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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. DMTMM - Wikipedia

    en.wikipedia.org/wiki/DMTMM

    Amide coupling is one of the most common reactions in organic chemistry and DMTMM is one reagent used for that reaction. The mechanism of DMTMM coupling is similar to other common amide coupling reactions involving activated carboxylic acids. [1] Its precursor, 2-chloro-4,6,-dimethoxy-1,3,5-triazine (CDMT), has also been used for amide coupling.

  4. Dimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Dimethoxybenzaldehyde

    2,5-Dimethoxybenzaldehyde; Veratraldehyde (3,4-dimethoxybenzaldehyde) This page was last edited on 17 March 2022, at 21:10 (UTC). Text is available under the ...

  5. Methylbenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Methylbenzaldehyde

    2-Methylbenzaldehyde (2-tolualdehyde) 3-Methylbenzaldehyde [Wikidata] (3-tolualdehyde) 4-Methylbenzaldehyde (4-tolualdehyde) This page was last edited on 14 May 2022 ...

  6. McMurry reaction - Wikipedia

    en.wikipedia.org/wiki/McMurry_reaction

    The reaction is named after its co-discoverer, John E. McMurry. The McMurry reaction originally involved the use of a mixture TiCl 3 and LiAlH 4, which produces the active reagents. Related species have been developed involving the combination of TiCl 3 or TiCl 4 with various other reducing agents, including potassium, zinc, and magnesium.

  7. Dimethoxymethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxymethane

    It can be manufactured by oxidation of methanol or by the reaction of formaldehyde with methanol. In aqueous acid, it is hydrolyzed back to formaldehyde and methanol.. Due to the anomeric effect, dimethoxymethane has a preference toward the gauche conformation with respect to each of the C–O bonds, instead of the anti conformation.

  8. Debus–Radziszewski imidazole synthesis - Wikipedia

    en.wikipedia.org/wiki/Debus–Radziszewski...

    The Debus–Radziszewski imidazole synthesis is a multi-component reaction used for the synthesis of imidazoles from a 1,2-dicarbonyl, an aldehyde, and ammonia or a primary amine. The method is used commercially to produce several imidazoles. [1] The process is an example of a multicomponent reaction. The reaction can be viewed as occurring in ...

  9. Dowd–Beckwith ring-expansion reaction - Wikipedia

    en.wikipedia.org/wiki/Dowd–Beckwith_ring...

    The Dowd–Beckwith ring-expansion reaction is an organic reaction in which a cyclic carbonyl (typically a β-keto ester) is expanded by up to 4 carbons in a free radical ring expansion reaction through an α-alkylhalo substituent. The radical initiator system is based on azobisisobutyronitrile and tributyltin hydride. [1]