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Volumn 1, Issue 4, 1998, Pages 253-257

A convenient access to chiral and racemic (Z)-1-bromo-3-benzoxy-1-butene;(Z)-1-bromo-3-benzoxy-1-butène. Synthèse en séries racémique et chirale

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Indexed keywords


EID: 19244369154     PISSN: 13871609     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1387-1609(98)80043-1     Document Type: Article
Times cited : (1)

References (22)
  • 11
    • 85030036091 scopus 로고    scopus 로고
    • note
    • 1H-NMR analysis of the crude reaction mixture.
  • 12
    • 85030056958 scopus 로고    scopus 로고
    • At higher temperatures the stereochemical purity of the products was lower
    • [8] At higher temperatures the stereochemical purity of the products was lower.
  • 17
    • 85030050617 scopus 로고    scopus 로고
    • The enantiomeric excess were determined by chiral HPLC using a (R,R) WHELK 01 (Regis) chiral stationary phase (hexane/isopropanol). Chiral HPLC of the racemic mixtures gave two peaks of equal intensity
    • [13] The enantiomeric excess were determined by chiral HPLC using a (R,R) WHELK 01 (Regis) chiral stationary phase (hexane/isopropanol). Chiral HPLC of the racemic mixtures gave two peaks of equal intensity.
  • 20
    • 85030055580 scopus 로고    scopus 로고
    • Kieselgel 60 (R. Merck, 7734, 70-230 mesh) was used as the in situ absorbent in die oxidation reaction with PCC
    • [16] Kieselgel 60 (R. Merck, 7734, 70-230 mesh) was used as the in situ absorbent in die oxidation reaction with PCC.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.