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Volumn , Issue 6, 2009, Pages 938-944

1,2-Diarylethanols by alternative regioselective reductive ring-opening of 2,3-diaryloxiranes

Author keywords

Alcohols; Enantioselectivity; Epoxides; Reduction; Regioselectivity; Ring opening reactions

Indexed keywords


EID: 60849130695     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200800992     Document Type: Article
Times cited : (19)

References (37)
  • 22
    • 60849123311 scopus 로고    scopus 로고
    • 1H NMR spectra with known compounds (2a, 2d, 2f, 2g, 3d and 3h) or by MS identification of characteristic fragments of type 5 for regioisomer 2 (2b and 2e) and of type 6 for regioisomer 3 (3b, 3e and 3f).
    • 1H NMR spectra with known compounds (2a, 2d, 2f, 2g, 3d and 3h) or by MS identification of characteristic fragments of type 5 for regioisomer 2 (2b and 2e) and of type 6 for regioisomer 3 (3b, 3e and 3f).
  • 33
    • 60849116019 scopus 로고    scopus 로고
    • 2 at room temp. gave an aldehyde of type 9 quantitatively.
    • 2 at room temp. gave an aldehyde of type 9 quantitatively.
  • 34
    • 60849108517 scopus 로고    scopus 로고
    • The ee values were measured by HPLC analysis using CHIRALCEL ODH as the chiral stationary phase (see Exp. Sect.).
    • The ee values were measured by HPLC analysis using CHIRALCEL ODH as the chiral stationary phase (see Exp. Sect.).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.