The synthesis of R-(+)- and S-(-)-isomers of substituted (E)- and (Z)-4(1H)-[1-(3-alkylamino-2-hydroxypropyl)-oximino]-2,3-dihydro-1,8-naphthyridine, in enantiomeric pure form, is described. These compounds showed an interesting beta-blocking activity. Generally, the (S)-enantiomers possess a slighthly higher affinity for beta receptors than the (R)-enantiomers.
Stereoselective synthesis and beta-blocking activity of substituted (E)- and (Z)- 4(1H) - [1- (3 - alkylamino - 2 - hydroxypropyl) oximino - 2,3 - dihydro - 1,8 - naphthyridine. Potential antihypertensive agents. Part VI
MANERA, CLEMENTINA;SACCOMANNI, GIUSEPPE;CALDERONE, VINCENZO;
1997-01-01
Abstract
The synthesis of R-(+)- and S-(-)-isomers of substituted (E)- and (Z)-4(1H)-[1-(3-alkylamino-2-hydroxypropyl)-oximino]-2,3-dihydro-1,8-naphthyridine, in enantiomeric pure form, is described. These compounds showed an interesting beta-blocking activity. Generally, the (S)-enantiomers possess a slighthly higher affinity for beta receptors than the (R)-enantiomers.File in questo prodotto:
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