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Volumn 80, Issue 11, 2015, Pages 5870-5876

Halogenative difluorohomologation of ketones

Author keywords

[No Author keywords available]

Indexed keywords

HALOGENATION; REACTION INTERMEDIATES;

EID: 84930679733     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.5b00904     Document Type: Article
Times cited : (51)

References (58)
  • 36
    • 84930656896 scopus 로고    scopus 로고
    • The stability of compounds 2 depends on their structure. Cyclopropanes 2 derived from acetophenones are sensitive even to aqueous workup, while cyclopropanes 2 derived from cyclic ketones can be distilled under vacuum.
    • The stability of compounds 2 depends on their structure. Cyclopropanes 2 derived from acetophenones are sensitive even to aqueous workup, while cyclopropanes 2 derived from cyclic ketones can be distilled under vacuum.
  • 37
    • 0000545774 scopus 로고
    • For similar instability of difluorinated cyclopropanols generated under basic conditions, see
    • For similar instability of difluorinated cyclopropanols generated under basic conditions, see: Crabbe, P.; Cervantes, A.; Cruz, A.; Galeazzi, E.; Iriarte, J.; Velarde, E. J. Am. Chem. Soc. 1973, 95, 6655-6665
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 6655-6665
    • Crabbe, P.1    Cervantes, A.2    Cruz, A.3    Galeazzi, E.4    Iriarte, J.5    Velarde, E.6
  • 39
  • 53
    • 84893863008 scopus 로고    scopus 로고
    • The exchange of halogen X between Me3SiCF2X and halide ion (X = Cl, Br) was described; see
    • The exchange of halogen X between Me3SiCF2X and halide ion (X = Cl, Br) was described; see: Wang, F.; Li, L.; Ni, C.; Hu, J. Beilstein J. Org. Chem. 2014, 10, 344-351
    • (2014) Beilstein J. Org. Chem. , vol.10 , pp. 344-351
    • Wang, F.1    Li, L.2    Ni, C.3    Hu, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.