메뉴 건너뛰기




Volumn 137, Issue 22, 2015, Pages 7197-7209

Chemical Protein Synthesis Using a Second-Generation N-Acylurea Linker for the Preparation of Peptide-Thioester Precursors

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CYCLIZATION; MICROWAVE HEATING; PEPTIDES; POLYPEPTIDES; PROTEINS; SURGICAL EQUIPMENT;

EID: 84935911053     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b03504     Document Type: Article
Times cited : (175)

References (94)
  • 22
  • 69
    • 84935873830 scopus 로고    scopus 로고
    • note
    • 2O in the solvents and under some conditions, i.e., 1 M DBU in DMF can lead to complete hydrolysis of the peptide.
  • 77
    • 84935881983 scopus 로고    scopus 로고
    • note
    • Interestingly, hydrolysis was only 15%, likely due to the rapid thiolysis of the anhydride intermediate.
  • 92
    • 84935914937 scopus 로고    scopus 로고
    • note
    • However, alkyl- and arylthioesters are more stable than N- acylureas which slowly hydrolyze even at acidic pH ∼ 2. Despite this lower stability, its purification, isolation, and handling are perfectly possible.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.