Efficient synthesis of ferrocenylcyclohexenone under solvent-free conditions

Zhi Liang Shen; Wei Juan Zhou; Jin Ming Yang; Shun Jun Ji

doi:10.1080/00397910902883553

Efficient synthesis of ferrocenylcyclohexenone under solvent-free conditions

Zhi Liang Shen, Wei Juan Zhou, Jin Ming Yang, Shun Jun Ji

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

Abstract

An efficient method for the synthesis of a series of ferrocenylcyclohexenones via tandem Michael-aldol reaction of ferrocenyl-substituted chalcones with dibenzyl ketone under solvent-free conditions is described. It was found that the factors including the electronic nature of chalcone, basicity of the base, reaction time, and temperature have effects on the formation of the ferrocenylcyclohexenones.

Original language	English
Pages (from-to)	3924-3933
Number of pages	10
Journal	Synthetic Communications
Volume	39
Issue number	21
DOIs	https://doi.org/10.1080/00397910902883553
State	Published - Jan 2009
Externally published	Yes

Keywords

Chalcone
Crystal structure
Cyclohexenone
Ferrocene
Solvent-free

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10.1080/00397910902883553

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abstract = "An efficient method for the synthesis of a series of ferrocenylcyclohexenones via tandem Michael-aldol reaction of ferrocenyl-substituted chalcones with dibenzyl ketone under solvent-free conditions is described. It was found that the factors including the electronic nature of chalcone, basicity of the base, reaction time, and temperature have effects on the formation of the ferrocenylcyclohexenones.",

keywords = "Chalcone, Crystal structure, Cyclohexenone, Ferrocene, Solvent-free",

author = "Shen, {Zhi Liang} and Zhou, {Wei Juan} and Yang, {Jin Ming} and Ji, {Shun Jun}",

year = "2009",

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AU - Shen, Zhi Liang

AU - Zhou, Wei Juan

AU - Yang, Jin Ming

AU - Ji, Shun Jun

PY - 2009/1

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N2 - An efficient method for the synthesis of a series of ferrocenylcyclohexenones via tandem Michael-aldol reaction of ferrocenyl-substituted chalcones with dibenzyl ketone under solvent-free conditions is described. It was found that the factors including the electronic nature of chalcone, basicity of the base, reaction time, and temperature have effects on the formation of the ferrocenylcyclohexenones.

AB - An efficient method for the synthesis of a series of ferrocenylcyclohexenones via tandem Michael-aldol reaction of ferrocenyl-substituted chalcones with dibenzyl ketone under solvent-free conditions is described. It was found that the factors including the electronic nature of chalcone, basicity of the base, reaction time, and temperature have effects on the formation of the ferrocenylcyclohexenones.

KW - Chalcone

KW - Crystal structure

KW - Cyclohexenone

KW - Ferrocene

KW - Solvent-free

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U2 - 10.1080/00397910902883553

DO - 10.1080/00397910902883553

M3 - 文章

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SN - 0039-7911

VL - 39

SP - 3924

EP - 3933

JO - Synthetic Communications

JF - Synthetic Communications

IS - 21

ER -

Efficient synthesis of ferrocenylcyclohexenone under solvent-free conditions

Abstract

Keywords

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