Intermolecular Hydroacylation by Transition‐Metal Complexes
書誌事項
- 公開日
- 2007-03-27
- 権利情報
-
- http://onlinelibrary.wiley.com/termsAndConditions#vor
- DOI
-
- 10.1002/ejoc.200600846
- 公開者
- Wiley
この論文をさがす
説明
<jats:title>Abstract</jats:title><jats:p>In this review, transition‐metal‐catalyzed intermolecular hydroacylation, which is a direct synthetic protocol generating ketones from aldehydes and unsaturated hydrocarbons, will be discussed. In order to avoid decarbonylation, one of the major side‐reactions occurring in transition‐metal‐catalyzed hydroacylation, several important strategies have been developed: An aldehyde ligand bearing a coordinating heteroatom at an appropriate position, a chelation auxiliary, and a masked form of the aldehyde, such as an aldimine or allylamine. Hydroacylation or its variations can also be applied to the synthesis of cycloalkanones and an α,β‐unsaturated ketone or to the carbon–carbon triple bond cleavage of an alkyne.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)</jats:p>
収録刊行物
-
- European Journal of Organic Chemistry
-
European Journal of Organic Chemistry 2007 (12), 1869-1881, 2007-03-27
Wiley