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Volumn 32, Issue 1, 1996, Pages 15-19

Stereoselective synthesis of L-[1-13C], L-[2-13C] and L-[15N] amino acids

Author keywords

Amino acids; Biochemistry; Carbon 13; Nitrogen 15; Nutrition; Stable isotopes; Stereochemistry; Synthesis

Indexed keywords

DRYOBALANOPS;

EID: 0001860058     PISSN: 10256016     EISSN: None     Source Type: Journal    
DOI: 10.1080/10256019608036289     Document Type: Article
Times cited : (7)

References (10)
  • 1
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    • (1983) Annu. Rev. Nutr. , vol.3 , pp. 309-339
    • Matthews, D.E.1    Bier, D.M.2
  • 2
    • 0024445477 scopus 로고
    • Asymmetric alkylations of a sultam-derived glycinate equivalent. Practical preparation of enantiomerically pure α-amino acids
    • and references herein
    • W. Oppolzer, R. Moretti, S. Thomi. Asymmetric alkylations of a sultam-derived glycinate equivalent. Practical preparation of enantiomerically pure α-amino acids. Tetrahedron Lett. 30 (1989) 6009-6010 and references herein
    • (1989) Tetrahedron Lett. , vol.30 , pp. 6009-6010
    • Oppolzer, W.1    Moretti, R.2    Thomi, S.3
  • 3
    • 0025936906 scopus 로고
    • Asymmetric synthesis of L-diphenylalanine and L-9-fluorenylglycine via room temperature alkylations of a sultam-derived glycine imine
    • H. Josien, A. Martin, G. Chassaing. Asymmetric synthesis of L-diphenylalanine and L-9-fluorenylglycine via room temperature alkylations of a sultam-derived glycine imine. Tetrahedron Lett. 32 (1991) 6547-6550
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6547-6550
    • Josien, H.1    Martin, A.2    Chassaing, G.3
  • 5
    • 0025191224 scopus 로고
    • Asymmetric synthesis of α-amino acids and α-N-hydroxyamino acids via electrophilic amination of bornane sultam-derived enolates with 1-chloro-1-nitrosocyclo hexane
    • W. Oppolzer, O. Tamura, Asymmetric synthesis of α-amino acids and α-N-hydroxyamino acids via electrophilic amination of bornane sultam-derived enolates with 1-chloro-1-nitrosocyclo hexane. Tetrahedron Lett. 31 (1990) 991-994.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 991-994
    • Oppolzer, W.1    Tamura, O.2
  • 6
    • 0346621023 scopus 로고
    • ε-Benzoylaminocaproic acid
    • J. C. Eck, C. S. Marvel. ε-Benzoylaminocaproic acid. Org. Syn. Coll. 2 (1943) 76-78
    • (1943) Org. Syn. Coll. , vol.2 , pp. 76-78
    • Eck, J.C.1    Marvel, C.S.2
  • 7
    • 0016618096 scopus 로고
    • Synthesis of nitrogen-15-labeled 2-substituted-2-thiazolines and analogous thiazines
    • J. Volford, D. Banfi. Synthesis of nitrogen-15-labeled 2-substituted-2-thiazolines and analogous thiazines. J. Lab. Comp. Radiopharm., 11 (1975) 419-426
    • (1975) J. Lab. Comp. Radiopharm. , vol.11 , pp. 419-426
    • Volford, J.1    Banfi, D.2
  • 8
    • 0017812205 scopus 로고
    • Convenient synthesis of some purine 8-5′-imino cyclonucleosides
    • T. Sasaki, K. Minamoto, H. Itoh. Convenient synthesis of some purine 8-5′-imino cyclonucleosides. J. Org. Chem. 43 (1978) 2320-2325
    • (1978) J. Org. Chem. , vol.43 , pp. 2320-2325
    • Sasaki, T.1    Minamoto, K.2    Itoh, H.3
  • 10
    • 0002619201 scopus 로고
    • A facile preparation of dialkyl carbonates from potassium carbonate and alkyl bromides by using organostannyl compound as a catalyst
    • T. Fujinami, S. Sato, S. Sakaï. A facile preparation of dialkyl carbonates from potassium carbonate and alkyl bromides by using organostannyl compound as a catalyst. Chem. Let. (1981) 749-752
    • (1981) Chem. Let. , pp. 749-752
    • Fujinami, T.1    Sato, S.2    Sakaï, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.