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Volumn 63, Issue 28, 2007, Pages 6625-6634

Selective lithiation of 1,6-dihalohex-1-enes and 1,6-dihalohex-1-ynes

Author keywords

Arene promoted lithiation; Dilithium synthons; Halogen lithium exchange; Lithium acetylides; Selective lithiation

Indexed keywords

ALCOHOL DERIVATIVE; ALKYNE DERIVATIVE; BENZALDEHYDE; BROMINE DERIVATIVE; CARBON; CHLORINE DERIVATIVE; HALOGEN; IODINE; LITHIUM DERIVATIVE; NAPHTHALENE DERIVATIVE; PENTANE; TETRAHYDROFURAN;

EID: 34249340860     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.03.106     Document Type: Article
Times cited : (4)

References (66)
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    • For a recent application of this stoichiometric lithiation reaction, see:. Deng K., Bensari-Bouguerra A., Whetstone J., and Cohen T. J. Org. Chem. 71 (2006) 2360
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    • For different examples from our group, see:
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    • These intermediates are functionalised organolithium compounds, which are very unstable species even at low temperatures that decompose either by elimination processes or by proton abstraction from the reaction medium. For reviews on this type of compounds, see:
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    • For a report on lithiation of bromo olefins (bromine-lithium exchange versus α-deprotonation) using t-BuLi, see:
    • For a report on lithiation of bromo olefins (bromine-lithium exchange versus α-deprotonation) using t-BuLi, see:. Bonnet B., Plé G., and Duhamel L. Synlett (1996) 221
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.