Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/3464
Title: Enantiospecific total synthesis of ent-10,11-thapsan-10-ol
Authors: Srikrishna, A
Anebouselvy, K
Keywords: Enantiospecific
Thapsia garganica
thapsane
Thapsia villosa
Issue Date: 2009
Publisher: CSIR
Abstract: First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxythapsan-10-ol has been described. (R)-Carvone has been employed as the chiral starting material and a combination of intramolecular alkylation and Criegee fragmentation are employed for intramolecular stereospecific transfer of the chirality. An intramolecular diazoketone cyclopropanation and regioselective cyclopropane ring cleavage reactions have been employed for the creation of the three requisite contiguous quaternary carbon atoms.
Description: 413-422
URI: http://hdl.handle.net/123456789/3464
ISSN: 0376-4699
Appears in Collections:IJC-B Vol.48B(03) [March 2009]

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