Journal of the American Chemical Society · 1999 · 63 citations · 29 references
Natural SciencesBiochemistryChemistryBiocatalysisEnzymologyOrganic ChemistryCoenzyme ChemistryCross-coupling ReactionsOrganic SynthesisCoenzyme AnaloguesCoenzyme StructureQuinone ChemistryQuinone FormationUbiquinone BiosynthesisUbiquinone Chemistry
Syntheses of coenzyme Q 3 - 8 are described, as well as related systems such as plastoquinone-5. Preparation of the higher homologues of the ubiquinones relies on two new conjunctive reagents, or “linchpins”, each of which ultimately corresponds to two or three prenyl units. These allow for attachment of a polyprenyl halide at one end, followed by a Ni(0)-catalyzed cross-coupling at the other terminus with a chloromethylated p -quinone.
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Kohei Tamao, Koji Sumitani, Yoshihisa Kiso et al. · Bulletin of the Chemical Society of Japan · 1976 · 589 citations · Full text
David E. Van Horn, Ei‐ichi Negishi · Journal of the American Chemical Society · 1978 · 284 citations