Recent progress in the synthesis of homotropane alkaloids adaline, euphococcinine and N-methyleuphococcinine
Lima, D. J. P., Santana, A. E. G., Birkett, Mike
and Porto, R. S.
(2021)
Recent progress in the synthesis of homotropane alkaloids adaline, euphococcinine and N-methyleuphococcinine.
Beilstein Journal of Organic Chemistry, 17.
pp. 28-41.
10.3762/bjoc.17.4
The 9-azabicyclo[3.3.1]nonane ring system is present in several insect- and plant-derived alkaloids. (−)-Adaline (1) and (+)-euphococcinine (2), found in secretions of Coccinelid beetles, and (+)-N-methyleuphococcinine (3), isolated from the Colorado blue spruce Picea pungens, are members of this alkaloid family. Their unique bicyclic system with a quaternary stereocenter, and the potent biological activity exerted by these homotropane alkaloids, make them attractive synthetic targets. This work aims briefly to review the chemical ecology of Adalia bipunctata and the recent methodologies to obtain adaline (1), euphococcinine (2), and N-methyleuphococcinine (3).
| Item Type | Article |
|---|---|
| Open Access | Gold |
| Keywords | 9-azabicyclo[3.3.1]nonane, Coccinelid beetles, Dipolar cycloaddition, Homotropane, Ring-closing metathesis |
| Project | BBSRC Strategic Programme in Smart Crop Protection |
| Date Deposited | 05 Dec 2025 10:27 |
| Last Modified | 19 Dec 2025 14:54 |
ORCID: https://orcid.org/0000-0002-3302-2025


