@article { ISI:000347229500001,
	title = {One-pot quadruple/triple reaction sequence: a useful tool for the synthesis of natural products},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {13},
	number = {4},
	year = {2015},
	month = {OCT},
	pages = {970-973},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Multiple reactions in one pot has always been a useful technique for synthetic organic chemists, as it can minimizes solvent usage, time and the number of purification steps when compared to individual multi-step syntheses. In line with this, here in this perspective we discuss a one-pot quadruple/triple reaction sequence comprising an enyne ring-closing metathesis/cross-metathesis/Diels-Alder/aromatization for the synthesis of natural products setting.</p>},
	issn = {1477-0520},
	doi = {10.1039/c4ob02143f},
	author = {Kashinath, K. and Reddy, D. Srinivasa}
}
