@article { ISI:000248238400001,
	title = {Application of hydrolytic kinetic resolution (HKR) in the synthesis of bioactive compounds},
	journal = {Tetrahedron},
	volume = {63},
	number = {13},
	year = {2007},
	month = {MAR},
	pages = {2745-2785},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	keywords = {Biological activity, bis-epoxides, Hydrolytic kinetic resolution, meso-epoxides, Natural products, synthesis, terminal epoxides},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2006.12.015},
	author = {Kumar, Pradeep and Naidu, Vasudeva and Gupta, Priti}
}
@article { ISI:000267168600002,
	title = {Hydrolytic kinetic resolution as an emerging tool in the synthesis of bioactive molecules},
	journal = {Synlett},
	number = {9},
	year = {2009},
	month = {JUN},
	pages = {1367-1382},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A variety of racemic epoxides mainly derived from terminal olefins, such as aliphatic epoxides, multifuncitonalized epoxides and amine-substituted epoxides, have been successfully resolved into the enantiomerically pure epoxides and diols using Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR) method. The chiral epoxides thus prepared were further elaborated by synthetic manipulation to provide a variety Of Compounds of biological interest. A general synthetic strategy for the construction Of S synlanti-1,3-polyol systems using iterative HKR has been developed, which was subsequently utilized in the synthesis of natural products with a broad range of biological activity. The protocol for the 1,3-polyols was also further extended to the synthesis of 1,3-amino alcohols.</p>},
	keywords = {Biological activity, Hydrolytic kinetic resolution, Natural products, synthesis, terminal epoxides},
	issn = {0936-5214},
	doi = {10.1055/s-0029-1217171},
	author = {Kumar, Pradeep and Gupta, Priti}
}
@article { ISI:000285311000016,
	title = {Enantio- and diastereocontrolled total synthesis of (+)-strictifolione},
	journal = {European Journal of Organic Chemistry},
	number = {36},
	year = {2010},
	month = {DEC},
	pages = {6993-7004},
	publisher = {WILEY-BLACKWELL},
	address = {COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA},
	abstract = {<p>A concise and practical enantioselective synthesis of (+)-strictifolione has been achieved in high diastereomeric excess using Jacobsen{\textquoteright}s hydrolytic kinetic resolution, proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons olefination of aldehyde and cross olefin/ring-closing metathesis as the key steps.</p>},
	keywords = {Asymmetric synthesis, Hydrolytic kinetic resolution, lactones, Natural products, organocatalysis, Ring-closing metathesis, Total synthesis},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201001221},
	author = {Kumar, Pradeep and Pandey, Menaka and Gupta, Priti and Naidu, S. Vasudeva and Dhavale, Dilip D.}
}
