@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.}
}
@article { ISI:000251275500002,
	title = {Expeditious assembly of 3,4-benzannulated 8-oxabicyclo[3.2.1]octane systems by [2+2+2] alkyne cyclotrimerisation: Total synthesis of (-)-bruguierol A},
	journal = {European Journal of Organic Chemistry},
	number = {33},
	year = {2007},
	month = {NOV},
	pages = {5483-5486},
	publisher = {WILEY-V C H VERLAG GMBH},
	type = {Article},
	address = {PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY},
	abstract = {<p>Facile construction of benzene-fused 8-oxabicyclo[3.2.1]octane systems by employing a cross alkyne cyclotrimerisation reaction was explored. With this procedure, (-)-bruguierol A was synthesised, and its absolute configuration was established.</p>},
	keywords = {cyclotrimerisation, epoxidation, Total synthesis, Wilkinson{\textquoteright}s catalyst},
	issn = {1434-193X},
	doi = {10.1002/ejoc.200700648},
	author = {Ramana, Chepuri V. and Salian, Sumanth R. and Gonnade, Rajesh G.}
}
