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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. The ring expansion occurs in the second step, with an electrocyclic reaction opening the cyclopropane ring to form the 7 ...

  3. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

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

    The Büchner ring expansion reactions utilizing diazoalkanes have proven to be synthetically useful as they can not only be used to form 5- and 6-membered rings, but also more unstable 7- and 8-membered rings. [27] The Büchner–Curtius–Schlotterbeck reaction used in one Carbon ring expansions

  4. Ring expansion and contraction - Wikipedia

    en.wikipedia.org/wiki/Ring_expansion_and_contraction

    The Buchner ring expansion is encouraged to open to the desired product by placing electron withdrawing groups on the carbon added. In order to perform the ring opening on saturated bicyclic molecules the cyclopropane must be introduced such that a neighboring group can facilitate the expansion or the ring must be opened by attackate the ...

  5. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    Case 3 & 4: the single atom is the sulfur in sulfur dioxide (SO 2), which joins the alkene chains to form a ring. In organic chemistry , cheletropic reactions , also known as chelotropic reactions , [ 2 ] are a type of pericyclic reaction (a chemical reaction that involves a transition state with a cyclic array of atoms and an associated cyclic ...

  6. Category:Ring expansion reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Ring_expansion...

    Pages in category "Ring expansion reactions" The following 6 pages are in this category, out of 6 total. ... Buchner ring expansion; D. Dowd–Beckwith ring-expansion ...

  7. Electrocyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Electrocyclic_reaction

    Reactions can be either ring-opening or ring-closing (electrocyclization). Depending on the type of reaction (photochemical or thermal) and the number of pi electrons, the reaction can happen through either a conrotatory or disrotatory mechanism. The type of rotation determines whether the cis or trans isomer of the product will be formed.

  8. Addition reaction - Wikipedia

    en.wikipedia.org/wiki/Addition_reaction

    In organic chemistry, an addition reaction is an organic reaction in which two or more molecules combine to form a larger molecule called the adduct. [1] [2]An addition reaction is limited to chemical compounds that have multiple bonds.

  9. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    Ring forming reaction: Identifiers RSC ontology ID The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [1] [2] ...