Ruthenium allenylidene/alkenylcarbyne complexes triggering keto-enol tautomerism:: An alternative approach to γ-keto vinylidenes from simple ketones and 1,3-dicarbonyl compounds

被引：23

作者：

Bustelo, Emilio ^{[1
]}

Jimenez-Tenorio, Manuel ^{[1
]}

Puerta, M. Carmen ^{[1
]}

Valerga, Pedro ^{[1
]}

机构：

[1] Univ Cadiz, Fac Ciencias, Dept Ciencia Mat & Ingn Met & Quim Inorgan, E-11510 Puerto Real, Spain

来源：

ORGANOMETALLICS | 2006年 / 25卷 / 16期

关键词：

D O I：

10.1021/om060453y

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

[Cp*Ru(=C=C=CHPh)(dippe)][BF4] and [Cp*Ru(equivalent to C-C=CHPh)(dippe)][BF4](2) complexes are reactive toward a variety of simple ketones (acetone, acetophenone, cyclopentanone) and 1,3-dicarbonyl compounds ( acetylacetone, dimethylmalonate, malononitrile, ethyl acetoacetate) to give a series of alkylated vinylidene compounds [Cp*Ru{=C=CH-CH(L)Ph}(dippe)][BF4] (dippe = 1,2-bis(diisopropylphosphino) ethane). Two cross-linked processes are operating simultaneously, creating two interconverting pairs of species: the allenylidene/carbyne complexes and the keto/enol tautomers of the ketones, producing the final vinylidene product, which is stable due to the formation of a new C-C bond. The protonation/deprotonation equilibrium produces the electrophilic alkenylcarbyne complex and enols as the nucleophilic reagent. Stoichiometric studies with deuterated reagents and NMR monitoring of the reaction have been carried out. The X-ray structure of [Cp*Ru{=C=CH-CH(CH2COCH3)Ph}(dippe)][BF4] is also reported.

引用

页码：4019 / 4025

页数：7

共 59 条

[51] Preparation of dicationic chalcogenolate-bridged diruthenium complexes and their dual catalytic activity toward reactions between propargylic alcohols and acetone [J].