6533b828fe1ef96bd1288c7c
RESEARCH PRODUCT
An easy route to 1-germaindenes via a transmetallation zirconiumgermanium reaction
Jacques DubacPhilippe MeunierJean-claude DaranAli KanjBernard Gautheronsubject
Bicyclic moleculeTrimethylsilylOrganic ChemistryInorganic chemistryRegioselectivityMetallacycleBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundTransmetalationchemistryYield (chemistry)Materials ChemistryPhysical and Theoretical ChemistryGermanium tetrachlorideMetallocenedescription
Abstract Several 1-zirconaindenes ( 4 ) have been obtained easily by heating phenylmethylzirconocene with various symmetrical (R R′ CH 3 , C 2 H 5 , n-C 3 H 7 , Si(CH 3 ) 3 and unsymmetrical (R CH 3 , R′ Si(CH 3 ) 3 ) alkynes (RCCR′). Under similar experimental conditions, the ynamine, diethylaminotrimethylsilylethyne, led to a regioselective reaction. From the X-ray structure of the zirconaindene product, the trimethylsilyl group was found close to the zirconium atom. Compounds 4 with germanium tetrachloride afford new 1-germaindenes ( 7 ) characterized by 1 H and 13 C NMR and mass spectrometry, in good yield.
year | journal | country | edition | language |
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1993-07-01 | Journal of Organometallic Chemistry |