@article { ISI:000336700700003,
	title = {New enantioselective synthesis of (S)-2-ethoxy-3-(4-hydroxyphenyl)Propanoic acid esters (EEHP and IEHP), useful pharmaceutical intermediates of PPAR agonists},
	journal = {Tetrahedron Letters},
	volume = {55},
	number = {21},
	year = {2014},
	month = {MAY},
	pages = {3223-3226},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A new enantioselective synthetic route to the title compounds has been developed in a simple and practical way with high enantiopurity using commercially available starting material. (C) 2014 Elsevier Ltd. All rights reserved.</p>},
	keywords = {EEHP, Epoxide, IEHP, PPAR agonists},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2014.04.021},
	author = {Mujahid, Mohammad and Kunte, S. S. and Muthukrishnan, Murugan}
}
@article {48909,
	title = {Efficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine},
	journal = {Arkivoc},
	year = {2023},
	month = {JUL},
	type = {Article},
	abstract = {<p>An efficient synthesis of a well known chiral herbicide, (S)-metolachlor has been described using 2methoxymethylaziridine ring formation and reductive ring opening as key steps using commercially available (R)-epichlorohydrin. The present protocol delivers the required enantiomer of metolachlor in overall yield of 50.8\% and high enantiopurity (\&gt;99\%).</p>
},
	keywords = {Aziridine, Epoxide, Epoxide ring opening, herbicide synthesis, Metolachlor},
	issn = {1551-7004},
	doi = {10.24820/ark.5550190.p011.954},
	author = {Nalla, Viswanadh and Mujahid, Mohammad and Sasikumar, Murugesan and Mujumdar, Prashant and Muthukrishnan, Murugan}
}
