首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF ANNULATED 1,4-DIOXANES AND PERHYDRO-1,4- OXAZINES BY DOMINO-WACKER-CARBONYLATION AND DOMINO-WACKER-MIZOROKI-HECK REACTIONS
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SYNTHESIS OF ANNULATED 1,4-DIOXANES AND PERHYDRO-1,4- OXAZINES BY DOMINO-WACKER-CARBONYLATION AND DOMINO-WACKER-MIZOROKI-HECK REACTIONS

机译:多米诺-瓦克羰基化和多米诺-瓦克-咪唑基-赫克反应合成环状的1,4-二恶烷和PERHYDRO-1,4-恶嗪

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摘要

Palladium(II)-catalyzed domino reactions for the formation of 1,4-dioxanes and perhydro-1,4-oxazines starting from hydroxy alkenes are described. The domino-Wacker-carbonylation comprises a Wacker oxidation, subsequent CO-insertion and a nucleophilic substitution of the intermediately formed Pd-species. The domino-Wacker-Mizoroki-Heck reaction proceeds via a Wacker oxidation, subsequent insertion into the olefmic π-bond of α,β-unsatura-ted carbonyl compounds and β-hydride elimination.
机译:描述了钯(II)催化的多米诺反应,用于从羟基烯烃开始形成1,4-二恶烷和全氢-1,4-恶嗪。多米诺-瓦克羰基化包括瓦克氧化,随后的CO插入和中间形成的Pd物种的亲核取代。通过Wacker氧化进行多米诺-Wacker-Mizoroki-Heck反应,随后将α,β-不饱和羰基化合物插入到烯烃的π键中,并消除了β-氢化物。

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