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  2. Dimethylformamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylformamide

    Dimethylformamide, DMF is an organic compound with the chemical formula H C O N(CH 3) 2.Its structure is HC(=O)−N(−CH 3) 2.Commonly abbreviated as DMF (although this initialism is sometimes used for dimethylfuran, or dimethyl fumarate), this colourless liquid is miscible with water and the majority of organic liquids.

  3. Tris(pentafluorophenyl)borane - Wikipedia

    en.wikipedia.org/wiki/Tris(pentafluorophenyl)borane

    Tris(pentafluorophenyl)borane is a key reagent leading to the concept of frustrated Lewis pairs. The combination of BCF and bulky basic phosphines, such as tricyclohexylphosphine (PCy 3) cleaves H 2: [11] (C 6 F 5) 3 B + PCy 3 + H 2 → (C 6 F 5) 3 BH − + HPCy 3 + Many related phosphines, boranes, and substrates participate in related reactions.

  4. Bouveault aldehyde synthesis - Wikipedia

    en.wikipedia.org/wiki/Bouveault_aldehyde_synthesis

    The first step of the Bouveault aldehyde synthesis is the formation of the Grignard reagent. Upon addition of a N , N -disubstituted formamide (such as dimethylformamide ) a hemiaminal is formed, which can easily be hydrolyzed into the desired aldehyde.

  5. Dihydrolevoglucosenone - Wikipedia

    en.wikipedia.org/wiki/Dihydrolevoglucosenone

    Dihydrolevoglucosenone is considered a "green" replacement for DMF. [5] Several standard reactions of organic chemistry, e.g. Menshutkin reaction, [5] Sonogashira coupling, [18] Suzuki-Miyaura coupling [19] and the production of ureas [20] have been carried out in dihydrolevoglucosenone. Formation of ureas using dihydrolevoglucosenone as a solvent

  6. Borane dimethylsulfide - Wikipedia

    en.wikipedia.org/wiki/Borane_dimethylsulfide

    The advantages of BMS over other borane reagents, such as borane-tetrahydrofuran, are its increased stability and higher solubility. [1] BMS is commercially available at much higher concentrations than its tetrahydrofuran counterpart (10 M ) and does not require sodium borohydride as a stabilizer , which could result in undesired side reactions ...

  7. Propanephosphonic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Propanephosphonic_acid...

    The chemical is a useful reagent for peptide synthesis reactions, where it activates the carboxylic acid partner for subsequent reaction with amines. It is commercially available as 50 % solution in DMF or ethyl acetate as a slightly yellow mixture.

  8. HATU - Wikipedia

    en.wikipedia.org/wiki/HATU

    HATU (Hexafluorophosphate Azabenzotriazole Tetramethyl Uronium) is a reagent used in peptide coupling chemistry to generate an active ester from a carboxylic acid. HATU is used along with Hünig's base (N,N-diisopropylethylamine), or triethylamine to form amide bonds. Typically DMF is used as solvent, although other polar aprotic solvents can ...

  9. N-Methylformamide - Wikipedia

    en.wikipedia.org/wiki/N-Methylformamide

    N-Methylformamide (NMF) is a colorless, nearly odorless, organic compound and secondary amide with molecular formula CH 3 NHCHO, which is a liquid at room temperature. NMF is mainly used as a reagent in various organic syntheses with limited applications as a highly polar solvent.