CO Insertion Reaction of Zirconacyclopentadienes.
β Scribed by Zhenfeng Xi; Hong-Tao Fan; Shizue Mito; Tamotsu Takahashi
- Book ID
- 101957137
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 172 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Reactions of organo-metal compounds O 0350 CO Insertion Reaction of Zirconacyclopentadienes. -Alkyl-substituted zirconacyclopentadienes react with CO directly at room temperature to give cyclopentenone derivatives as mixtures of trans/cis isomers after hydrolysis. Cyclopentadienones are not formed. If zirconaindene (V) is treated under these conditions, both indanones and indenones are obtained. A mixture of double bond isomers is derived from unsymmetrical zirconacyclopentadiene (IX). -(XI*, Z.
π SIMILAR VOLUMES
Copper-mediated reaction of zirconacyclopentadienes with iodopropenoates afforded pentaand hexasubstituted cyclopentadienes.