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Acta Chimica Sinica ›› 1990, Vol. 48 ›› Issue (5): 494-500. Previous Articles Next Articles
Original Articles
陈寿山;姚文庆
发布日期:
CHEN SHOUSHAN;YAO WENQING
Published:
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The steric effects on the reaction of 6,6-dialkylfulvene with organolithium have been studied. Reaction of EtLi with 6,6-dialkylfulvone readily results in the formation of reduction product. The addition products were formed by the reaction of BuLi with 6,6-dialkylfulvene. The analogous reaction of 6,6-polymethylenefulvene with organolithium was also examined Reaction of tetramethylenefulvene with aryllithium only leads to a-hydrogen elimination and in the case of penta and hexamethylenefulvene addition reaction takes place. A series of sec- and tert-alkyl and cycloalkenyl substituted titanocene and zirconocene derivatives have been prepared
Key words: CYCLOPENTADIENE P, PROTON MAGNETIC RESONANCE SPECTROMETRY, BARIUM COMPOUND, ALKENE P, TITANIUM COMPOUNDS, ZIRCONIUM COMPOUNDS
CLC Number:
O627
CHEN SHOUSHAN;YAO WENQING. Reaction of 6,6-dialkylfulvene with organolithium-syntheses of substituted titanocene and zirconocene derivatives[J]. Acta Chimica Sinica, 1990, 48(5): 494-500.
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