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IJC-B Vol.49B [2010] >
IJC-B Vol.49B(06) [June 2010] >


Title: Enantiospecific total synthesis of ent-5-senecioyloxy-10,11-epoxythapsan-10-ol
Authors: Srikrishna, A
Anebouselvy, K
Keywords: Thapsia
thapsane
sesquiterpene
enantiospecific
Issue Date: Jun-2010
Publisher: CSIR
Abstract: Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,11-epoxythapsan-10-ol has been described. (R)-Carvone has been employed as the chiral starting material and a combination of intramolecular alkyation 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.
Page(s): 776-788
Source:IJC-B Vol.49B(06) [June 2010]

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