Amino Acids, Peptides and Proteins in Organic Chemistry 2010
DOI: 10.1002/9783527631803.ch6
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Solution‐Phase Peptide Synthesis

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Cited by 5 publications
(3 citation statements)
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“…In solution phase synthesis, two amino acids are coupled in solution, the first being protected at the carboxyl group and the second protected at the N-terminus group [36]. Before each addition of amino acids, the intermediate peptides are isolated, purified and characterized; the N-terminus protective group is removed to allow coupling with the next N-terminus protected amino acid.…”
Section: Synthetic and Recombinant Peptidesmentioning
confidence: 99%
“…In solution phase synthesis, two amino acids are coupled in solution, the first being protected at the carboxyl group and the second protected at the N-terminus group [36]. Before each addition of amino acids, the intermediate peptides are isolated, purified and characterized; the N-terminus protective group is removed to allow coupling with the next N-terminus protected amino acid.…”
Section: Synthetic and Recombinant Peptidesmentioning
confidence: 99%
“…It also suffers poor green credentials: protecting groups, atom inefficiency, high E-factor and low process mass intensity, Scheme 1b, Table 2. [12][13][14] Biosynthesis methods are leading the way in synthesis of longer peptides, for example in insulin manufacture, 15 but are unproductive for short peptides. For example proteases are used to couple protected amino acids, but rely on high enzyme loadings and displacing unfavourable equilibria with either excess reagents, solubility effects or organic solvents, Scheme 1c.…”
Section: Introductionmentioning
confidence: 99%
“…On the other hand, organic solution phase synthesis (SPS), which uses similar chemical methodology to SPPS, is the main method for small peptide manufacture. It also suffers poor green credentials: protecting groups, atom inefficiency, a high E-factor, and low process mass intensity, Scheme b, Table . Biosynthesis methods are leading the way in synthesis of longer peptides, for example in insulin manufacture, but are unproductive for short peptides. For example proteases are used to couple protected amino acids, but rely on high enzyme loadings and displacing unfavorable equilibria with either excess reagents, solubility effects, or organic solvents, Scheme c. , Surprisingly, the pioneering work done in the 1950–60s by Bartlett and Hirschmann describing the coupling of N -carboxyanhydride (NCA or Leuch’s anhydride) to amino acids has not been widely adopted, despite it being productive, cost-effective, and green, Scheme . …”
Section: Introductionmentioning
confidence: 99%