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Volumn 126, Issue 12, 2004, Pages 3686-3687

Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents

Author keywords

[No Author keywords available]

Indexed keywords

1 METHYL 2 PYRROLIDINONE; 1,4 DIAZABICYCLO[2.2.2]OCTANE; 4 METHYLMORPHOLINE; BROMINE DERIVATIVE; CHLORINE DERIVATIVE; CYCLOHEPTENE; DIAMINE; FUNCTIONAL GROUP; GRIGNARD REAGENT; HALIDE; IODINE DERIVATIVE; IRON; MONOAMINE; MORPHOLINE DERIVATIVE; N,N,N',N' TETRAMETHYLETHYLENEDIAMINE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; REAGENT; TRIETHYLAMINE; UNCLASSIFIED DRUG;

EID: 1642361256     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja049744t     Document Type: Article
Times cited : (452)

References (22)
  • 1
    • 0003393086 scopus 로고
    • Vereinigung Wissenschaftlicher Verleger: Berlin and Leipzig
    • Cf. Holleman, A. F. Lehrbuch der Organischen Chemie; Vereinigung Wissenschaftlicher Verleger: Berlin and Leipzig, 1920.
    • (1920) Lehrbuch der Organischen Chemie
    • Holleman, A.F.1
  • 10
    • 0037468071 scopus 로고    scopus 로고
    • (e) Terao, J.; Ikumi, A.; Kuniyasu, H.; Kambe, N. J. Am. Chem., Soc. 2003, 125, 5646-5647. A recent review see: Cárdenas, D. J. Angew. Chem., Int. Ed. 2003, 42, 384-387.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 384-387
    • Cárdenas, D.J.1
  • 20
    • 1642316677 scopus 로고    scopus 로고
    • note
    • 5) were not effective. See Supporting Information for details.
  • 22
    • 1642331165 scopus 로고    scopus 로고
    • note
    • The iron-catalyzed cross-coupling of 6-bromo-1-hexene with PhMgBr gave exclusively hex-5-enylbenzene (65%) under the slow-addition conditions at 25 °C. Under the conditions shown in eq 1 (at 25 °C), however, the product of a 5-exo-radical-cyclization/coupling process was obtained in 10% yield along with the formation of hex-5-enylbenzene (52%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.