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Volumn 133, Issue 20, 2011, Pages 7672-7675

Iron-catalyzed stereospecific activation of olefinic C-H bonds with grignard reagent for synthesis of substituted olefins

Author keywords

[No Author keywords available]

Indexed keywords

C-H BOND; CH-BOND ACTIVATION; COSOLVENTS; GRIGNARD REAGENT; STEREOSPECIFIC;

EID: 79957775911     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja2017202     Document Type: Article
Times cited : (140)

References (44)
  • 34
    • 79957744435 scopus 로고    scopus 로고
    • The reaction proceeded with comparable yield using various Fe(II) and Fe(III) salts having different purities. The presence of the iron catalyst and of the diamine ligand was mandatory. Without the oxidant, the reaction was stoichiometric in iron, and no reduction of the double bond was observed. See the Supporting Information for details
    • The reaction proceeded with comparable yield using various Fe(II) and Fe(III) salts having different purities. The presence of the iron catalyst and of the diamine ligand was mandatory. Without the oxidant, the reaction was stoichiometric in iron, and no reduction of the double bond was observed. See the Supporting Information for details.
  • 35
    • 79957787446 scopus 로고    scopus 로고
    • The amount of PhMgBr could be reduced to 2.4 equiv without an appreciable decrease in yield (73%)
    • The amount of PhMgBr could be reduced to 2.4 equiv without an appreciable decrease in yield (73%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.