Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/xmlui/handle/10054/11388
Title: Studies towards the synthesis of FCRR toxin: an expeditious entry into 7-5-6 ring systems via [5+2] oxidopyrylium-alkene cycloaddition
Authors: KRISHNA, UM
TRIVEDI, GK
Keywords: <5+2>-Cycloaddition
3-Oxidopyrylium
Derivatives
Strategy
Furans
Issue Date: 2004
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Citation: TETRAHEDRON LETTERS, 45(2), 257-259
Abstract: Synthetic studies towards the diterpene natural product FCRR toxin have been undertaken. Ail intermolecular [5+2] oxidopyrylium-alkene cycloaddition reaction was employed to construct the 7-5-6 tricyclic framework. The reaction proceeded with very high regio- and stereoselectivity and the bridging ether was reductively cleaved to unmask the carbocycle. (C) 2003
URI: http://dx.doi.org/10.1016/j.tetlet.2003.10.185
http://dspace.library.iitb.ac.in/xmlui/handle/10054/11388
http://hdl.handle.net/10054/11388
ISSN: 0040-4039
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