@article { ISI:000338109600007,
	title = {New enantioselective synthesis of the anti-parkinson agent safinamide},
	journal = {Synthesis-Stuttgart},
	volume = {46},
	number = {13},
	year = {2014},
	month = {JUL},
	pages = {1751-1756},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>An alternative highly enantioselective synthesis of the anti-Parkinson agent safinamide from simple, commercially available, starting materials is described. The protocol might also be useful in the synthesis of structural variants of safinamide, such as ralfinamide or related analogues</p>},
	keywords = {Amides, medicinal chemistry, safinamide, stereoselective synthesis},
	issn = {0039-7881},
	doi = {10.1055/s-0033-1341104},
	author = {Reddi, Anjaneyulu and Mujahid, Mohammad and Sasikumar, Murugesan and Muthukrishnan, Murugan}
}
@article {43499,
	title = {New and efficient enantioselective synthesis of both enantiomers of the calcium channel blocker bepridil},
	journal = {New Journal of Chemistry},
	volume = {41},
	year = {2017},
	month = {JAN},
	pages = {824-829},
	abstract = {A concise and efficient enantioselective synthesis of both enantiomers of bepridil, a calcium channel blocker, is reported. Jacobsen{\textquoteright}s hydrolytic kinetic resolution method was utilized to resolve racemic 2-(isobutoxymethyl) oxirane. The incorporation of the succinimide moiety by the Mitsunobu reaction, which was investigated in detail, occurred without any loss of enantioselectivity. Using this strategy, both enantiomers of the target molecule were obtained in good yield and with high enantiopurity (ee > 99\%).},
	doi = {10.1039/c6nj02928k},
	author = {Mujahid, Mohammad and Subramanian, Jambu and Nalla, Viswanadh and Sasikumar, Murugesan and Kunte, Sunita Sharad and Muthukrishnan, Murugan}
}
