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Volumn 694, Issue 22, 2009, Pages 3619-3625

Direct metalation of methoxymethyl arylmethyl ethers: A tin-free approach to the generation of α-alkoxyalkoxy-substituted aryllithiums

Author keywords

Acetals; Funtionalized organolithiums; Lithiation; Protecting groups; Regioselectivity

Indexed keywords

ACETALS; AROMATIC RINGS; BENZYLIC; FUNCTIONALIZED; FUNTIONALIZED ORGANOLITHIUMS; LITHIATION; METALATIONS; METHOXYMETHYL; ORGANOLITHIUM REAGENT; PROTECTING GROUPS; SIMPLE APPROACH;

EID: 69949083590     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2009.07.007     Document Type: Article
Times cited : (7)

References (28)
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    • For an alternative route to aryl α-methoxymethyl anions, see: and references therein
    • For an alternative route to aryl α-methoxymethyl anions, see:. Linderman R.J., Ghannam A., and Badejo I. J. Org. Chem. 56 (1991) 5213-5216 and references therein
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    • Metalation of benzylic alkoxides with alkyllithiums affords the corresponding ortho-metallated organometals. See:
    • Metalation of benzylic alkoxides with alkyllithiums affords the corresponding ortho-metallated organometals. See:. Meyer N., and Seebach D. D. Chem. Ber. 113 (1980) 1304-1319
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    • Protection of hydroxyl groups as methoxymethyl (MOM) ethers is widely employed in organic synthesis: P.J. Kocienski, P.J. Protecting Groups, third ed., Thieme Verlag, Stuttgart, 2005, pp. 286-295.
    • Protection of hydroxyl groups as methoxymethyl (MOM) ethers is widely employed in organic synthesis: P.J. Kocienski, P.J. Protecting Groups, third ed., Thieme Verlag, Stuttgart, 2005, pp. 286-295.
  • 23
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    • 2O as a solvent, led to lower conversions and/or formation of by products.
    • 2O as a solvent, led to lower conversions and/or formation of by products.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.