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  2. 2,4-Dimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2,4-Dimethoxybenzaldehyde

    2,4-Dimethoxybenzaldehyde (DMBA) is a reagent used to specifically quantify phlorotannins. This product reacts specifically with 1,3-and 1,3,5-substituted phenols (e.g., phlorotannins) to form a colored product. [1]

  3. Mitsunobu reaction - Wikipedia

    en.wikipedia.org/wiki/Mitsunobu_reaction

    The reaction mechanism of the Mitsunobu reaction is fairly complex. The identity of intermediates and the roles they play has been the subject of debate. Initially, the triphenyl phosphine (2) makes a nucleophilic attack upon diethyl azodicarboxylate (1) producing a betaine intermediate 3, which deprotonates the carboxylic acid (4) to form the ion pair 5.

  4. Henry reaction - Wikipedia

    en.wikipedia.org/wiki/Henry_reaction

    It is nearly analogous to the aldol reaction that had been discovered 23 years prior that couples two carbonyl compounds to form β-hydroxy carbonyl compounds known as "aldols" (aldehyde and alcohol). [2] [4] The Henry reaction is a useful technique in the area of organic chemistry due to the synthetic utility of its corresponding products, as ...

  5. 3,4,5-Trimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3,4,5-Trimethoxybenzaldehyde

    3,4,5-Trimethoxybenzaldehyde can be used as an intermediate in the synthesis of some pharmaceutical drugs including trimethoprim, [1] [2] cintriamide, roletamide, trimethoquinol (aka tretoquinol), and trimazosin as well as some psychedelic phenethylamines. [3] [4] [5]

  6. Diphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Diphenylmethanol

    Diphenylmethanol may be prepared by a Grignard reaction between phenylmagnesium bromide and benzaldehyde [citation needed]. An alternative method involves reducing benzophenone with sodium borohydride or with zinc dust or with sodium amalgam and water.

  7. Lignin peroxidase - Wikipedia

    en.wikipedia.org/wiki/Lignin_peroxidase

    The systematic name of this enzyme class is 1,2-bis(3,4-dimethoxyphenyl)propane-1,3-diol:hydrogen-peroxide oxidoreductase. Other names in common use include diarylpropane oxygenase , ligninase I , diarylpropane peroxidase , LiP , diarylpropane:oxygen,hydrogen-peroxide oxidoreductase (C-C-bond-cleaving) .

  8. Baylis–Hillman reaction - Wikipedia

    en.wikipedia.org/wiki/Baylis–Hillman_reaction

    [1] [2] Baylis-Hillman reaction. The reaction is named for Anthony B. Baylis and Melville E. D. Hillman, two of the chemists who developed the reaction at Celanese; and K. Morita, who published earlier work [3] on the same. The MBH reaction offers several advantages in organic synthesis: It combines easily prepared starting materials with high ...

  9. Dimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Dimethoxybenzaldehyde

    Dimethoxybenzaldehyde may refer to: 2,4-Dimethoxybenzaldehyde (DMBA) 2,5-Dimethoxybenzaldehyde; Veratraldehyde (3,4-dimethoxybenzaldehyde) This page was last edited ...