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  2. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    The Buchner ring expansion is a two-step organic C-C bond forming reaction used to access 7-membered rings. The first step involves formation of a carbene from ethyl diazoacetate , which cyclopropanates an aromatic ring.

  3. Metal-catalyzed cyclopropanations - Wikipedia

    en.wikipedia.org/wiki/Metal-catalyzed_cyclopropa...

    Definitive mechanistic studies of rhodium-catalyzed cyclopropanation are lacking. However, the mechanism has been rationalized based on product distribution and stereoselectivity. [4] Attack of the diazo compound on the metal center generates a zwitterionic metal alkyl complex, which expels nitrogen gas to afford a metal carbene intermediate.

  4. Cyclopropanation - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanation

    Cyclopropanation is also stereospecific as the addition of carbene and carbenoids to alkenes is a form of a cheletropic reaction, with the addition taking place in a syn manner. For example, dibromocarbene and cis -2-butene yield cis -2,3-dimethyl-1,1-dibromocyclopropane, whereas the trans isomer exclusively yields the trans cyclopropane.

  5. Divinylcyclopropane-cycloheptadiene rearrangement - Wikipedia

    en.wikipedia.org/wiki/Divinylcyclopropane...

    Cyclopropanation with conjugated diazo compounds produces divinylcyclopropanes that then undergo rearrangement. When cyclic starting materials are used, bridged products result. [12] (8) Substrates containing three-membered heterocyclic rings can also undergo the reaction. cis-Divinylepoxides give oxepines at elevated temperatures (100 °C).

  6. Cyclopropanes - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanes

    A second major route to cyclopropanes entails addition of methylene (or its substituted derivatives) to an alkene, a process called cyclopropanation. [3] Substituted cyclopropanes undergo the reactions associated with the cyclopropyl ring or the substituents. Vinylcyclopropanes are a special case as they undergo vinylcyclopropane rearrangement.

  7. Intramolecular reactions of diazocarbonyl compounds - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_reactions...

    The reaction mechanism of decomposition of diazocarbonyl compounds with copper begins with the formation of a copper carbene complex. Evidence for the formation of copper carbenes is provided by comparison to the behavior of photolytically generated free carbenes [6] and the observation of appreciable enantioselectivity in cyclopropanations with chiral copper complexes. [7]

  8. Treatment Improvement Protocols - Wikipedia

    en.wikipedia.org/.../Treatment_Improvement_Protocols

    Treatment Improvement Protocols (TIPs) are a series of best-practice manuals for the treatment of substance use and other related disorders. The TIP series is published by the Substance Abuse and Mental Health Services Administration (SAMHSA), an operational division of the U.S. Department of Health and Human Services .

  9. Cyclopropane - Wikipedia

    en.wikipedia.org/wiki/Cyclopropane

    Cyclopropane is the cycloalkane with the molecular formula (CH 2) 3, consisting of three methylene groups (CH 2) linked to each other to form a triangular ring.The small size of the ring creates substantial ring strain in the structure.