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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. 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.

  4. Late onset congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Late_onset_congenital...

    Late onset congenital adrenal hyperplasia (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of congenital adrenal hyperplasia (CAH), [1] a group of autosomal recessive disorders characterized by impaired cortisol synthesis that leads to variable degrees of postnatal androgen excess.

  5. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

    en.wikipedia.org/wiki/Diffuse_idiopathic...

    The pathological definition published by the World Health Organization is “a generalized proliferation of scattered single cells, small nodules (neuroendocrine bodies), or linear proliferations of pulmonary neuroendocrine (PNE) cells that may be confined to the bronchial and bronchiolar epithelium.” [1] The true prevalence of this disease ...

  6. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    The Buchner–Curtius–Schlotterbeck reaction is the reaction of aldehydes or ketones with aliphatic diazoalkanes to form homologated ketones. [1] It was first described by Eduard Buchner and Theodor Curtius in 1885 [ 2 ] and later by Fritz Schlotterbeck in 1907. [ 3 ]

  7. 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.

  8. 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.

  9. Activation of cyclopropanes by transition metals - Wikipedia

    en.wikipedia.org/wiki/Activation_of_cyclopro...

    Structure of the platinacyclobutane PtC 3 H 6 (bipy) derived from activation of cyclopropane.. In organometallic chemistry, the activation of cyclopropanes by transition metals is a research theme with implications for organic synthesis and homogeneous catalysis. [1]