@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:000243819800025,
	title = {Central core of uprolides D and E: a survey of some ring closing metathesis approaches},
	journal = {Tetrahedron Letter},
	volume = {48},
	number = {6},
	year = {2007},
	month = {FEB},
	pages = {1013-1016},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A preliminary study dealing with the feasibility of ring closing metathesis and ene-yne ring closing metathesis to construct the central bicyclic cores of uprolides D and E was investigated. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	keywords = {cembranolides, ene-yne metathesis, Ring closing metathesis, Sharpless asymmetric epoxidation, uprolides D and E},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.11.176},
	author = {Ramana, C. V. and Salian, Sumanth R. and Gurjar, Mukund K.}
}
