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Volumn 39, Issue 16, 1998, Pages 2269-2272

Unexpected 1,3-oxazolidine formation in the attempted oxidation of N- aryl-N-methyl substituted β-amino alcohols using pyridinium dichromate

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; OXAZOLIDINE DERIVATIVE; PYRIDINIUM DERIVATIVE;

EID: 0032537150     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00289-5     Document Type: Article
Times cited : (25)

References (21)
  • 3
    • 0010689952 scopus 로고    scopus 로고
    • 13C NMR, LSIMS and HRMS) consistent with assigned structures have been obtained for all new compounds. Yields refer to chromatographically and spectroscopically homogeneous material and are unoptimized
    • 13C NMR, LSIMS and HRMS) consistent with assigned structures have been obtained for all new compounds. Yields refer to chromatographically and spectroscopically homogeneous material and are unoptimized
  • 10
    • 0010733155 scopus 로고    scopus 로고
    • 2 at 0 °C, for 5 h in a 93 % yield
    • 2 at 0 °C, for 5 h in a 93 % yield.
  • 12
    • 0010689797 scopus 로고    scopus 로고
    • note
    • +).
  • 13
    • 0010732908 scopus 로고    scopus 로고
    • 13C NMR spectra and DEPT-135 spectrum were recorded. Taken together, these NMR experiments provided the evidence for the assigned N-aryl-1,3-oxazolidine structures
    • 13C NMR spectra and DEPT-135 spectrum were recorded. Taken together, these NMR experiments provided the evidence for the assigned N-aryl-1,3-oxazolidine structures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.