BIOMAT Database Logo BIOMAT Database Logo

[Varions 2-aminomethylated nucleus-substituted indanones-(1)]. 1973

E Hannig, and R Heyde, and H Matschiner

UI MeSH Term Description Entries
D007192 Indenes A family of fused-ring hydrocarbons isolated from coal tar that act as intermediates in various chemical reactions and are used in the production of coumarone-indene resins.
D007659 Ketones Organic compounds containing a carbonyl group Ketone
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D011048 Polarography An electrochemical technique for measuring the current that flows in solution as a function of an applied voltage. The observed polarographic wave, resulting from the electrochemical response, depends on the way voltage is applied (linear sweep or differential pulse) and the type of electrode used. Usually a mercury drop electrode is used. DC Polarography,Pulse Polarography,Polarography, DC,Polarography, Pulse
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D004355 Drug Stability The chemical and physical integrity of a pharmaceutical product. Drug Shelf Life,Drugs Shelf Lives,Shelf Life, Drugs,Drug Stabilities,Drugs Shelf Life,Drugs Shelf Live,Life, Drugs Shelf,Shelf Life, Drug,Shelf Live, Drugs,Shelf Lives, Drugs
D006863 Hydrogen-Ion Concentration The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH pH,Concentration, Hydrogen-Ion,Concentrations, Hydrogen-Ion,Hydrogen Ion Concentration,Hydrogen-Ion Concentrations
D000586 Amination The creation of an amine. It can be produced by the addition of an amino group to an organic compound or reduction of a nitro group. Aminations
D000935 Antifungal Agents Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. Anti-Fungal Agents,Antifungal Agent,Fungicides, Therapeutic,Antibiotics, Antifungal,Therapeutic Fungicides,Agent, Antifungal,Anti Fungal Agents,Antifungal Antibiotics
D012996 Solutions The homogeneous mixtures formed by the mixing of a solid, liquid, or gaseous substance (solute) with a liquid (the solvent), from which the dissolved substances can be recovered by physical processes. (From Grant & Hackh's Chemical Dictionary, 5th ed) Solution

Related Publications

E Hannig, and R Heyde, and H Matschiner
Microwave-assisted synthesis of highly substituted aminomethylated 2-pyridones.
November 2004, The Journal of organic chemistry,
E Hannig, and R Heyde, and H Matschiner
Chemotherapeutic nitroheterocycles. 18. 2-(5-Nitro-2-imidazolylmethylene)-1-indanones, -1-tetralones, and -acetophenones substituted by aminoalkoxy groups.
March 1975, Journal of medicinal chemistry,
E Hannig, and R Heyde, and H Matschiner
Enantioselective synthesis of substituted indanones from silyloxyallenes.
February 2010, Journal of the American Chemical Society,
E Hannig, and R Heyde, and H Matschiner
2-Alkyll-indanones.
December 1948, Journal of the American Chemical Society,
E Hannig, and R Heyde, and H Matschiner
[1,3-Dicarbonyl compounds, 5. Enolacetates of 2-acyl-1-indanones].
May 1975, Archiv der Pharmazie,
E Hannig, and R Heyde, and H Matschiner
Molecular modifications of 2-arylidene-1-indanones leading to increased cytotoxic potencies.
February 2007, Journal of enzyme inhibition and medicinal chemistry,
E Hannig, and R Heyde, and H Matschiner
Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes.
July 2002, Organic letters,
E Hannig, and R Heyde, and H Matschiner
N4 -aryl substituted thiosemicarbazones derived from 1-indanones as potential anti-tumor agents for breast cancer treatment.
June 2018, Journal of cellular physiology,
E Hannig, and R Heyde, and H Matschiner
Fischer Carbene Pentannulation with Alkynes Having Adjacent Carbonate or Acyloxy Groups: Synthesis of 3-Substituted 1-Indanones.
May 2020, Organic letters,
E Hannig, and R Heyde, and H Matschiner
1-substituted 2-heteroadamantanes.
April 1969, Tetrahedron letters,
Copied contents to your clipboard!