Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.

Issue 22, 1997
Previous Article Next Article

Enantiospecific total synthesis of (+)-2-pupukeanone


The first total synthesis of chiral 2-pupukeanone (+)-4, starting from R-carvone (–)-7 employing a 5-exo-trig radical cyclisation as the key reaction for the construction of the tricyclic isotwistane carbon framework, is described.

Back to tab navigation

Article information

J. Chem. Soc., Perkin Trans. 1, 1997, 3293-3294
Article type

Enantiospecific total synthesis of (+)-2-pupukeanone

A. Srikrishna and T. Jagadeeswar Reddy, J. Chem. Soc., Perkin Trans. 1, 1997, 3293
DOI: 10.1039/A706321K

Search articles by author