Enantioselective synthesis of hexahydrofuro[3,2-c] quinolines through a multicatalytic and multicomponent process. A new “aromatic sandwich” model for BINOL-phosphoric acid catalyzed reactions-Reference-Cited by-同舟云学术

Enantioselective synthesis of hexahydrofuro[3,2-c] quinolines through a multicatalytic and multicomponent process. A new “aromatic sandwich” model for BINOL-phosphoric acid catalyzed reactions

Published:2014 Issue:3 Volume:5 Page:996-1007
ISSN:2041-6520
Container-title:Chem. Sci.
language:en
Short-container-title:Chem. Sci.

Author:

Calleja Jonás,González-Pérez Adán B.,de Lera Ángel R.,Álvarez Rosana,Fañanás Francisco J.,Rodríguez Félix

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/SC/C3SC52891J

Reference92 articles.

1. Synthesis and Biological Evaluation of a New Series of Hexahydro-2H-pyrano[3,2-c]quinolines as Novel Selective σ1 Receptor Ligands

2. Highly efficient synthesis and characterization of the GPR30-selective agonist G-1 and related tetrahydroquinoline analogs

3. Structure–activity relationship (SAR) investigations of tetrahydroquinolines as BKCa agonists

4. Differential Antiviral Activity of Benzastatin C and Its Dechlorinated Derivative from Streptomyces nitrosporeus

5. Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1H-indol-3-yl)tetrahydroquinoline derivatives

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