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cotarnine

Known as: 1,3-Dioxolo(4,5-g)isoquinolin-5-ol, 5,6,7,8-tetrahydro-4-methoxy-6-methyl- (9CI), 5,6,7,8-tetrahydro-4-methoxy-6-methyl-1,3- dioxolo(4,5-g)isoquinolin-5-ol, 5,6,7,8-Tetrahydro-4-methoxy-6-methyl-1,3-dioxolo(4,5-g)isoquinolin-5-ol 
 
National Institutes of Health

Papers overview

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2016
2016
C(sp)-H Bond activation of acetylene molecule still remains a challenge for synthetic organic chemists. In practice, acetylenes… Expand
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2009
2009
A sensitive, selective, precise and stability-indicating thin-layer chromatographic (TLC) method was developed and validated for… Expand
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2008
2008
Cotarnine was reacted with barbituric acid and its N-alkylbartituric and 1,3-dimethyl-2-thio analogs under forcing conditions to… Expand
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2005
2005
Abstract1-Substituted 1,2,3,4-tetrahydroisoquinoline systems were prepared by reaction of cotarnine with the NH-and CH-acids… Expand
2004
2004
Chlorinated cotarnine was alkynated in the 1-position upon brief heating in acetonitrile with silver acetylenides of… Expand
2004
2004
The reaction of barbituric acid and its N-substituted derivatives and 2-thio analogs with cotarnine forms 5-(4-methoxy-6-methyl-5… Expand
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1988
1988
Noscapine, narcotoline and cotarnine were quantified in deproteinized plasma samples by using a coupled-column liquid… Expand
1979
1979
1. The metabolism of noscapine was studied in rabbits, rats and human. 2. Apart from the O-demethylated metabolites already… Expand
1954
1954
For testing compounds for antitussive activity, methods are described which give linear dose-response relationships. It was found… Expand
1939
1939
ALTHOUGH it is now many years since myristicin was first isolated from the oils of nutmeg and mace, its synthesis has not… Expand