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Peptide synthesis using o-nitrophenylsulfenyl N-carboxy .alpha.-amino acid anhydrides

✍ Scribed by Katakai, Ryoichi

Book ID
126438992
Publisher
American Chemical Society
Year
1975
Tongue
English
Weight
791 KB
Volume
40
Category
Article
ISSN
0022-3263

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📜 SIMILAR VOLUMES

Synthesis of N-protected peptides by the
Synthesis of N-protected peptides by the o-nitrophenylsulfenyl group using o-nitrophenylsulfenyl N-carboxy α-amino acid anhydrides
✍ Ryoichi Katakai; Masanao Oya 📂 Article 📅 1975 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 482 KB 👁 1 views

## Abstract __N__‐protected peptides, which are important intermediates as a carboxyl component in the fragment condensation method, have been prepared in high yields by the reaction of __o__‐nitrophenylsulfenyl (Nps) __N__‐carboxy α‐amino acid anhydrides with unprotected peptides and amino acids i

Peptide synthesis using o-nitrophenylsul
Peptide synthesis using o-nitrophenylsulfenyl N-carboxy α-amino acid anhydrides. Sequential oligopeptides having alternate γ-methyl L-glutamyl and L-phenylalanyl residues
✍ Ryoichi Katakai; Yohko Nakayama 📂 Article 📅 1976 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 494 KB 👁 1 views

## Abstract A series of sequential oligopeptides having the sequence alternating γ‐methyl L‐glutamyl and L‐phenylalanyl residues have been successfully prepared by a rapid method involving the reaction of __o__‐nitrophenylsulfenyl __N__‐carboxy α‐amino acid anhydrides with amino acid and peptide es