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Volumn , Issue 6, 2011, Pages 1106-1112

Stereoselective total synthesis of (+)-nephrosteranic acid and (+)-roccellaric acid through asymmetric dihydroxylation and Johnson-Claisen rearrangement

Author keywords

Asymmetric synthesis; Diastereoselectivity; Dihydroxylation; Rearrangement; Total synthesis

Indexed keywords


EID: 79851481716     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001419     Document Type: Article
Times cited : (34)

References (42)
  • 1
    • 79851472912 scopus 로고    scopus 로고
    • Isolation
    • Isolation
  • 15
    • 79851473893 scopus 로고    scopus 로고
    • Isolation
    • Isolation
  • 16
    • 0009622717 scopus 로고
    • synthesis
    • O. Hesse, J. Prakt. Chem. 1898, 57, 232-318, synthesis
    • (1898) J. Prakt. Chem. , vol.57 , pp. 232-318
    • Hesse, O.1
  • 32
    • 79851470907 scopus 로고    scopus 로고
    • For similar regioselective asymmetric dihydroxylation of distant olefinic bond of a α,β,γ,δ-unsaturated esters, see
    • For similar regioselective asymmetric dihydroxylation of distant olefinic bond of a α,β,γ,δ-unsaturated esters, see
  • 37
    • 79851483436 scopus 로고    scopus 로고
    • Enantiomeric excess was determined by chiral HPLC
    • Enantiomeric excess was determined by chiral HPLC.
  • 38
    • 79851472519 scopus 로고    scopus 로고
    • For the Johnson-Claisen rearrangement, see
    • For the Johnson-Claisen rearrangement, see
  • 39
  • 42
    • 79851470304 scopus 로고    scopus 로고
    • 1H NMR spectroscopic analysis of the mixture
    • 1H NMR spectroscopic analysis of the mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.