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  2. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    Triethylamine is commonly used in the production of anionic Polyurethane dispersions (resins dispersed in water rather than solvents) as a neutralizing agent.. Triethylamine is used to give salts of various carboxylic acid-containing pesticides, e.g. Triclopyr and 2,4-dichlorophenoxyacetic acid.

  3. File:Organic Chemistry.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Organic_Chemistry.pdf

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  4. Enamine - Wikipedia

    en.wikipedia.org/wiki/Enamine

    Enamines chemistry has been implemented for the purposes of producing a one-pot enantioselective version of the Robinson annulation. The Robinson annulation, published by Robert Robinson in 1935, is a base-catalyzed reaction that combines a ketone and a methyl vinyl ketone (commonly abbreviated to MVK) to form a cyclohexenone fused ring system.

  5. Adenosine monophosphate - Wikipedia

    en.wikipedia.org/wiki/Adenosine_monophosphate

    Adenosine monophosphate (AMP), also known as 5'-adenylic acid, is a nucleotide.AMP consists of a phosphate group, the sugar ribose, and the nucleobase adenine.It is an ester of phosphoric acid and the nucleoside adenosine. [1]

  6. S-Adenosyl methionine - Wikipedia

    en.wikipedia.org/wiki/S-Adenosyl_methionine

    Depending on the enzyme, S-adenosyl methionine can be converted into one of three products: adenosyl radical, which converts to deoxyadenosine (AdO): classic rSAM reaction, also cogenerates methionine; S-adenosyl homocysteine, releasing methyl radical; methylthioadenosine (SMT), homoalanine radical

  7. Libration (molecule) - Wikipedia

    en.wikipedia.org/wiki/Libration_(molecule)

    In physics and chemistry, a molecule (or other group of atoms) can undergo libration if it is subject to external forces or constraints that restrict its orientation. For example, in liquid water, any given water molecule is attracted to neighboring molecules, so that it has a preferred orientation and cannot freely rotate. (Of course, over ...

  8. Enantioselective synthesis - Wikipedia

    en.wikipedia.org/wiki/Enantioselective_synthesis

    Enantioselective synthesis, also called asymmetric synthesis, [1] is a form of chemical synthesis.It is defined by IUPAC as "a chemical reaction (or reaction sequence) in which one or more new elements of chirality are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereomeric) products in unequal amounts."

  9. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    Free radicals derived from mercaptans, called thiyl radicals, are commonly invoked to explain reactions in organic chemistry and biochemistry. They have the formula RS • where R is an organic substituent such as alkyl or aryl. [6] They arise from or can be generated by a number of routes, but the principal method is H-atom abstraction from ...