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Volumn 45, Issue 27, 2004, Pages 5279-5282

Elaboration of a novel effective approach to enantiopure functionalised 2,2′-dialkyl-1,1′-binaphthyls by stereoconservative cross-couplings at positions 2 and 2′

Author keywords

Aryl iodide; Aryl triflate; Binaphthyl; Cross coupling; Kumada; Negishi; Stereoconservative

Indexed keywords

IODINE DERIVATIVE; NAPHTHYL GROUP; ORGANOMETALLIC COMPOUND; TRIFLUOROMETHANESULFONIC ACID;

EID: 2942685126     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.05.016     Document Type: Article
Times cited : (10)

References (41)
  • 11
    • 0042880949 scopus 로고    scopus 로고
    • and references cited therein
    • Maruoka K., Ooi T. Chem. Rev. 103:2003;3013-3028. and references cited therein
    • (2003) Chem. Rev. , vol.103 , pp. 3013-3028
    • Maruoka, K.1    Ooi, T.2
  • 39
    • 0032742638 scopus 로고    scopus 로고
    • and references cited therein
    • Putala M. Enantiomer. 4:1999;243-262. and references cited therein
    • (1999) Enantiomer , vol.4 , pp. 243-262
    • Putala, M.1
  • 41
    • 2942677708 scopus 로고    scopus 로고
    • 4andthesolventwasremovedinvacuo. Theproductwasisolatedbyflashchromatographyonsilica,usinghexaneorhexane- dichloromethanefrom9:1upto4:1aseluents
    • 4 and the solvent was removed in vacuo. The product was isolated by flash chromatography on silica, using hexane or hexane-dichloromethane from 9:1 up to 4:1 as eluents.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.