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6'-hydroxycinchonidine

Known as: cupreidine 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Quinine
analogs & derivatives

Papers overview

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2018
2018
Enantioselective Conjugate Additions of 2-Alkoxycarbonyl-3(2 H)-furanones.
Enantioselective conjugate additions of in situ generated 2-alkoxycarbonyl-3(2 H)-furanones to three distinct types of… 
2012
2012
Excited-state proton transfer and ion pair formation in a Cinchona organocatalyst.
The excited-state proton transfer and subsequent intramolecular ion pair formation of a cupreidine-derived Cinchona… 
Highly Cited
2010
Highly Cited
2010
Asymmetric addition of indoles to isatins catalysed by bifunctional modified cinchona alkaloid catalysts.
The development of new and more efficient catalytic reactions is of paramount importance, particularly for the synthesis of… 
Highly Cited
2010
Highly Cited
2010
Catalytic asymmetric domino Michael-Henry reaction: enantioselective access to bicycles with consecutive quaternary centers by using bifunctional catalysts.
The use of domino and cascade reactions provides a powerful tool in organic synthetic chemistry. The possibility of forming… 
2010
2010
Excited state proton transfer in the Cinchona alkaloid cupreidine.
Photophysical properties of the organocatalyst cupreidine (CPD) and its chromophoric building block 6-hydroxyquinoline (6HQ) in… 
1982
1982
Hemodynamic Properties of a New Quinidine Analog, Cupreidine (6'‐Hydroxycinchonine)
Summary Cupreidine (6'-hydroxycinchonine) is a recently synthesized analog of quinidine (6'-methoxycinchonine). Previous studies… 
1981
1981
Identification of new urinary metabolites in man of quinine using methane chemical ionization gas chromatography-mass spectrometry.
1. Six new metabolites of quinine have been identified in urine of man by methane chemical ionization g.l.c.--mass spectrometry… 
1980
1980
A comparative study on the antiarrhythmic activity and acute toxicity of quinidine and four new analogs in mice.
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