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  2. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    In organic chemistry, peptide synthesis is the production of peptides, compounds where multiple amino acids are linked via amide bonds, also known as peptide bonds. Peptides are chemically synthesized by the condensation reaction of the carboxyl group of one amino acid to the amino group of another.

  3. Solid-phase synthesis - Wikipedia

    en.wikipedia.org/wiki/Solid-phase_synthesis

    Solid-phase synthesis is a common technique for peptide synthesis.Usually, peptides are synthesised from the carbonyl group side (C-terminus) to amino group side (N-terminus) of the amino acid chain in the SPPS method, although peptides are biologically synthesised in the opposite direction in cells.

  4. Split and pool synthesis - Wikipedia

    en.wikipedia.org/wiki/Split_and_pool_synthesis

    The split and pool synthesis (S&P synthesis) differs from traditional synthetic methods. The important novelty is the use of compound mixtures in the process. This is the reason of its unprecedentedly high productivity. Using the method one single chemist can make more compounds in a week than all chemists produced in the whole history of ...

  5. Native chemical ligation - Wikipedia

    en.wikipedia.org/wiki/Native_chemical_ligation

    The key feature of native chemical ligation of unprotected peptides is the reversibility of the first step, the thiol(ate)–thioester exchange reaction. Native chemical ligation is exquisitely regioselective because that thiol(ate)–thioester exchange step is freely reversible in the presence of an added arylthiol catalyst.

  6. Combinatorial chemistry - Wikipedia

    en.wikipedia.org/wiki/Combinatorial_chemistry

    A "parallel synthesis" method was developed by Mario Geysen and his colleagues for preparation of peptide arrays. [19] They synthesized 96 peptides on plastic rods (pins) coated at their ends with the solid support. The pins were immersed into the solution of reagents placed in the wells of a microtiter plate. The method is widely applied ...

  7. Bailey peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Bailey_peptide_synthesis

    The Bailey peptide synthesis is a name reaction in organic chemistry developed 1949 by J. L. Bailey. [1] [2] It is a method for the synthesis of a peptide from α-amino acid-N-carboxylic acid anhydrides (NCAs) and amino acids or peptide esters. [2] [3] The reaction is characterized by short reaction times and a high yield of the target peptide. [2]

  8. Step-growth polymerization - Wikipedia

    en.wikipedia.org/wiki/Step-growth_polymerization

    The synthesis of first truly synthetic polymeric material, bakelite, was announced by Leo Baekeland in 1907, through a typical step-growth polymerization fashion of phenol and formaldehyde. The pioneer of synthetic polymer science, Wallace Carothers , developed a new means of making polyesters through step-growth polymerization in 1930s as a ...

  9. Bergmann azlactone peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Bergmann_azlactone_peptide...

    The Bergmann azlactone peptide synthesis is a classic organic synthesis process for the preparation of dipeptides. In the presence of a base, peptides are formed by aminolysis of N-carboxyanhydrides of amino acids with amino acid esters ( 1 ).