Gold‐Catalyzed Intermolecular Anti‐Markovnikov Hydroamination of Alkylidenecyclopropanes
抄録
<jats:title>Abstract</jats:title><jats:p>The cationic gold phosphine complex [{PCy<jats:sub>2</jats:sub>(<jats:italic>o</jats:italic>‐biphenyl)}Au(NCMe)]<jats:sup>+</jats:sup>SbF<jats:sub>6</jats:sub><jats:sup>−</jats:sup> (Cy=cyclohexyl) catalyzes the intermolecular, anti‐Markovnikov hydroamination reaction of monosubstituted and <jats:italic>cis</jats:italic>‐ and <jats:italic>trans</jats:italic>‐disubstituted alkylidenecyclopropanes (ACPs) with imidazolidin‐2‐ones and other nucleophiles. This reaction forms 1‐cyclopropyl alkylamine derivatives in high yield and with high regio‐ and diastereoselectivity. NMR spectroscopic analysis of gold π‐ACP complexes and control experiments point to the sp hybridization of the ACP internal alkene carbon atom as controlling the regiochemistry of the ACP hydroamination reaction.</jats:p>
収録刊行物
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- Angewandte Chemie International Edition
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Angewandte Chemie International Edition 54 (7), 2251-2254, 2014-12-22
Wiley
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キーワード
詳細情報 詳細情報について
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- CRID
- 1363670321012301440
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- ISSN
- 15213773
- 14337851
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- データソース種別
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- Crossref