메뉴 건너뛰기




Volumn 663, Issue 1-2, 2002, Pages 21-31

Lithiophenylalkyllithiums: New dilithium reagents having both sp 2 - and sp 3 -hybridised remote carbanionic centres

Author keywords

Lithiation; Lithium compounds; Organolithium

Indexed keywords

ACID; ALKADIENE; ALKANONE; ALKYL GROUP; ANION; BENZALDEHYDE; BROMINE; BROMINE DERIVATIVE; CARBON; CARBONYL DERIVATIVE; CHLOROBENZENE; CYCLOHEXANONE; ETHER DERIVATIVE; LITHIUM; LITHIUM DERIVATIVE; NAPHTHALENE; OXEPANE DERIVATIVE; PHENYL GROUP; REAGENT; WATER;

EID: 0037011758     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(02)01473-0     Document Type: Article
Times cited : (14)

References (62)
  • 10
    • 0030496093 scopus 로고    scopus 로고
    • For reviews on arene-catalysed reductive lithiation processes
    • see
    • For reviews on arene-catalysed reductive lithiation processes, see: M. Yus, Chem. Soc. Rev. 25 (1996) 155
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 155
    • Yus, M.1
  • 14
    • 37049073704 scopus 로고
    • For the first account on this process from our laboratory
    • see
    • For the first account on this process from our laboratory, see: M. Yus, D.J. Ramón, J. Chem. Soc. Chem. Commun. (1991) 398.
    • (1991) J. Chem. Soc. Chem. Commun. , pp. 398
    • Yus, M.1    Ramón, D.J.2
  • 17
    • 0032510282 scopus 로고    scopus 로고
    • For a polymer supported version of this reaction
    • see: (a)
    • For a polymer supported version of this reaction, see: (a) C. Gómez, S. Ruiz, M. Yus, Tetrahedron Lett. 39 (1998) 1397
    • (1998) Tetrahedron Lett. , vol.39 , pp. 1397
    • Gómez, C.1    Ruiz, S.2    Yus, M.3
  • 20
    • 0012669991 scopus 로고    scopus 로고
    • Other many uses of this methodology are: (a) Preparation of functionalised organolithium compounds [12] by chlorine- lithium exchange or reductive opening of heterocyles [13]
    • Other many uses of this methodology are: (a) Preparation of functionalised organolithium compounds [12] by chlorine- lithium exchange or reductive opening of heterocyles [13]
  • 21
    • 0012733527 scopus 로고    scopus 로고
    • Generation of organolithium reagents starting from nonhalogenated materials [14]
    • Generation of organolithium reagents starting from nonhalogenated materials [14]
  • 22
    • 0012623649 scopus 로고    scopus 로고
    • Activation of other metals [15]
    • Activation of other metals [15]
  • 23
    • 0012672237 scopus 로고    scopus 로고
    • Transmetallation process 7d
    • Transmetallation process 7d.
  • 38
    • 0032742950 scopus 로고    scopus 로고
    • For related systems, see: and literature quoted therein
    • For related systems, see: J. Ortiz, A. Guijarro, M. Yus, Eur. J. Org. Chem. (1999) 3005 and literature quoted therein.
    • (1999) Eur. J. Org. Chem. , pp. 3005
    • Ortiz, J.1    Guijarro, A.2    Yus, M.3
  • 40
    • 33847797648 scopus 로고
    • For leading references on bromine-lithium exchange using an alkyllithium as lithiation agent
    • see: (a)
    • For leading references on bromine-lithium exchange using an alkyllithium as lithiation agent, see: (a) W.E. Parham, L.D. Jones, Y.A. Sayed, J. Org. Chem. 41 (1976) 1184
    • (1976) J. Org. Chem. , vol.41 , pp. 1184
    • Parham, W.E.1    Jones, L.D.2    Sayed, Y.A.3
  • 50
    • 0027168644 scopus 로고
    • For a related synthesis of oxepanes
    • see
    • For a related synthesis of oxepanes, see: J.F. Gil, D.J. Ramón, M. Yus, Tetrahedron 49 (1993) 4923.
    • (1993) Tetrahedron , vol.49 , pp. 4923
    • Gil, J.F.1    Ramón, D.J.2    Yus, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.