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Volumn , Issue 4, 2008, Pages 513-516

Chemoenzymatic and chemical routes to the nonproteinaceous amino acid albizziine and its amide derivative

Author keywords

Amidation; D amino acid oxidase; Hoffmann rearrangement; Urea formation

Indexed keywords

ALBIZZIIN; AMIDE; AMINO ACID DERIVATIVE; ASPARAGINE DERIVATIVE; NATURAL PRODUCT; UNCLASSIFIED DRUG; ZWITTERMICIN A;

EID: 40949121537     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1042756     Document Type: Article
Times cited : (9)

References (40)
  • 24
    • 0029147529 scopus 로고    scopus 로고
    • The enantiomeric excess was determined through precolumn derivatisation with o-phthalaldehyde (OPA) and N- isobutyryl-L-cysteine (IBC) and analysis on a conventional 5μ C-18 reverse-phase HPLC column, see: Brückner, H.; Westhauser, T.; Godel, H. J. Chromatogr., A 1995, 711, 201.
    • The enantiomeric excess was determined through precolumn derivatisation with o-phthalaldehyde (OPA) and N- isobutyryl-L-cysteine (IBC) and analysis on a conventional 5μ C-18 reverse-phase HPLC column, see: Brückner, H.; Westhauser, T.; Godel, H. J. Chromatogr., A 1995, 711, 201.
  • 39
    • 40949123528 scopus 로고    scopus 로고
    • 2, or HCl-dioxane, was found to be unsuccessful in this instance.
    • 2, or HCl-dioxane, was found to be unsuccessful in this instance.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.