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Volumn 45, Issue 43, 2004, Pages 8115-8117

Asymmetric epoxidation of cis-β-methylstyrenes catalyzed by N-aryl substituted oxazolidinone-containing ketones. A beneficial substituent effect

Author keywords

Asymmetric epoxidation; Chiral dioxirane; Chiral ketone; Phenyl phenyl interaction

Indexed keywords

ALKENE; KETONE DERIVATIVE; METHYL GROUP; OXAZOLIDINONE DERIVATIVE; PHENYL GROUP; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; STYRENE DERIVATIVE;

EID: 4644313101     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.124     Document Type: Article
Times cited : (49)

References (50)
  • 11
    • 6044269298 scopus 로고
    • For general leading references on dioxiranes see: R.W. Murray Chem. Rev. 89 1989 1187
    • (1989) Chem. Rev. , vol.89 , pp. 1187
    • Murray, R.W.1
  • 16
    • 0032975651 scopus 로고    scopus 로고
    • For recent reviews on chiral ketone catalyzed asymmetric epoxidation see: S.E. Denmark, and Z. Wu Synlett 1999 847
    • (1999) Synlett , pp. 847
    • Denmark, S.E.1    Wu, Z.2
  • 47
    • 4644300073 scopus 로고    scopus 로고
    • note
    • The epoxidation was carried out under more basic conditions as compared to the one described in Ref. 9. The conversion was improved under the current reaction condition
  • 48
    • 4644307962 scopus 로고    scopus 로고
    • note
    • The substituted cis-β-methylstyrenes were prepared by the Wittig olefination of substituted benzaldehydes and contained a mixture of cis- and trans-isomers


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.