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  2. Ugi reaction - Wikipedia

    en.wikipedia.org/wiki/Ugi_reaction

    The Ugi reaction has been applied in combination with an intramolecular Diels-Alder reaction [16] in an extended multistep reaction. A reaction in its own right is the Ugi–Smiles reaction with the carboxylic acid component replaced by a phenol. In this reaction the Mumm rearrangement in the final step is replaced by the Smiles rearrangement. [17]

  3. Chemical synthesis - Wikipedia

    en.wikipedia.org/wiki/Chemical_synthesis

    These strategies can be grouped into approaches for managing reaction sequences. Reaction Sequences: Multistep synthesis involves sequential chemical reactions, each requiring its own work-up to isolate intermediates before proceeding to the next stage. [4] For example, the synthesis of paracetamol typically requires three separate reactions.

  4. Combinatorial chemistry - Wikipedia

    en.wikipedia.org/wiki/Combinatorial_chemistry

    Using the twenty natural amino acids, for example, in a tripeptide creates 8,000 (20 3) possibilities. Solid-phase methods for small molecules were later introduced and Furka devised a "split and mix" approach [2] [4] In its modern form, combinatorial chemistry has probably had its biggest impact in the pharmaceutical industry. [5]

  5. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined. Cross-couplings are a subset of the more general coupling reactions. Often cross-coupling reactions require metal catalysts. One important reaction type is this:

  6. Category:Chemical reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Chemical_reactions

    Salt metathesis reaction; Salt-free reduction; Scavenger resin; Screaming jelly babies; SEA Native Peptide Ligation; Self-assembling peptide; Semiclassical transition state theory; Shiina esterification; Side reaction; Single displacement reaction; Small molecule sensors; Solid-state reaction route; Spin-forbidden reactions; Stripping reaction ...

  7. Barton reaction - Wikipedia

    en.wikipedia.org/wiki/Barton_reaction

    The Barton reaction involves a homolytic RO–NO cleavage, followed by δ-hydrogen abstraction, free radical recombination, and tautomerization to form an oxime. [3] Selectivity for the δ-hydrogen is a result of the conformation of the 6-membered radical intermediate. Often, the site of hydrogen atom abstraction can be easily predicted.

  8. Multi-component reaction - Wikipedia

    en.wikipedia.org/wiki/Multi-component_reaction

    A multi-component reaction (or MCR), sometimes referred to as a "Multi-component Assembly Process" (or MCAP), is a chemical reaction where three or more compounds react to form a single product. [1] By definition, multicomponent reactions are those reactions whereby more than two reactants combine in a sequential manner to give highly selective ...

  9. Nef reaction - Wikipedia

    en.wikipedia.org/wiki/Nef_reaction

    Nef reaction in combination with Michael addition. In carbohydrate chemistry, they are a chain-extension method for aldoses, as in the isotope labeling of C 14-D‑mannose and C 14-D‑glucose from D‑arabinose and C 14 ‑nitromethane (the first step here is a Henry reaction): The Nef reaction: chain extension. The opposite reaction is the ...