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Volumn 38, Issue 2, 1997, Pages 299-302

Simple methods for the preparation of protected derivatives of D-allo- and L-allo-threonine

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE;

EID: 0031012284     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(96)02297-6     Document Type: Article
Times cited : (3)

References (22)
  • 2
  • 14
    • 0015522445 scopus 로고
    • Abbreviations for amino acids used in this paper are those recommended by the IUPAC-IUPAB Commission of Biochemical Nomenclature, and published in J. Biol. Chem., 1972, 247, 977-983. Additional abbreviations used are: Ac, acetyl; Boc, tert-butoxycarbonyl; Bzl, benzyl; HPLC, high performance liquid chromatography; SPPS, solid-phase peptide synthesis; TFA, trifluoroacetic acid.
    • (1972) J. Biol. Chem. , vol.247 , pp. 977-983
  • 15
    • 0342866771 scopus 로고    scopus 로고
    • All new compounds gave satisfactory elemental analyses and physical data
    • All new compounds gave satisfactory elemental analyses and physical data.
  • 19
    • 0342866770 scopus 로고    scopus 로고
    • note
    • 22 This latter allowed all four diastereomers of Thr to be cleanly separated. Synthetic allo-threonines were judged to contain less than 0.5 % of their corresponding enantiomers.
  • 20
    • 0343301852 scopus 로고    scopus 로고
    • Hydrolysis of 277 mg of a mixture of 8 and 12, required 103 mg of enzyme in total, and was complete in 3 days
    • Hydrolysis of 277 mg of a mixture of 8 and 12, required 103 mg of enzyme in total, and was complete in 3 days.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.