@article { ISI:000359136500087,
	title = {Organocatalytic [4+1]-annulation approach for the synthesis of densely functionalized pyrazolidine carboxylates},
	journal = {RSC Advances},
	volume = {5},
	number = {80},
	year = {2015},
	month = {JUL},
	pages = {65554-65559},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A novel one-pot [4+1]-annulation process for the asymmetric synthesis of densely functionalized pyrazolidine carboxylates is described. The in situ generated gamma-hydrazino-alpha,beta-unsaturated ester obtained via proline catalysis acts as a four-atom component, and Corey{\textquoteright}s sulfur ylide or ethyl bromoacetate acts as a one-atom carbon source to construct pyrazolidine carboxylate units in a highly enantio- and diastereoselective fashion.</p>},
	issn = {2046-2069},
	doi = {10.1039/c5ra09583b},
	author = {Lalwani, Komal G. and Aher, Ravindra D. and Sudalai, Arumugam}
}
@article { ISI:000376695700026,
	title = {Organocatalytic route to enantioselective synthesis of ceramide trafficking inhibitor HPA-12},
	journal = {Tetrahedron Letters},
	volume = {57},
	number = {22},
	year = {2016},
	month = {JUN},
	pages = {2445-2447},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A new organocatalytic approach to the synthesis of ceramide trafficking inhibitor HPA-12 has been described starting from phenacyl bromide. The strategy involves chiral CBS reduction of gamma-ketoester and proline-catalyzed alpha-amination reaction of aldehyde followed by reduction as the key chirality inducing steps. (C) 2016 Elsevier Ltd. All rights reserved.</p>},
	keywords = {alpha-Amination, CBS reduction, Ceramide, Organocatalytic, Proline},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2016.04.087},
	author = {Lalwani, Komal G. and Sudalai, Arumugam}
}
