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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/478

Title: An expeditious protocol for sesquiterpene-cored functionalized arenes from S-(-)-citronellal
Authors: Goel, Atul
Verma, Deepti
Keywords: Bisabolene
sesquiterpene
2H-pyran-2-ones
citronellal
ring transformation approach
Issue Date: 2009
Citation: Tetrahedron Lett (2009) 50, 2086-2089
Series/Report no.: CDRI Communication No. 7364
Abstract: An expeditious straightforward synthesis of sesquiterpene-cored arenes functionalized with electron-withdrawing or donating substituents is described and illustrated by Michael addition of S-(-)-citronellal on functionalized 2H-pyran-2-one in a single step at room temperature. The reaction was further generalized by synthesizing isoprenylated 9,10-dihydrophenanthrene-2-carbonitrile using 5,6-dihydro-2-oxo-4-sec-amino-2H-benzo[h]chromene-3-carbonitriles and S-(-)-citronellal under similar reaction conditions.
URI: http://hdl.handle.net/123456789/478
Appears in Collections:Medicinal and Process Chemistry

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