Results
1 -
10 of
28
(Click
here to explore results)
- 6-Substituted 2-azabicyclo[2.2.1]hept-5-enes by nitrogen-directed radical rearrangement: synthesis of an epibatidine analogue with high binding affinity at the nicotinic acetylcholine receptor. David M. Hodgson, Christopher R. Maxwell, Richard Wisedale, Ian R. Matthews, Kate J. Carpenter, Anthony H. Dickenson, Susan Wonnacott
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 3150
- 2-Azanorbornane – a versatile chiral aza-Diels–Alder cycloadduct: preparation, applications in stereoselective synthesis and biological activity. Elżbieta Wojaczyńska, Jacek Wojaczyński, Karolina Kleniewska, Mateusz Dorsz, Tomasz K. Olszewski
, Org. Biomol. Chem.
, 2015
, 13
, 6116
- Construction of oxygenated 2-azabicyclo[2.2.1]heptanes via palladium-catalyzed 1,2-aminoacyloxylation of cyclopentenes. Haipin Zhou, Rui Pan, Menghua Xu, Jiao Ma, Aijun Lin, Hequan Yao
, Chem. Commun.
, 2023
, 59
, 3574
- Synthesis of epibatidine isomers: endo-5- and 6- (6′-chloro-3′-pyridyl-2-azabicyclo[2.2.1]heptanes. Caroline D. Cox, John R. Malpass, John Gordon, Alan Rosen
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 2372
- Meisenheimer rearrangements of N-allyl 2-azabornane derivatives. Jonathan E. H. Buston, Iain Coldham, Keith R. Mulholland
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 2327
- Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids. Ivo E. Sampaio-Dias, Sara C. Silva-Reis, Luís Pinto da Silva, Xerardo García-Mera, Miguel A. Maestro, José E. Rodríguez-Borges
, Org. Chem. Front.
, 2019
, 6
, 3540
- On the scope of oxidation of tertiary amines: Meisenheimer rearrangements versus Cope elimination in 2-(cyanoethyl)-2-azanorbornanes. Carlos A. D. Sousa, Ivo E. Sampaio-Dias, Xerardo García-Mera, Carlos F. R. A. C. Lima, José E. Rodríguez-Borges
, Org. Chem. Front.
, 2016
, 3
, 1624
- Synthetic studies toward longeracemine: a SmI2-mediated spirocyclization and rearrangement cascade to construct the 2-azabicyclo[2.2.1]heptane framework. Keita Komine, Kyle M. Lambert, Quentin R. Savage, Joshua B. Cox, John L. Wood
, Chem. Sci.
, 2020
, 11
, 9488
- Intramolecular functional group differentiation as a strategy for the synthesis of bridged bicyclic β-amino acids. Andriy V. Tymtsunik, Serhii O. Kokhan, Yevhen M. Ivon, Igor V. Komarov, Oleksandr O. Grygorenko
, RSC Adv.
, 2016
, 6
, 22737
- Measurement of nitrogen inversion barriers and invertomer ratios in constrained azabicyclic systems. John R. Malpass, Neil J. Tweddle
, J. Chem. Soc., Perkin Trans. 2
, 1978
, 120