Kinetics and mechanism of the alkyl and aryl elimination from .eta.5-cyclopentadienylalkyl(and -aryl)dicarbonyliron(II) complexes initiated by mercury(II) halides-Reference-Cited by-同舟云学术

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Kinetics and mechanism of the alkyl and aryl elimination from .eta.5-cyclopentadienylalkyl(and -aryl)dicarbonyliron(II) complexes initiated by mercury(II) halides

Published:1977-08 Issue:16 Volume:99 Page:5295-5303
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Dizikes Louis J.,Wojcicki Andrew

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00458a012

Cited by 42 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Arylation of styrene derivatives using aryliron complexes [CpFe(CO)2Ar] revealed by density functional theory calculations: Fe(II)-assisted group exchange through Fe–C bond cleavage and Fe–X bond formation;Journal of Organometallic Chemistry;2011-12

3. (Cyclopentadienyl)dicarbonylmethyliron ((η5-C5H5)Fe(CO)2CH3, FpMe), a Seminal Transition-Metal Alkyl Complex: Mobility of the Methyl Group;Organometallics;2010-06-10

4. Arylation of Styrenes with Aryliron Complexes [CpFe(CO)2Ar];Organometallics;2010-05-12

5. Use of Aryliron Complexes [CpFe(CO)2Ar] as Arylcarbonyl Cation Equivalents in the Reactions with Organolithium Reagents To Yield Ketones;Organometallics;2009-07-30

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