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- Oxymercuration of 2-benzyl-2-azabicyclo[2.2.1]hept-5-en-3-one: explanation of stereoselectivity. Christopher F. Palmer, Ray McCague
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 2977
- Rearrangement of 2-azabicyclo[2.2.1]hept-5-en-3-ones: synthesis of cis-3-aminocyclopentane carboxylic acid derivatives. Christopher F. Palmer, Keith P. Parry, Stanley M. Roberts, Vladimir Sik
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 1021
- Synthesis of either enantiomer of cis-3-aminocyclopentanecarboxylic acid from both enantiomers of racemic 2-azabicyclo[2.2.1]hept-5-en-3-one. Chris Evans, Ray McCague, Stanley M. Roberts, Alan G. Sutherland
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 656
- Conversion of one enantiomer of the carbocyclic nucleoside synthon 2-azabicyclo[2.2.1]hept-5-en-3-one into the other. Christopher F. Palmer, Raymond McCague
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 1201
- Chemoenzymatic synthesis of (–)-carbovir utilizing a whole cell catalysed resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one. Steven J. C. Taylor, Alan G. Sutherland, Carol Lee, Richard Wisdom, Steve Thomas, Stanley M. Roberts, Christopher Evans
, J. Chem. Soc., Chem. Commun.
, 1990
, 1120
- Electrophilic substitution of a 2-azabicyclo[2.2.1]hept-5-en-3-one as a potential route to 3-deoxycarbocyclic nucleosides. Christopher F. Palmer, Keith P. Parry, Stanley M. Roberts
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 484
- 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
- Promiscuous enantioselective (−)-γ-lactamase activity in the Pseudomonas fluorescens esterase I. Leticia L. Torres, Anna Schließmann, Marlen Schmidt, Noella Silva-Martin, Juan A. Hermoso, José Berenguer, Uwe T. Bornscheuer, Aurelio Hidalgo
, Org. Biomol. Chem.
, 2012
, 10
, 3388
- 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
- Potential use of carbocyclic nucleosides for the treatment of AIDS: chemo-enzymatic syntheses of the enantiomers of carbovir. Chris T. Evans, Stanley M. Roberts, Karoline A. Shoberu, Alan G. Sutherland
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 589