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  2. Claisen condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen_condensation

    The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base. The reaction produces a β-keto ester or a β-diketone. [1] It is named after Rainer Ludwig Claisen, who first published his work on the reaction in 1887.

  3. Fatty acid synthase - Wikipedia

    en.wikipedia.org/wiki/Fatty_acid_synthase

    n/a n/a Ensembl n/a n/a UniProt n a n/a RefSeq (mRNA) n/a n/a RefSeq (protein) n/a n/a Location (UCSC) n/a n/a PubMed search n/a n/a Wikidata View/Edit Human Fatty acid synthase (FAS) is an enzyme that in humans is encoded by the FASN gene. Fatty acid synthase is a multi-enzyme protein that catalyzes fatty acid synthesis. It is not a single enzyme but a whole enzymatic system composed of two ...

  4. Claisen–Schmidt condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen–Schmidt_condensation

    It can be considered as a specific variation of the aldol condensation. This reaction is named after two of its pioneering investigators Rainer Ludwig Claisen and J. Gustav Schmidt, who independently published on this topic in 1880 and 1881. [1] [2] [3] An example is the synthesis of dibenzylideneacetone ((1E, 4E)-1,5-diphenylpenta-1,4-dien-3 ...

  5. Rainer Ludwig Claisen - Wikipedia

    en.wikipedia.org/wiki/Rainer_Ludwig_Claisen

    The reaction is known as the Claisen reaction and was described by Claisen for the first time in 1890. Discovered the thermally induced rearrangement of allyl phenyl ether in 1912. He details its reaction mechanism in his last scientific publication (1925). In his honor, the reaction has been named the Claisen rearrangement.

  6. Claisen rearrangement - Wikipedia

    en.wikipedia.org/wiki/Claisen_rearrangement

    The Claisen rearrangement is a powerful carbon–carbon bond-forming chemical reaction discovered by Rainer Ludwig Claisen. [1] The heating of an allyl vinyl ether will initiate a [3,3]-sigmatropic rearrangement to give a γ,δ-unsaturated carbonyl, driven by exergonically favored carbonyl CO bond formation Δ(Δ f H) = −327 kcal/mol (−1,370 kJ/mol).

  7. Claisen ester condensations - Wikipedia

    en.wikipedia.org/?title=Claisen_ester...

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Claisen_ester_condensations&oldid=370027671"https://en.wikipedia.org/w/index.php?title=Claisen_ester

  8. NYT ‘Connections’ Hints and Answers Today, Wednesday, December 11

    www.aol.com/nyt-connections-hints-answers-today...

    1. An idyllic or picturesque place. 2. To function properly, these items require a vigorous, up-and-down motion before use. 3. A blending of names/terms to create something new. 4. The words in ...

  9. Claisen - Wikipedia

    en.wikipedia.org/wiki/Claisen

    Claisen may refer to: Rainer Ludwig Claisen, a German chemist Claisen rearrangement, a reaction of a allyl vinyl ether to a γ,δ-unsaturated carbonyl; Claisen condensation, a reaction between esters and carbonyl compounds in the presence of a strong base; Ireland–Claisen rearrangement, a chemical reaction of an allylic ester with strong base