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cyclopropylbenzene

Known as: Benzene, cyclopropyl- 
 
National Institutes of Health

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Broader (1)

Benzene Derivatives

Papers overview

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2016
2016
Metal Nanoparticles Catalyzed Selective Carbon-Carbon Bond Activation in the Liquid Phase.
Understanding the C-C bond activation mechanism is essential for developing the selective production of hydrocarbons in the… Expand
2005
2005
Quantitative Generalization of Solvent Effect on Radical Halogenation of Hydrocarbons
The dependences of the isomer ratio in photochemical chlorination of 2,3-dimethylbutane and of the selectivity in photochemical… Expand
  • table 1
2004
2004
Catechols of novel substrates produced using the toluene ring oxidation pathway of Pseudomonas sp. strain T-12
SummaryPseudomonas sp. strain T-12 transforms several substituted benzenes to catechols utilizing the two initial enzymes of the… Expand
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Highly Cited
2001
Highly Cited
2001
In vitro inhibition of cytochrome P450 enzymes in human liver microsomes by a potent CYP2A6 inhibitor, trans-2-phenylcyclopropylamine (tranylcypromine), and its nonamine analog, cyclopropylbenzene.
Currently, there are no selective, well characterized inhibitors for CYP2A6. Therefore, the effects of trans-(+/-)-2… Expand
2001
2001
Molecular structure and conformation of cyclopropylbenzene as determined by ab initio molecular orbital calculations, pulsed-jet fourier transform microwave spectroscopic, and gas-phase electron…
Ab initio computational, microwave spectroscopic, and electron diffraction techniques have been used to study the gas-phase… Expand
2001
2001
Substrate Specificity of Soluble Methane Monooxygenase
ion or by sequential loss of a *-bond electron and a proton termed an aborted epoxidation by Ortiz de Montellano (1986) and… Expand
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2001
2001
IN VITRO INHIBITION OF CYTOCHROME P 450 ENZYMES IN HUMAN LIVER MICROSOMES BY A POTENT CYP 2 A 6 INHIBITOR , TRANS-2-PHENYLCYCLOPROPYLAMINE ( TRANYLCYPROMINE ) , AND ITS NONAMINE ANALOG
Currently, there are no selective, well characterized inhibitors for CYP2A6. Therefore, the effects of trans-(6)-2… Expand
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1994
1994
Electron transfer in P450 mechanisms. Microsomal metabolism of cyclopropylbenzene and p-cyclopropylanisole.
  • P. Riley, R. Hanzlik
  • Xenobiotica; the fate of foreign compounds in…
  • 1994
    • Corpus ID: 32579826
1. The metabolism of cyclopropylbenzene (1a) and 4-cyclopropylanisole (1b) was studied using liver microsomal preparations from… Expand
1985
1985
Oxidation of arylcyclopropanes by rabbit liver cytochrome P-450. Mechanistic implications of a multiple oxidation.
The arylcyclopropanes (cyclopropylarenes) cyclopropylbenzene and diphenylcyclopropane are oxidized by rabbit liver microsomal… Expand
1982
1982
The oxidation of cyclopropyl benzene by rat liver microsomal cytochrome P‐450: an unusual triple oxidation of a substrate
The mechanism of hydroxylation of both aliphatic and aromatic molecules by cytochromes P450 and related chemical model systems… Expand
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