The Use of Liquid Phase Oxidation for the Preparation of Nuclearly Substituted Styrenes. II. p-Vinylphenyl Acetate

Emerson, William S.; Heyd, J.W.; Lucas, Victor E.; Cook, William B.; Owens, Grafton R.; Shortridge, Robert W.

doi:10.1021/ja01212a508

Cited by 9 publications

(4 citation statements)

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“…Electrophilic acylation of phenol followed by reduction and dehydration was employed in the commercial production of p-vinylphenol by Maruzen Petrochemicals Co 3 . Another method that utilized benzylic oxidation of ethylphenol was reported 4 . Halophenol derivatives could be vinylated by the Heck reaction 5 .…”

Section: Introductionmentioning

confidence: 99%

Tributylphosphine as an Efficient Catalyst in C-Vinylation of Naphthol Derivatives

Hassanabadi¹,

Mosslemin²,

Rasolhosseini³

2013

Chem Sci Trans

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Section: Introductionmentioning

confidence: 99%

Tributylphosphine as an Efficient Catalyst in C-Vinylation of Naphthol Derivatives

Hassanabadi¹,

Mosslemin²,

Rasolhosseini³

2013

Chem Sci Trans

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“…Electrophilic acylation of phenol followed by reduction and dehydration was employed in the commercial production of p-vinylphenol by Maruzen Petrochemicals Co. 2,3 Another method which utilized benzylic oxidation of ethylphenol was reported. 4 Halophenol derivatives could be vinylated by the Heck reaction. 5 Yamaguchi 6 -9 reported the ethenylation reaction of phenol using the SnCl 4 -Bu 3 N reagent system.…”

Section: Introductionmentioning

confidence: 99%

Studies on the reaction of organotin phenoxides with ethyl propiolate catalysed by triethylamine and tin(IV) chloride

Kinart

2007

Applied Organom Chemis

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Different tributyltin phenoxides react at room temperature with ethyl propiolate in benzene, in the presence of tin(IV) chloride, triethylamine and their mixture to give the derivatives of 3-phenoxyacrylic acid ethyl ester. Exceptionally, 3-(2-hydroxyphenyl)acrylic acid ethyl ester and 3-(2-hydroxy-5-methylphenyl)acrylic acid ethyl ester have been obtained from the reaction of tributylphenoxytin and tributyl(p-tolyloxy)tin, respectively catalysed by SnCl 4 , and they have been easily hydrolysed to coumarin and 6-methylcoumarin.

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“…Electrophilic acylation of phenol followed by reduction and dehydration was employed in the commercial production of p-vinylphenol by Maruzen Petrochemicals Co. 2,3 Another method which utilized benzylic oxidation of ethylphenol was reported. 4 Halophenol derivatives could be vinylated by the Heck reaction. 5 reported the ethenylation reaction of phenol using the SnCl 4 -Bu 3 N reagent system.…”

Section: Introductionmentioning

confidence: 99%

Studies on the catalysis of the reaction of organotin phenoxides with diethyl acetylenedicarboxylate

Kinart¹,

Kinart²,

Trần³

et al. 2005

Appl. Organometal. Chem.

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The Use of Liquid Phase Oxidation for the Preparation of Nuclearly Substituted Styrenes. II. p-Vinylphenyl Acetate

Cited by 9 publications

References 0 publications

Tributylphosphine as an Efficient Catalyst in C-Vinylation of Naphthol Derivatives

Tributylphosphine as an Efficient Catalyst in C-Vinylation of Naphthol Derivatives

Studies on the reaction of organotin phenoxides with ethyl propiolate catalysed by triethylamine and tin(IV) chloride

Studies on the catalysis of the reaction of organotin phenoxides with diethyl acetylenedicarboxylate

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