@article { ISI:000360112400004,
	title = {Concise synthesis of (+/-)-clopidogrel via carboxylation of benzylamine with CO2},
	journal = {Synthetic Communications},
	volume = {45},
	number = {18},
	year = {2015},
	month = {JUN},
	pages = {2099-2105},
	publisher = {TAYLOR \& FRANCIS INC},
	address = {530 WALNUT STREET, STE 850, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>A concise and efficient synthesis of (+/-)-clopidogrel, an antithrombotic agent, is achieved by inserting CO2 at the benzylic position as the key reaction without using any toxic transition metals. The overall yield of the synthetic process is 38\% and the salient features include operationally simple process chemistry and fewer steps.</p>},
	keywords = {Antithrombatic agent, clopidogrel, CO2 insertion, Plavix},
	issn = {0039-7911},
	doi = {10.1080/00397911.2015.1061671},
	author = {Venkataramasubramanian, V. and Sudalai, Arumugam}
}
@article { ISI:000373408800021,
	title = {Concise enantioselective synthesis of (+)-sertraline and (-)-CP-52002 using proline catalysis},
	journal = {Tetrahedron Letters},
	volume = {57},
	number = {9},
	year = {2016},
	month = {MAR},
	pages = {1053-1055},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short enantioselective synthesis of (+)-sertraline and its C-4 epimer (-)-CP-52002 with an overall yield of 30\%, respectively, as its hydrochloride has been described. The key steps are the proline catalyzed Mannich reaction of acetaldehyde and acid catalyzed intramolecular Friedel-Crafts{\textquoteright} alkylation reaction of olefin proceeding with high optical purities. (C) 2016 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Indatraline, Mannich reaction, Proline catalysis, Sertraline, Tametraline},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2016.01.085},
	author = {Kalshetti, Rupali G. and Venkataramasubramanian, V. and Kamble, Sanjay P. and Sudalai, Arumugam}
}
