. and Joshi, Navalkishore N.}
}
@article { ISI:000379437100016,
	title = {Formal enantioselective synthesis of (-)-epiquinamide by proline-catalyzed one-pot sequential -amination/propargylation of aldehyde and asymmetric dihydroxylation of olefin},
	journal = {Synlett},
	volume = {27},
	number = {11},
	year = {2016},
	month = {JUL},
	pages = {1699-1702},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Two independent routes to the formal synthesis of (-)-epiquinamide, have been described: the first route utilizes an l-proline-catalyzed one-pot sequential -amination/propargylation of aldehyde, while the second one employs asymmetric dihydroxylation as the key reaction to install the stereochemistry. While the first synthesis was accomplished in nine steps with 24.4\% overall yield and dr 9:1, the second strategy resulted in the synthesis in eight steps with 36.4\% overall yield and with perfect enantiocontrol.</p>},
	keywords = {Amination, diastereoselective, Dihydroxylation, Proline, quinolizidine},
	issn = {0936-5214},
	doi = {10.1055/s-0035-1561956},
	author = {Ahuja, Brij Bhushan and Emmanuvel, Lourdusamy and Sudalai, Arumugam}
}
