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Synthesis of 1-Substituted 5,5,8,8-Tetramethyl5,6,7,8-tetrahydronaphthalene-2,3-diols and 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalene-2,3-dione

Russian Journal of Organic Chemistry, 2020
A one-step procedure was developed for the multigram synthesis of 5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2,3-diol, and its three 1-substituted derivatives and 1-substituted 5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2,3-dione were obtained.
M. A. Zherebtsov   +3 more
openaire   +1 more source

Electrochemically Oxidative Polymerization of 1,2,3,4-Tetrahydronaphthalene

Bulletin of the Chemical Society of Japan, 1992
Abstract Electrochemical oxidation of 1,2,3,4-tetrahydronaphthalene (1) at higher anode potential than 3.0 V and high concentration of 1 gave a polymer of 1. The polymer deposited on an anode was slightly soluble in organic solvents and the polymer separated from the solution had number average molecular weight up to 1500.
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The dehydrobromination of 1,2‐dibromo‐1,2,3,4‐tetrahydronaphthalene

Recueil des Travaux Chimiques des Pays-Bas, 1965
AbstractDehydrobromination of 1,2‐dibromo‐1,2,3,4‐tetrahydronaphthalene with piperidine has been shown to give 1‐bromo‐3,4‐dihydronaphthalene.
A. G. M. Willems   +2 more
openaire   +1 more source

Modes of Methyleneoxy Bridging and Their Effect on Tetrahydronaphthalene Lignan Cytotoxicity

Journal of Medicinal Chemistry, 2003
Dioxatricyclodecane, oxabicyclooctane, and benzodihydropyran derivatives of alpha-conidendrin (ACON), podophyllotoxin (PT), and sikkimotoxin (SK) were prepared to learn which methyleneoxy bridging modes and arene and aryl substituents coincided with high cytotoxicity. PT-derived dioxatricyclodecane 14 showed in vitro activity at 10(-8) M.
Robert T, LaLonde   +4 more
openaire   +2 more sources

Electron Beam Irradiations of 1,2,3,4-Tetrahydronaphthalene

Radiation Research, 1965
Studies of radiation damage in model compounds can provide important knowledge for predicting the effects in more complex systems. This investigation of 1,2,3,4-tetrahydronaphthalene (tetralin) was part of a program of irradiating condensed-ring hydrocarbons selected to represent components of petroleum fuels and lubricants.
R. Y. Mixer   +4 more
openaire   +1 more source

ChemInform Abstract: CONTINUOUS PROCESS FOR TETRAHYDRONAPHTHALENE

Chemischer Informationsdienst, 1974
AbstractInstitut Francais du Petrole hat einen Übergangsmetallkatalysator für die selektive Hydrierung von Naphthalin zu hochreinem Tetrahydronaphthalin entwickelt.
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NEW ALKAMINES IN THE TETRAHYDRONAPHTHALENE SERIES

Journal of the American Chemical Society, 1931
Erich. Mosettig, Alfred. Burger
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