Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9095
Title: Enantiospecific synthesis of sesquiterpenes from (<i style="">R</i>)-carvone. Synthesis of 3-thapsenol
Authors: Srikrishna, A
Anebouselvy, K
Issue Date: May-2005
Publisher: CSIR
Series/Report no.: <b>Int</b>.<b>Cl</b>.<b><sup>7</sup> C 07 13/08</b>
Abstract: Enantiospecific synthesis of 3-thapsenol, comprising the carbon framework of a small group of sesquiterpenes containing three contiguous quaternary carbon atoms has been described. (<i style="">R</i>)-Carvone has been employed as the chiral starting material utilizing the isopropenyl group as a masked hydroxy group. A combination of alkylation, orthoester Claisen rearrangement and intramolecular diazo ketone cyclopropanation reactions has been employed for the creation of the three requisite contiguous quaternary carbon atoms.
Description: 1029-1039
URI: http://hdl.handle.net/123456789/9095
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(05) [May 2005]

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