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  2. Isocyanide - Wikipedia

    en.wikipedia.org/wiki/Isocyanide

    An isocyanide (also called isonitrile or carbylamine) is an organic compound with the functional group – N + ≡C −. It is the isomer of the related nitrile (–C≡N), hence the prefix is isocyano. [1] The organic fragment is connected to the isocyanide group through the nitrogen atom, not via the carbon. They are used as building blocks ...

  3. Isocyanate - Wikipedia

    en.wikipedia.org/wiki/Isocyanate

    Curtius rearrangement degradation of an acyl azide to an isocyanate and nitrogen gas. Lossen rearrangement, the conversion of a hydroxamic acid to an isocyanate via the formation of an O-acyl, sulfonyl, or phosphoryl intermediate. An isocyanate is also the immediate product of the Hofmann rearrangement, but typically hydrolyzes under reaction ...

  4. Bioorthogonal chemistry - Wikipedia

    en.wikipedia.org/wiki/Bioorthogonal_chemistry

    This isocyanide click reaction is a [4+1] cycloaddition followed by a retro-Diels Alder elimination of N 2. [12] The reaction proceeds with an initial [4+1] cycloaddition followed by a reversion to eliminate a thermodynamic sink and prevent reversibility. This product is stable if a tertiary amine or isocyanopropanoate is used.

  5. Carbylamine reaction - Wikipedia

    en.wikipedia.org/wiki/Carbylamine_reaction

    In this context, the reaction is also known as Saytzeff's isocyanide test. [2] In this reaction, the analyte is heated with alcoholic potassium hydroxide and chloroform. If a primary amine is present, the isocyanide (carbylamine) is formed, as indicated by a foul odour. The carbylamine test does not give a positive reaction with secondary and ...

  6. Curtius rearrangement - Wikipedia

    en.wikipedia.org/wiki/Curtius_rearrangement

    Following hydrolysis of the ester in the intermediate (1), a Curtius rearrangement was effected to convert the carboxylic acid groups in (2) to the methyl carbamate groups (3) with 84% yield. Further steps then gave triquinacene (4). [27] The Curtius reaction in Woodward's total synthesis of triquinacene

  7. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    In a similar fashion, the intermediate isocyanate can be trapped by tert-butyl alcohol, yielding the tert-butoxycarbonyl (Boc)-protected amine. The Hofmann Rearrangement also can be used to yield carbamates from α,β - unsaturated or α- hydroxy amides [ 2 ] [ 8 ] or nitriles from α,β- acetylenic amides [ 2 ] [ 9 ] in good yields (≈70%).

  8. Prediabetes for Men: Everything You Need to Know, From ...

    www.aol.com/prediabetes-men-everything-know...

    Glucose Tolerance and Random Plasma Glucose Test. An oral glucose tolerance test checks how your body responds to glucose. Your blood glucose levels are measured before you consume 75 grams of ...

  9. Nef reaction - Wikipedia

    en.wikipedia.org/wiki/Nef_reaction

    In organic chemistry, the Nef reaction is an organic reaction describing the acid hydrolysis of a salt of a primary or secondary nitroalkane (R−NO 2) to an aldehyde (R−CH=O) or a ketone (R 2 C=O) and nitrous oxide (N 2 O). The reaction has been the subject of several literature reviews. [1] [2] [3] The Nef reaction: 1. Salt of a nitroalkane ...