Author/Authors :
Jagtap، نويسنده , , Prakash G. and Chen، نويسنده , , Zhiyu and Koppetsch، نويسنده , , Karsten and Piro، نويسنده , , Elizabeth and Fronce، نويسنده , , Paula and Southan، نويسنده , , Garry J. and Klotz، نويسنده , , Karl-Norbert Klotz، نويسنده ,
Abstract :
Synthesis of potent adenosine A2A and A3 receptor agonist from the modification of adenosine-5′-N-ethylcarboxamide (NECA) has been reported. Diastereoisomer possessing an (R)-3,4-dihydro-2H-pyranyl (DHP) moiety exhibited the highest affinity at the A2A and A3 receptors. The key steps involve the synthesis of (R)-3,4-dihydro-2H-pyran-2-carboxaldehyde (7), which was obtained through the enzyme-catalyzed kinetic resolution of (±)-2-acetoxymethyl-3,4-dihydro-2H-pyran (5).
