1975
DOI: 10.1021/ja00855a053
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Polyamide supports for polypeptide synthesis

Abstract: The weak extinction coefficient (r ~100) observed for this band20•21 would indicate that the transition is probably dipole forbidden. ( 23) Queen Elizabeth II Fellow, 1973-1975

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Cited by 223 publications
(88 citation statements)
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“…Consequently a wide range of chemically different supports used in a range of different physical formats had to be developed to address specific performance needs. 33 and polyether crosslinked polyacylamides (PEGA) 34 exhibit excellent compatibility with hydrophilic solvents, responsible for their excellent performance in peptide synthesis. However these supports have only limited general applicability due to their lack of chemical stability (amide groups) under reaction conditions usually encountered in organic synthesis, which precludes their use in SPOS.…”
Section: Abstract: Novel Non-peg Derived Polyether Resins Coined Slumentioning
confidence: 99%
“…Consequently a wide range of chemically different supports used in a range of different physical formats had to be developed to address specific performance needs. 33 and polyether crosslinked polyacylamides (PEGA) 34 exhibit excellent compatibility with hydrophilic solvents, responsible for their excellent performance in peptide synthesis. However these supports have only limited general applicability due to their lack of chemical stability (amide groups) under reaction conditions usually encountered in organic synthesis, which precludes their use in SPOS.…”
Section: Abstract: Novel Non-peg Derived Polyether Resins Coined Slumentioning
confidence: 99%
“…The cross linked t-butoxycarbonyl(BOC)-&alanyl-hexamethylenediamine-polydimethylacrylamide resin was prepared essentially as described previously [6], but on a ten-fold scale. On this larger scale, the polymer was obtained in a largely amorphous rather than beaded form.…”
Section: Preparation Of Resinmentioning
confidence: 99%
“…The /3-alanine content was 0.24 mmol/g. The terminal BOC-group was removed by subjecting the resin to steps l-8 of the solid phase synthesis cycle [6] prior to activation of the resin. Dimethylacetamide was used in place of dimethylformamide [6].…”
Section: Preparation Of Resinmentioning
confidence: 99%
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“…[20][21][22][23] We will discuss the synthesis of the aminofunctional SLURPS first, followed by linker conjugation, as this has not been reported before, followed by our SPPS of Leu-enkephalin.…”
Section: Introductionmentioning
confidence: 99%