Meerwein arylation
The Meerwein arylation is an organic reaction involving the addition of an aryl diazonium salt (ArN2X) to an electron-poor alkene usually supported by a metal salt. The reaction product is an alkylated arene compound. The reaction is named after Hans Meerwein, one of its inventors who first published it in 1939. In a general scope a Meerwein arylation is any reaction between an aryl radical and an alkene. The initial intermediate is an aryl enthenyl radical which can react with many trapping reagents such as hydrogen or halogens or with those based on nitrogen or sulfur.
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Meerwein arylation
The Meerwein arylation is an organic reaction involving the addition of an aryl diazonium salt (ArN2X) to an electron-poor alkene usually supported by a metal salt. The reaction product is an alkylated arene compound. The reaction is named after Hans Meerwein, one of its inventors who first published it in 1939. In a general scope a Meerwein arylation is any reaction between an aryl radical and an alkene. The initial intermediate is an aryl enthenyl radical which can react with many trapping reagents such as hydrogen or halogens or with those based on nitrogen or sulfur.
has abstract
Die Meerwein-Arylierung – auch ...... erstmals 1939 veröffentlicht.
@de
Meerwein芳基化反应（Meerwein arylati ...... 芳香族化合物。 烯烃上的吸电子基团降低了烯烃双键的电子密度。
@zh
The Meerwein arylation is an o ...... e based on nitrogen or sulfur.
@en
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name
Meerwein arylation
@en
namedafter
type
Coupling reaction
@en
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hypernym
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comment
Die Meerwein-Arylierung – auch ...... erstmals 1939 veröffentlicht.
@de
Meerwein芳基化反应（Meerwein arylati ...... 芳香族化合物。 烯烃上的吸电子基团降低了烯烃双键的电子密度。
@zh
The Meerwein arylation is an o ...... e based on nitrogen or sulfur.
@en
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Meerwein arylation
@en
Meerwein-Arylierung
@de
Meerwein芳基化反应
@zh