Study of the Cis to Trans Isomerization of 1-Phenyl-2,3-disubstituted Tetrahydro-β-carbolines at C(1). Evidence for the Carbocation-Mediated Mechanism-Reference-Cited by-同舟云学术

Study of the Cis to Trans Isomerization of 1-Phenyl-2,3-disubstituted Tetrahydro-β-carbolines at C(1). Evidence for the Carbocation-Mediated Mechanism

Published:2009-03-10 Issue:7 Volume:74 Page:2771-2779
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kumpaty Hephzibah J.¹,Van Linn Michael L.¹,Kabir M. Shahjahan¹,Försterling F. Holger¹,Deschamps Jeffrey R.¹,Cook James M.¹

Affiliation:

1. Department of Chemistry, University of Wisconsin—Whitewater, Whitewater, Wisconsin 53190, Department of Chemistry and Biochemistry, University of Wisconsin—Milwaukee, Milwaukee, Wisconsin 53201, and Laboratory for the Structure of Matter, Naval Research Laboratory, Washington, D.C. 20375

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo8028168

Reference43 articles.

1. Über die Bildung von Isochinolin‐derivaten durch Einwirkung von Methylal auf Phenyl‐äthylamin, Phenyl‐alanin und Tyrosin

2. Über die Synthese von Carbolinderivaten

3. Solid-Phase Synthesis of 1-Substituted Tetrahydroisoquinoline Derivatives Employing BOC-Protected Tetrahydroisoquinoline Carboxylic Acids

4. The GABAAReceptor α1Subtype in the Ventral Pallidum Regulates Alcohol-Seeking Behaviors

5. GABAA and Opioid Receptors of the Central Nucleus of the Amygdala Selectively Regulate Ethanol-Maintained Behaviors

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