Stereoselectivity at ?-adrenoreceptor subtypes: observations with the enantiomers of WB 4101 separated through their amides ofN-Tosyl-(S)-proline-Reference-Cited by-同舟云学术

Stereoselectivity at ?-adrenoreceptor subtypes: observations with the enantiomers of WB 4101 separated through their amides ofN-Tosyl-(S)-proline

Published:1992 Issue:1 Volume:4 Page:16-20
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Andrisano Vincenza,Marucci Gabriella,Melchiorre Carlo,Tumiatti Vincenzo

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference14 articles.

1. The α-adrenoceptor blocking effects of a new benzodioxane

2. See review: Recent developments in structure-activity relationships among inhibitors of the adrenergic ?-receptor. In: Adrenoceptors and Catecholamine Action. Part A: ed. New York: John Wiley, 1981: 181-211.

3. See review: Direct binding studies of ?-adrenoceptors. In: Adrenoceptors and Catecholamine Action. Part A: ed. New York: John Wiley, 1981: 131-179.

4. Absolute configuration of glycerol derivatives. 6. Cupra A circular dichroism spectra of 3-(aryloxy)-1-(alkylamino)-2-propanol. .beta.-Adrenergic blocking agents

5. Absolute configuration of glycerol derivatives. 7. Enantiomers of 2-[[[2-(2,6-dimethoxyphenoxy)ethyl]amino]ethyl]-1,4-benzodioxane (WB-4101), a potent competitive .alpha.-adrenergic antagonist

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