@article { ISI:000227411400039,
	title = {Stereoselective synthesis of (-)-microcarpalide},
	journal = {Tetrahedron Letters},
	volume = {46},
	number = {11},
	year = {2005},
	month = {MAR},
	pages = {1939-1941},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A highly convergent and efficient synthesis of (-)-microcarpalide, a 10-membered lactone displaying remarkable microfilament disrupting activity is described. Ring-closing metathesis and Sharpless asymmetric dihydroxylations are the key steps. Our strategy highlights the application of novel hydroxy lactone precursors for the stereoselective synthesis of (-)-microcarpalide. (C) 2005 Elsevier Ltd. All rights reserved.</p>},
	keywords = {4-diol, cis-2-butene-1, Claisen ortho ester rearrangement, microcarpalide, Ring-closing metathesis, sharpless asymmetric dihydroxylation},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2005.01.052},
	author = {Chavan, Subhash P. and Praveen, C.}
}
@article { ISI:000351584500007,
	title = {Synthesis of 3-ethyl-4-metyl-1h,5-dihydro-2h-pyrrol-2-one by novel palladium(ii)-catalyzed cyclization and ring-closing metathesis},
	journal = {Synthesis-Stuttgart},
	volume = {47},
	number = {7},
	year = {2015},
	month = {APR},
	pages = {955-960},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Synthesis of 3-ethyl-4-methyl-1,5-dihydro-2H-pyrrol-2-one is described starting from commercially available allylamine and 4-methoxybenzylamine employing palladium-catalyzed cyclization or ring-closing metathesis as the key steps.</p>},
	keywords = {antidiabetic, cyclization, glimepiride, lactams, metabolite, pyrrolinone, Ring-closing metathesis},
	issn = {0039-7881},
	doi = {10.1055/s-0034-1379985},
	author = {Chavan, Subhash P. and Pathak, Ashok B. and Pawar, Kailash P.}
}
