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Volumn 17, Issue 2, 2015, Pages 282-285

Oxidative umpolung α-alkylation of ketones

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EID: 84921315267     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol503384c     Document Type: Article
Times cited : (43)

References (47)
  • 8
    • 84855305601 scopus 로고    scopus 로고
    • For an elegant three-step one-pot procedure for α-arylation and alkylation of ketones involving enamine formation using isoxazolidine (2 equiv) and alkylation with an organoaluminium reagent (2 equiv), see: Miyoshi, T.; Miyakawa, T.; Ueda, A.; Miyata, O. Angew. Chem. 2011, 123, 958
    • (2011) Angew. Chem. , vol.123 , pp. 958
    • Miyoshi, T.1    Miyakawa, T.2    Ueda, A.3    Miyata, O.4
  • 10
    • 84903499580 scopus 로고    scopus 로고
    • Oxidative Functionalization with Hypervalent Halides. In, 2 nd ed. Molander, G. A. Knochel, P. Elsevier: Oxford
    • Singh, F. V.; Wirth, T. Oxidative Functionalization with Hypervalent Halides. In Comprehensive Organic Synthesis, 2 nd ed.; Molander, G. A.; Knochel, P., Eds.; Elsevier: Oxford; 2014; Vol. 7, p 880.
    • (2014) Comprehensive Organic Synthesis , vol.7 , pp. 880
    • Singh, F.V.1    Wirth, T.2
  • 12
    • 84901748878 scopus 로고    scopus 로고
    • For a recent example of TMS-enolether dimerization, C-O and C-N bond formation through umpolung, see
    • For a recent example of TMS-enolether dimerization, C-O and C-N bond formation through umpolung, see: Mizar, P.; Wirth, T. Angew. Chem., Int. Ed. 2014, 53, 5993
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 5993
    • Mizar, P.1    Wirth, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.