메뉴 건너뛰기




Volumn 38, Issue 13, 1997, Pages 2227-2230

Facile hydrolysis and formation of amide bonds by N-hydroxyethylation of α-amino acids

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE;

EID: 0031592559     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00330-4     Document Type: Article
Times cited : (21)

References (19)
  • 9
    • 84920295845 scopus 로고    scopus 로고
    • note
    • 2O-phosphate buffer, the intermediency of lactone 2 was shown by transient build up and decay of its spectrum, which exhibits triplets at δ= 4.35, 3.65, 2.85 and 2.55 and a singlet at 3.40.
  • 10
    • 84920300584 scopus 로고
    • 10. Knorr, E. Ann. 1899, 307, 199-206.
    • (1899) Ann. , vol.307 , pp. 199-206
    • Knorr, E.1
  • 11
    • 84920295844 scopus 로고    scopus 로고
    • note
    • 19 and the hydrochloride of the amino acid amide in methanol. Triethylamine was added dropwise until the solution was clear, the reaction was allowed to stir overnight, and the product isolated by column chromatography. All new compounds gave confirmatory NMR, IR and high resolution mass spectral data.
  • 15
    • 0028857547 scopus 로고
    • 15. Duggleby, H. J. et al. Nature 1995, 373, 264-268.
    • (1995) Nature , vol.373 , pp. 264-268
    • Duggleby, H.J.1
  • 18
    • 0026785263 scopus 로고
    • 18. Walker, V. E. et al. Cancer Res. 1992, 52, 4320-4327.
    • (1992) Cancer Res. , vol.52 , pp. 4320-4327
    • Walker, V.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.