Rhenium-catalyzed insertion of terminal alkenes into a C(sp(2))–H bond and successive transfer hydrogenation
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Treatment of aromatic aldimines with terminal alkenes in the presence of a rhenium catalyst, [HRe(CO)(4)](n), gives 2-alkenylbenzylamines in good to excellent yields. This reaction proceeds via the insertion of the alkene into a C-H bond at the ortho-position of the imino group of the aromatic aldimine followed by sequential beta-hydride elimination from the formed alkyl rhenium intermediate and then by hydrogenation of the imino group of the aldimine.
収録刊行物
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- Journal of Organometallic Chemistry
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Journal of Organometallic Chemistry 696 (1), 348-351, 2011-01-01
Elsevier Science SA.
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詳細情報 詳細情報について
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- CRID
- 1050846637416654976
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- NII論文ID
- 120003497018
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- NII書誌ID
- AA00704122
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- ISSN
- 0022328X
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- CiNii Articles