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Volumn 74, Issue 3, 2009, Pages 1329-1332

An automatic solid-phase synthesis of peptaibols

Author keywords

[No Author keywords available]

Indexed keywords

ALAMETHICIN; AUTOMATED APPROACHES; AUTOMATED SYNTHESIS; MICROWAVE-ASSISTED; PEPTAIBOLS; SOLID-PHASE PEPTIDE SYNTHESIS; SOLID-PHASE SYNTHESIS; SYNTHESIS TIME;

EID: 64549121152     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802058x     Document Type: Article
Times cited : (50)

References (27)
  • 8
    • 34447536548 scopus 로고    scopus 로고
    • For special journal issues on peptaibols, see: Chem. Biodiversity 2007, 4, 1021-1412; J. Pept. Sci. 2003, 9, 659-837.
    • For special journal issues on peptaibols, see: Chem. Biodiversity 2007, 4, 1021-1412; J. Pept. Sci. 2003, 9, 659-837.
  • 9
    • 0345169940 scopus 로고    scopus 로고
    • A peptaibol database exists: Whitmore, L.; Chugh, J. K.; Snook, C. F.; Wallace, B. A. J. Pent. Sci. 2003, 9, 663-665. See also http://www.cryst.b-bk.ac.uk/peptaibol.
    • A peptaibol database exists: Whitmore, L.; Chugh, J. K.; Snook, C. F.; Wallace, B. A. J. Pent. Sci. 2003, 9, 663-665. See also http://www.cryst.b-bk.ac.uk/peptaibol.
  • 13
    • 0011621903 scopus 로고    scopus 로고
    • Selected examples: (a) Gisin, B. F.; Davis, D. G.; Borowska, Z. K.; Hall, J. E.; Kobayashi, S. J. Am. Chem. Soc. 1981, 103, 6373-6377.
    • Selected examples: (a) Gisin, B. F.; Davis, D. G.; Borowska, Z. K.; Hall, J. E.; Kobayashi, S. J. Am. Chem. Soc. 1981, 103, 6373-6377.
  • 22
    • 42149124280 scopus 로고    scopus 로고
    • Vosegaard, T.; Bertelsen, K.; Pedersen, J. M.; Th0gersen, L.; Schi0tt, B.; Tajkhorshid, E.; Skrydstrup, T.; Nielsen, N. C. J. Am. Chem. Soc. 2008, 130, 5028-5029.
    • (b) Vosegaard, T.; Bertelsen, K.; Pedersen, J. M.; Th0gersen, L.; Schi0tt, B.; Tajkhorshid, E.; Skrydstrup, T.; Nielsen, N. C. J. Am. Chem. Soc. 2008, 130, 5028-5029.
  • 26
    • 64549162361 scopus 로고    scopus 로고
    • The lower yield obtained in the synthesis of tylopeptin A is due to the fact that considerable amounts of the Iva deletion product were obtained. Two peaks were observed for the purified tylopeptin A due to the presence of two epimers of this peptide as racemic Iva was employed
    • The lower yield obtained in the synthesis of tylopeptin A is due to the fact that considerable amounts of the Iva deletion product were obtained. Two peaks were observed for the purified tylopeptin A due to the presence of two epimers of this peptide as racemic Iva was employed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.