Asymmetric Synthesis of Enantiomerically Pure 2-Substituted Tetrahydro-3-benzazepines and Their Affinity to σ1 Receptors-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Enantiomerically Pure 2-Substituted Tetrahydro-3-benzazepines and Their Affinity to σ1 Receptors

Published:2009-03-06 Issue:7 Volume:74 Page:2788-2793
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Husain Syed Masood¹,Fröhlich Roland¹,Schepmann Dirk¹,Wünsch Bernhard¹

Affiliation:

1. Institut für Pharmazeutische and Medizinische Chemie der Westfälischen Wilhelms-Universität Münster, Hittorfstrasse 58-62, D-48149 Münster, Germany, and Organisch-Chemisches Institut der Westfälischen Wilhelms-Universität Münster, Corrensstr. 40, D-48149 Münster, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900087e

Reference26 articles.

1. Chemistry and biological activity of new 3-benzazepines

2. Comparison of balanol from Verticillium balanoides and ophiocordin from Cordyceps ophioglossoides.

3. Synthesis and dopaminergic binding of 2-aryldopamine analogs: phenethylamines, 3-benzazepines, and 9-(aminomethyl)fluorenes

4. Fenoldopam: A New Dopamine Agonist for the Treatment of Hypertensive Urgencies and Emergencies

5. Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity

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