Preparation of the (R) and (S) enantiomers of 10-hydroxymethylfuro[3,4-c]-β-carboline-2(10H)one, the first example of a benzodiazepine receptor ligand of the β-carboline family having a stereogenic center-Reference-Cited by-同舟云学术

Preparation of the (R) and (S) enantiomers of 10-hydroxymethylfuro[3,4-c]-β-carboline-2(10H)one, the first example of a benzodiazepine receptor ligand of the β-carboline family having a stereogenic center

Published:1995-02 Issue:2 Volume:6 Page:455-462
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Dubois Laurent,Dorey Gilbert,Potier Pierre,Dodd Robert H

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference12 articles.

1. Dorey, G.; Dubois, L.; Prado de Carvalho, L.; Potier, P.; Dodd, R.H. J. Med. Chem. in press

2. The rapidly expanding range of neuronal benzodiazepine receptor ligands

3. Synthesis and benzodiazepine receptor affinities of rigid analogs of 3-carboxy-.beta.-carbolines: demonstration that the benzodiazepine receptor recognizes preferentially the s-cis conformation of the 3-carboxy group

4. Benzodiazepine Receptor: Demonstration in the Central Nervous System

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