Conformationally restrained β-blocking oxime ethers: synthesis and β-adrenergic properties of diastereoisomeric anti and syn 2-(5′-isoxazolidinyl)-ethanolamines-Reference-Cited by-同舟云学术

Conformationally restrained β-blocking oxime ethers: synthesis and β-adrenergic properties of diastereoisomeric anti and syn 2-(5′-isoxazolidinyl)-ethanolamines

Published:1992-11 Issue:8 Volume:27 Page:751-764
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Balsamo A,Breschi MC,Chini M,Domiano P,Giannaccini G,Lucacchini A,Macchia B,Macchia M,Manera C,Martinelli A,Martini C,Martinotti E,Nieri P,Rossello A

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference38 articles.

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2. Role of the (acyloxy)methyl moiety in eliciting the adrenergic .beta.-blocking activity of 3-(acyloxy)propanolamines

3. Structure cristalline du (tert-butylamino-3 hydroxy-2 propoxyimino)-9 fluorène (IPS 339)

4. Chlorhydrate de chloro-4 acétophénone-O-(tert-butylamino-3 hydroxy-2 propyl)oxime (IPS 345)

5. Conformational effects on the activity of drugs. 4. Cyclic analogs of 1-(p-nitrophenyl)-2-isopropylaminoethanol. Synthesis and evaluation of the adrenergic .beta.-receptor blocking activity of 2-(p-nitrophenyl)-4-isopropylmorpholine

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