Development of the biocatalytic resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one as an entry to single-enantiomer carbocyclic nucleosides

This publication has 10 references indexed in Scilit:

• Resolution of 4-amino-cyclopentanecarboxylic acid methyl esters using hydrolytic enzymes
  Enzyme and Microbial Technology, 1992
• Synthesis of chiral carbocyclic nucleosides
  Tetrahedron, 1992
• Synthèse des deux énantiomères de l'analogue carbocyclique du nicotinamide ribose et évaluation de leurs propriétés biologiques
  European Journal of Medicinal Chemistry, 1989
• Stereospecific synthesis of carbocyclic nucleosides from 2-azabicyclo-[2.2.1]heptan-3-ones via sodium borohydride mediated carbon-nitrogen bond cleavage
  Tetrahedron Letters, 1989
• Definition of subclasses of adenosine receptors associated with adenylate cyclase: interaction of adenosine analogs with inhibitory A₁ receptors and stimulatory A₂ receptors
  Canadian Journal of Physiology and Pharmacology, 1987
• Carbocyclic nucleosides
  Medicinal Research Reviews, 1986
• A mild two-step method for the hydrolysis of lactams and secondary amides
  The Journal of Organic Chemistry, 1983
• Quantitative analyses of biochemical kinetic resolutions of enantiomers
  Journal of the American Chemical Society, 1982
• Synthesis of carbocyclic aminonucleosides
  The Journal of Organic Chemistry, 1978
• Diels-Alder cycloadditions of sulfonyl cyanides with cyclopentadiene. Synthesis of 2-azabicyclo[2.2.1]hepta-2,5-dienes
  The Journal of Organic Chemistry, 1974