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Tetrahydronaphthalenes

Known as: Tetrahydronaphthalenes [Chemical/Ingredient], Tetralins 
Partially saturated 1,2,3,4-tetrahydronaphthalene compounds.
National Institutes of Health

Papers overview

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Highly Cited
2017
Highly Cited
2017
Hybrid catalyst systems to achieve acceptorless dehydrogenation of N-heterocycles and tetrahydronaphthalenes-model substrates for… Expand
  • table 1
  • figure 2
Highly Cited
2014
Highly Cited
2014
Reactions of amino, aminomethyl tetralins and benzyl alcohol with chlorosulphonyl isocyanate (CSI) afforded sulphamoyl carbamates… Expand
Review
2012
Review
2012
  • S. Gibbons
  • Clinical toxicology
  • 2012
  • Corpus ID: 4009570
Introduction. ‘Legal highs’ are psychoactive chemicals which are sold from ‘head shops’, the internet and from street suppliers… Expand
Review
2012
Review
2012
Background: Recreational use of designer substances containing synthetic cathinones such as mephedrone, commonly sold as “bath… Expand
Review
2008
Review
2008
Palladium-catalyzed transformations of aryl halides and pseudo-halides involving carbonylation, carbon-carbon and carbon… Expand
  • table 1
2008
2008
Previously, comprehensive two-dimensional gas chromatography-time of flight-mass-spectrometry (GCxGC-ToF-MS) revealed that the… Expand
Highly Cited
2007
Highly Cited
2007
Comprehensive two-dimensional gas chromatography-time-of-flight-mass-spectrometry can be used to resolve and identify individual… Expand
Highly Cited
2004
Highly Cited
2004
[reaction: see text] We herein report that RuCl(3)/AgOTf has proven to be a hydroarylation catalyst with an efficiency and scope… Expand
Highly Cited
1983
Highly Cited
1983
Musk xylene and musk ketone (synthetic musks) were detected in 100% and 80%, respectively of 74 samples, [freshwater fish (three… Expand
  • figure 1
Highly Cited
1969
Highly Cited
1969
Nucleophilic acylation is the attachment of an group to an electrophilic center. A brief discussion of the advantages offered… Expand
  • table 1