On the use of PyAOP, a phosphonium salt derived from HOAt, in solid-phase peptide synthesis
β Scribed by Fernando Albericio; Marta Cases; Jordi Alsina; Salvatore A. Triolo; Louis A. Carpino; Steven A. Kates
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 293 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Phosphonium derivatives of HOAt such as PyAOP are useful for the solid-phase preparation of a range of peptides that include those incorporating hindered amino acids, difficult short sequences, and cyclic peptides. An advantage relative to uronium salts is that excess PyAOP does not undergo the detrimental side-reaction at the amino terminus which blocks further chain assembly.
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The 15-turn forming glycopeptide 6 from the homophilic recognition domain of mouse op, thelial cadherin 1 carrying a T~-antigen side chain was synthesised on solid phase using an allylic anchor and the new coupling reagent N.N-N;N'-bis(tetramethylene)-O-pentafluorophenyluronium hexafluorophosphate 3
## Abstract Sulfurization of protected [__i.e.__, 2βcyanoethyl, methyl and 2β(4βnitrophenyl)ethyl] internucleosidic phosphite triesters can be conveniently executed with the easily accessible reagent, phenylacetyl disulfide (1). Highβquality oligodeoxynucleotides containing predetermined combinatio