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  2. Aziridine - Wikipedia

    en.wikipedia.org/wiki/Aziridine

    Aziridine is an organic compound consisting of the three-membered heterocycle C 2 H 5 N. [ 5 ] [ 6 ] It is a colorless, toxic, volatile liquid that is of significant practical interest. [ 7 ] Aziridine was discovered in 1888 by the chemist Siegmund Gabriel . [ 8 ]

  3. Aziridines - Wikipedia

    en.wikipedia.org/wiki/Aziridines

    Mitomycin C, an aziridine, is used as a chemotherapeutic agent by virtue of its antitumour activity. [1]In organic chemistry, aziridines are organic compounds containing the aziridine functional group (chemical structure (R−) 4 C 2 N−R), a three-membered heterocycle with one amine (>NR) and two methylene bridges (>CR 2).

  4. C2H5N - Wikipedia

    en.wikipedia.org/wiki/C2H5N

    Aziridine; Ethanimine or its tautomer, vinylamine; N-Methylmethanimine This page was last edited on 27 December 2022, at 20:58 (UTC). Text is available under ...

  5. Bucherer–Bergs reaction - Wikipedia

    en.wikipedia.org/wiki/Bucherer–Bergs_reaction

    This reaction has three points of chemical diversity as the structure of the aziridine starting compound, the organometallic reagent, and the electrophile can all be varied to synthesize a different hydantoin. [6]

  6. Azirine - Wikipedia

    en.wikipedia.org/wiki/Azirine

    Azirines are three-membered heterocyclic unsaturated (i.e. they contain a double bond) compounds containing a nitrogen atom and related to the saturated analogue aziridine. [1] They are highly reactive yet have been reported in a few natural products such as Dysidazirine.

  7. Aziridinium - Wikipedia

    en.wikipedia.org/wiki/Aziridinium

    Aziridiniums are the ionic form of the class of molecules known as aziridines. [1] Aziridines can be used to insert nitrogen atoms during synthesis, but without any substituents attached to the nitrogen in the ring, they are considered nonactivated and inert. [2] They can be rendered active by the preparation of aziridinium ions.

  8. Mitomycins - Wikipedia

    en.wikipedia.org/wiki/Mitomycins

    Chemical structure of mitomycin C. The mitomycins are a family of aziridine-containing natural products isolated from Streptomyces caespitosus or Streptomyces lavendulae. [1] [2] They include mitomycin A, mitomycin B, and mitomycin C. When the name mitomycin occurs alone, it usually refers to mitomycin C, its international nonproprietary name ...

  9. Blum–Ittah aziridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Blum–Ittah_aziridine...

    The Blum–Ittah aziridine synthesis, also known as the Blum–Ittah-Shahak aziridine synthesis [1] or simply the Blum aziridine synthesis is a name reaction of organic chemistry, for the generation of aziridines from oxiranes.