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Volumn 120, Issue 14, 1998, Pages 3345-3356

One-electron photooxidation of N-methionyl peptides. Mechanism of sulfoxide and azasulfonium diastereomer formation through reaction of sulfide radical cation complexes with oxygen or superoxide

Author keywords

[No Author keywords available]

Indexed keywords

BENZOPHENONE DERIVATIVE; CATION; HYDROXYL RADICAL; METHIONINE; OXYGEN; PEPTIDE; RADICAL; SULFIDE; SULFONIUM DERIVATIVE; SULFOXIDE; SUPEROXIDE; SUPEROXIDE DISMUTASE;

EID: 0032522103     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja973084t     Document Type: Article
Times cited : (72)

References (62)
  • 23
    • 2642659859 scopus 로고    scopus 로고
    • note
    • Samples were acidified with DCl. At pD 2.2, azasulfonium derivatives undergo hydrolysis to the respective sulfoxides. However, NMR spectra of the AS derivatives can be recorded within 5 min after acidification to pD 2.2.
  • 28
    • 2642632205 scopus 로고    scopus 로고
    • note
    • 17


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.