@article { ISI:000260756600004,
	title = {Carbohydrate templates for the synthesis of prototype renin inhibitors},
	journal = {Tetrahedron-Asymmetry},
	volume = {19},
	number = {18},
	year = {2008},
	month = {SEP},
	pages = {2123-2129},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A concise synthesis of a prototype renin inhibitor and its 7-epimer has been accomplished starting from readily available D-glucose. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2008.08.007},
	author = {Mohapatra, Debendra K. and Sahoo, Gokarneswar and Sankar, Kuppusamy and Gurjar, Mukund K.}
}
@article { ISI:000300339800033,
	title = {Practical syntheses of proposed and revised manzacidin B and their congeners},
	journal = {Organic Letters},
	volume = {14},
	number = {4},
	year = {2012},
	month = {FEB},
	pages = {1082-1085},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A concise and highly stereoselective total synthesis of manzacidin B and its congeners has been developed following chelation-controlled syn-epoxidation and Lewis acid catalyzed intramolecular regioselective epoxide ring opening to generate the quarternary amine center. Elaboration of the triol moiety to the target molecule was achieved in good overall yield, representing practical total syntheses of manzacidin B and its congeners. From the XRD, NMR, and analytical data, the correct structure of natural manzacidin B, (4R,5R,6R)-6, was confirmed.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol203466m},
	author = {Sankar, Kuppusamy and Rahman, Hasibur and Das, Pragna P. and Bhimireddy, Eswar and Sridhar, B. and Mohapatra, Debendra K.}
}
