2017
DOI: 10.1055/s-0036-1589142
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A Practical Three-Step Synthesis of Vinylferrocene

Abstract: An improved, short and efficient synthesis of vinylferrocene is reported. This three-step synthesis includes Friedel–Crafts acylation, reduction, and a one-pot mesylation/elimination step to afford the target compound in 62% yield over three steps.

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Cited by 9 publications
(2 citation statements)
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“…Vinylferrocene was prepared from ferrocene according to an efficient three‐step protocol reported by Šebesta and co‐workers [24] . All other reagents used in this work were of the best commercial grade available and used without further purification.…”
Section: Methodsmentioning
confidence: 99%
“…Vinylferrocene was prepared from ferrocene according to an efficient three‐step protocol reported by Šebesta and co‐workers [24] . All other reagents used in this work were of the best commercial grade available and used without further purification.…”
Section: Methodsmentioning
confidence: 99%
“…Octamethylcyclotetrasiloxane (D 4 , 98%), 1,3,5,7-tetramethylcyclotetrasiloxane (H 4 D 4 , 98%), 1,1,3,3-tetramethyl-1,3-divinyldisiloxane (98%), 1,3,3,5,5,7,7-heptamethylcyclotetrasiloxane (HD 4 , 95%), and platinum (0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex 0.1 M solution in xylene were purchased from Abcr GmbH (Karlsruhe, Germany) and utilized as received. Vinylferrocene was synthesized from ferrocene (98%, Shanghai Macklin Biochemical Co., Shanghai, China) according to the known three-step procedures [54,66]. Previously described substances were analyzed by nuclear magnetic resonance (NMR) spectroscopy before being used.…”
Section: Methodsmentioning
confidence: 99%