Studies towards the synthesis of FCRR toxin: an expeditious entry into 7-5-6 ring systems via [5+2] oxidopyrylium-alkene cycloaddition
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Title |
Studies towards the synthesis of FCRR toxin: an expeditious entry into 7-5-6 ring systems via [5+2] oxidopyrylium-alkene cycloaddition
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Creator |
KRISHNA, UM
TRIVEDI, GK |
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Subject |
-cycloaddition
3-oxidopyrylium derivatives strategy furans fcrr toxin indene [5+2] cycloaddition reductive cleavage |
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Description |
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
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Publisher |
PERGAMON-ELSEVIER SCIENCE LTD
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Date |
2011-08-26T17:30:31Z
2011-12-26T12:57:33Z 2011-12-27T05:43:06Z 2011-08-26T17:30:31Z 2011-12-26T12:57:33Z 2011-12-27T05:43:06Z 2004 |
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Type |
Article
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Identifier |
TETRAHEDRON LETTERS, 45(2), 257-259
0040-4039 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 |
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Language |
en
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