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Volumn 10, Issue 1, 2012, Pages 56-59

Synthesis of enantioenriched γ-quaternary cycloheptenones using a combined allylic alkylation/Stork-Danheiser approach: Preparation of mono-, bi-, and tricyclic systems

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLIC ALKYLATION; GENERAL METHOD; NATURAL PRODUCTS; QUATERNARY STEREOCENTERS; QUENCHING PARAMETERS; SEVEN-MEMBERED RINGS; TRICYCLIC COMPOUNDS;

EID: 82955163945     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06189e     Document Type: Article
Times cited : (30)

References (29)
  • 23
    • 61449196774 scopus 로고    scopus 로고
    • Concurrent with our efforts, palladium-catalyzed asymmetric allylic alkylations to form enantioenriched α-quaternary vinylogous esters and thioesters have also been performed by Trost. See
    • K. V. Petrova J. T. Mohr B. M. Stoltz Org. Lett. 2009 11 293
    • (2009) Org. Lett. , vol.11 , pp. 293
    • Petrova, K.V.1    Mohr, J.T.2    Stoltz, B.M.3
  • 28
    • 33947084958 scopus 로고
    • 1H NMR study. See Supporting Information trans-Propenyl analog 18 is prepared by palladium-catalyzed isomerization of terminal olefin 9. See ref. 2d for details
    • G. Stork R. L. Danheiser J. Org. Chem. 1973 38 1775
    • (1973) J. Org. Chem. , vol.38 , pp. 1775
    • Stork, G.1    Danheiser, R.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.