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  2. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    Formyl functional group is shown in blue. Formylation refers to any chemical processes in which a compound is functionalized with a formyl group (-CH=O). In organic chemistry, the term is most commonly used with regards to aromatic compounds (for example the conversion of benzene to benzaldehyde in the Gattermann–Koch reaction).

  3. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.

  4. Ferrocenecarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/Ferrocenecarboxaldehyde

    Ferrocenecarboxaldehyde, owing to the versatility of the formyl group, is a precursor to many ferrocene-modified compounds. With a Wittig reagent, it converts to vinylferrocene and related derivatives. [5] With primary amines, ferrocenecarboxaldehyde condenses to give imines. The azomethine derivative undergoes 1,3-cycloaddition to C 60. [6]

  5. Formic acid - Wikipedia

    en.wikipedia.org/wiki/Formic_acid

    Formic acid is a source for a formyl group for example in the formylation of N-methylaniline to N-methylformanilide in toluene. [20] In synthetic organic chemistry, formic acid is often used as a source of hydride ion, as in the Eschweiler–Clarke reaction: The Eschweiler–Clark reaction

  6. N-Formylmethionine - Wikipedia

    en.wikipedia.org/wiki/N-Formylmethionine

    N-Formylmethionine (fMet, [2] HCO-Met, [3] For-Met [3]) is a derivative of the amino acid methionine in which a formyl group has been added to the amino group. It is specifically used for initiation of protein synthesis from bacterial and organellar genes, and may be removed post-translationally.

  7. Category:Formylation reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Formylation_reactions

    In chemistry a formylation reaction is a class of addition reaction, in which a formyl group is added to a substituent to give an aldehyde. Pages in category "Formylation reactions" The following 8 pages are in this category, out of 8 total.

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  9. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    If the carbon in the carbonyl group cannot be included in the attached chain (for instance in the case of cyclic aldehydes), the prefix "formyl-" or the suffix "-carbaldehyde" is used: C 6 H 11 CHO is cyclohexanecarbaldehyde. If an aldehyde is attached to a benzene and is the main functional group, the suffix becomes benzaldehyde.