3-Metallo substituted naphthalenes

Chemistry of carbon compounds – Miscellaneous organic carbon compounds – C-metal

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260396K, C07F 108

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active

041599934

ABSTRACT:
3-Prenyl-substituted menaquinones are made by reacting a 3-metallo-2-alkyl-1,4-di(alkoxy or aralkoxy) naphthalene with a prenyl halide, and then oxidizing the resulting 3-prenyl-2-alkyl-1,4-di(alkoxy or aralkoxy) naphthalene to prepare the corresponding 3-prenyl-substituted menaquinone. The metallo substituent at the 3-position may be Li, Li/Cu, Cu or MgBr. The oxidation is advantageously conducted by the use of argentic oxide.

REFERENCES:
patent: 3658863 (1972-04-01), Harrison
patent: 3798248 (1974-03-01), VAN Koten et al.
Coates et al., Organometallic Compounds, Methuen & Co. Ltd., London, vol. 2, 3rd Ed., pp. 253-254 (1968).
Chemical Abstracts, 31 1015.
Chemical Abstracts, 71 50163s (1969).
Camus et al., J. Organometallic Chem. 14, p. 441 (1968).

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