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Volumn 9783527333431, Issue , 2014, Pages 351-374

Reductive Lithiation and Multilithiated Compounds in Synthesis

Author keywords

Electron transfer; Multilithiated compounds; Organolithium; Reductive lithiation

Indexed keywords

ELECTRON TRANSFER; FUNCTIONALIZED; LITHIATION; METALATIONS; MULTILITHIATED COMPOUND; ORGANIC SYNTHESIS; ORGANOLITHIUM REAGENT; ORGANOLITHIUMS; REACTION CONDITIONS; REDUCTIVE LITHIATION;

EID: 84927030900     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527667512.ch12     Document Type: Chapter
Times cited : (6)

References (91)
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    • 33646944179 scopus 로고    scopus 로고
    • For a critical comparison between the employment of PAH radical anions under stoichiometric and catalytic reaction conditions, see, and references therein.
    • For a critical comparison between the employment of PAH radical anions under stoichiometric and catalytic reaction conditions, see: Yang, A., Butela, H., Deng, K., Doubleday, M.D., and Cohen, T. (2006) Tetrahedron, 62, 6526, and references therein.
    • (2006) Tetrahedron , vol.62 , pp. 6526
    • Yang, A.1    Butela, H.2    Deng, K.3    Doubleday, M.D.4    Cohen, T.5
  • 13
  • 14
    • 0033979918 scopus 로고    scopus 로고
    • For a selection of recent reviews on the reductive lithiation and related topics, see
    • For a selection of recent reviews on the reductive lithiation and related topics, see: Ramon, D.J. and Yus, M. (2000) Eur. J. Org. Chem., 225;
    • (2000) Eur. J. Org. Chem. , pp. 225
    • Ramon, D.J.1    Yus, M.2
  • 15
    • 40749138993 scopus 로고    scopus 로고
    • (eds O.A. Attanasi and D. Spinelli), Italian Society of Chemistry, Rome
    • Yus, M. and Foubelo, F. (2002) in Targets in Heterocyclic Systems, Vol. 6 (eds O.A. Attanasi and D. Spinelli), Italian Society of Chemistry, Rome, p. 136;
    • (2002) Targets in Heterocyclic Systems , vol.6 , pp. 136
    • Yus, M.1    Foubelo, F.2
  • 16
    • 85192411446 scopus 로고    scopus 로고
    • Tetrahedron Organic Chemistry Series, Elsevier, B. V., Amsterdam, Chapter 4
    • Clayden, J. (2002) Organolithiums: Selectivity for Synthesis, Tetrahedron Organic Chemistry Series, Elsevier, B. V., Amsterdam, Vol. 23, Chapter 4, p. 149;
    • (2002) Organolithiums: Selectivity for Synthesis , vol.23 , pp. 149
    • Clayden, J.1
  • 17
    • 0037503118 scopus 로고    scopus 로고
    • (eds Z. Rapopport and I. Marek), Part 2, John Wiley & Sons, Ltd, Chichester
    • Yus, M. (2003) in The Chemistry of Organolithium Compounds (eds Z. Rapopport and I. Marek), Part 2, John Wiley & Sons, Ltd, Chichester, p. 647;
    • (2003) The Chemistry of Organolithium Compounds , pp. 647
    • Yus, M.1
  • 60
    • 0003791302 scopus 로고    scopus 로고
    • 4th, Part B edn, Kluwer Academic/Plenum Publishers, New York
    • Carey, F.A. and Sundberg, R.J. (2001) Advanced Organic Chemistry, 4th, Part B edn, Kluwer Academic/Plenum Publishers, New York, p. 293.
    • (2001) Advanced Organic Chemistry , pp. 293
    • Carey, F.A.1    Sundberg, R.J.2
  • 76
    • 79951621790 scopus 로고    scopus 로고
    • It was later demonstrated that replacement of the diphenylsilane motif by a more labile diarylsilane moiety allows the selective hydrolysis of one or two aryl groups by treatment with TFA
    • It was later demonstrated that replacement of the diphenylsilane motif by a more labile diarylsilane moiety allows the selective hydrolysis of one or two aryl groups by treatment with TFA:Hernández, D., Mose, R., and Skrydstrup, T. (2011) Org. Lett., 13, 732.
    • (2011) Org. Lett. , vol.13 , pp. 732
    • Hernández, D.1    Mose, R.2    Skrydstrup, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.