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Volumn 357, Issue 5, 2015, Pages 1070-1078

Acid-catalyzed synthesis of α,β-disubstituted conjugated enones by a Meyer-Schuster-type rearrangement in allenols

Author keywords

alcohols; allenes; Br nsted acids; homogeneous catalysis; Lewis acids

Indexed keywords


EID: 84925047410     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400928     Document Type: Article
Times cited : (7)

References (63)
  • 5
    • 48549103913 scopus 로고    scopus 로고
    • (Eds.: R. Brückner, E. Schaumann), Georg Thieme Verlag, Stuttgart
    • I. Escher, F. Glorius, in: Science of Synthesis, Vol. 25, (Eds.:, R. Brückner, E. Schaumann,), Georg Thieme Verlag, Stuttgart, 2006, pp 733-777
    • (2006) Science of Synthesis , vol.25 , pp. 733-777
    • Escher, I.1    Glorius, F.2
  • 6
    • 48549103913 scopus 로고    scopus 로고
    • (Ed.: R. Bruckner), Georg Thieme Verlag, Stuttgart
    • E. F. Glorius, in: Science of Synthesis, Vol. 25, (Ed.:, R. Bruckner,), Georg Thieme Verlag, Stuttgart, 2007, p 733
    • (2007) Science of Synthesis , vol.25 , pp. 733
    • Glorius, E.F.1
  • 23
    • 0000467084 scopus 로고
    • S. S. Nikam, K. H. Chu, K. K. Wang, J. Org. Chem. 1986, 51, 745. The transformation of isoindolinone-linked alkoxyallenols into oxopropylidene isoindolinones has been reported by treatment with aqueous sulphuric acid
    • (1986) J. Org. Chem. , vol.51 , pp. 745
    • Nikam, S.S.1    Chu, K.H.2    Wang, K.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.