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  2. Organic Reactions - Wikipedia

    en.wikipedia.org/wiki/Org._React.

    Organic Reactions is a peer-reviewed book series that was established in 1942. It publishes detailed descriptions of useful organic reactions . Each article (called a chapter) is an invited review of the primary source material for the given reaction, and is written under tight editorial control, making it a secondary to tertiary‑level source.

  3. Jacobsen rearrangement - Wikipedia

    en.wikipedia.org/wiki/Jacobsen_rearrangement

    Organic Reactions I: The Jacobsen Reaction (Wiley, 1942) M B Smith, J March. March's Advanced Organic Chemistry (Wiley, 2001) (ISBN 0-471-58589-0) W Pötsch. Lexikon bedeutender Chemiker (VEB Bibliographisches Institut Leipzig, 1989) (ISBN 3817110553

  4. Reactions of organocopper reagents - Wikipedia

    en.wikipedia.org/wiki/Reactions_of_organocopper...

    Reactions of organocopper reagents involve species containing copper-carbon bonds acting as nucleophiles in the presence of organic electrophiles. Organocopper reagents are now commonly used in organic synthesis as mild, selective nucleophiles for substitution and conjugate addition reactions.

  5. Organic Syntheses - Wikipedia

    en.wikipedia.org/wiki/Organic_Syntheses

    Organic Syntheses is a peer-reviewed scientific journal that was established in 1921. It publishes detailed and checked procedures for the synthesis of organic compounds.A unique feature of the review process is that all of the data and experiments reported in an article must be successfully repeated in the laboratory of a member of the editorial board as a check for reproducibility prior to ...

  6. Chan–Lam coupling - Wikipedia

    en.wikipedia.org/wiki/Chan–Lam_coupling

    Reaction example of Chan–Lam coupling. Compound 1, a pyrrole, is coupled with aryl boronic acid, 2, to afford product 3, which is then carried forward to the target 4. The nitrile group of 2 does not poison the catalyst. Pyridine is the ligand used for the reaction. Although the reaction requires three days, it was carried out at room ...

  7. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

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

    The reaction has since been modified to proceed in the presence of Lewis acids and common organic solvents such as THF and dichloromethane. Reactions generally run at room temperature for about an hour, and the yield ranges from 70%-80% based on the choice of Lewis acid and solvent. [10]

  8. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    The cheletropic reactions of 1,3-dienes with sulfur dioxide have been extensively investigated in terms of kinetics (see above for general reaction). In the first quantitative measurement of kinetic parameters for this reaction, a 1976 study by Isaacs and Laila measured the rates of addition of sulfur dioxide to butadiene derivatives.

  9. Name reaction - Wikipedia

    en.wikipedia.org/wiki/Name_reaction

    A name reaction (or named reaction) is a chemical reaction named after its discoverer(s) or developer(s). Among the tens of thousands of organic reactions that are known, hundreds of such reactions are typically identified by the eponym . [ 1 ]