@article { ISI:000238012800020,
	title = {Synthetic studies toward macrocidins: an RCM approach for the construction of the central cyclic core},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {24},
	year = {2006},
	month = {JUN},
	pages = {4061-4064},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The central macrocyclic core of the macrocidins was constructed using RCM as the key reaction. A preliminary investigation dealing with the key reactions, that is, the Dieckmann cyclization and the RCM, revealed that RCM of the beta-ketoamide is better than RCM of the corresponding acyltetramic acid. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	keywords = {acyltetramic acid, Lacey-Dieckmann cyclization, macrocidins, Ring closing metathesis},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.03.192},
	author = {Ramana, C. V. and Mondal, Mohabul A. and Puranik, Vedavati G. and Gurjar, Mukund K.}
}
@article { ISI:000303429600017,
	title = {Formal synthesis of (-)-stemoamide using a useful epimerization at C-8},
	journal = {Tetrahedron Letters},
	volume = {53},
	number = {21},
	year = {2012},
	month = {MAY},
	pages = {2647-2650},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The formal synthesis of (-)-stemoamide was achieved starting from L-pyroglutamic acid. The key steps used are the allylation using BF3 center dot OEt2, ring closing metathesis, allylic oxidation and a novel epimerization at C8. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Allylation, Allylic oxidation, Pyroglutamic acid, Ring closing metathesis, Stemoamide},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2012.03.054},
	author = {Chavan, Subhash P. and Harale, Kishor R. and Puranik, Vedavati G. and Gawade, Rupesh L.}
}
