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Reaction of zirconocene dichloride with alkyllithiums or alkyl grignard reagents as a convenient method for generating a “zirconocene” equivalant and its use in zirconium-promoted cyclization of alkenes, alkynes, dienes, enynes, and diynes

Tetrahedron Letters · 1986 · Vol. 27(25) · pp. 2829–2832
Ei‐ichi NegishiFredrik CederbaumTamotsu Takahashi
Coordination Chemistry and OrganometallicsAsymmetric Synthesis and CatalysisSynthetic Organic Chemistry MethodsChemistryReagentZirconiumAlkylOrganic chemistryGrignard reagentMedicinal chemistryCombinatorial chemistry
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Reaction of zirconocene dichloride with alkyllithiums or alkyl grignard reagents as a convenient method for generating a “zirconocene” equivalant and its use in zirconium-promoted cyclization of alkenes, alkynes, dienes, enynes, and diynes · Scinovex