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Volumn 13, Issue 11, 2007, Pages 742-748

1,4-Diazepine-2,5-dione ring formation during solid phase synthesis of peptides containing aspartic acid β-benzyl ester

Author keywords

1,4 diazepine 2,5 dione peptides; Aspartimide; Fmoc technique; SPPS

Indexed keywords

1,4 DIAZEPINE 2,5 DIONE; 9 FLUORENYLMETHYL CHLOROFORMATE; AMINO ACID; ASPARTIC ACID; DIAZEPINE DERIVATIVE; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 36048936251     PISSN: 10752617     EISSN: 10991387     Source Type: Journal    
DOI: 10.1002/psc.885     Document Type: Article
Times cited : (11)

References (5)
  • 2
    • 0018623326 scopus 로고
    • Formation of aminosuccinyl peptides during acidolytic deprotection followed by their transformation to piperazine-2,5-dione derivatives in neutral media
    • Schon I, Kisfaludy L. Formation of aminosuccinyl peptides during acidolytic deprotection followed by their transformation to piperazine-2,5-dione derivatives in neutral media. Int. J. Pept. Protein Res. 1979; 14: 485-494.
    • (1979) Int. J. Pept. Protein Res , vol.14 , pp. 485-494
    • Schon, I.1    Kisfaludy, L.2
  • 5
    • 27144504450 scopus 로고    scopus 로고
    • The aspartimide problem in Fmoc-based SPPS. Part III
    • Mergler M, Dick F. The aspartimide problem in Fmoc-based SPPS. Part III. J. Pept. Sci. 2005; 11: 650-657.
    • (2005) J. Pept. Sci , vol.11 , pp. 650-657
    • Mergler, M.1    Dick, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.