@article { ISI:000263299000005,
	title = {Asymmetric synthesis of tetrahydroquinolin-3-ols via CoCl2-catalyzed reductive cyclization of nitro cyclic sulfites with NaBH4},
	journal = {Organic Letters},
	volume = {11},
	number = {4},
	year = {2009},
	month = {FEB},
	pages = {803-806},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A new method for the construction of chiral 3-substituted tetrahydroquinoline derivatives based on asymmetric dihydroxylation and CoCl2-catalyzed reductive, cyclization of nitro cyclic sulfites with NaBH4 has been described with high optical purities. This method has been successfully applied in the formal synthesis of PNU 95666E and anachelin H chromophore.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol8028109},
	author = {Jagdale, Arun R. and Reddy, R. Santhosh and Sudalai, Arumugam}
}
@article { ISI:000312607100004,
	title = {Asymmetric synthesis of (+)-stagonolide C and (-)-aspinolide A via organocatalysis},
	journal = {Tetrahedron-Asymmetry},
	volume = {23},
	number = {22-23},
	year = {2012},
	month = {DEC},
	pages = {1534-1541},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A new enantioselective synthesis of two important fungal metabolites, (+)-stagonolide C and (-)-aspinolide A, has been described from readily available raw materials. Praline catalyzed asymmetric alpha-aminooxylation and Jorgensen{\textquoteright}s epoxidation of aldehydes are the key reactions employed in the introduction of chirality. The formation of the 10-membered lactone core structure was finally accomplished via Steglich esterification and ring closing metathesis reactions. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2012.10.007},
	author = {Shelke, Anil M. and Rawat, Varun and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
