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  • Complete control of the chemoselectivity in catalytic carbene transfer reactions from ethyl diazoacetate: an N-heterocyclic carbene-Cu system that suppresses diazo coupling.

Complete control of the chemoselectivity in catalytic carbene transfer reactions from ethyl diazoacetate: an N-heterocyclic carbene-Cu system that suppresses diazo coupling.

Journal of the American Chemical Society (2004-09-02)
Manuel R Fructos, Tomás R Belderrain, M Carmen Nicasio, Steven P Nolan, Harneet Kaur, M Mar Díaz-Requejo, Pedro J Pérez
RESUMEN

The complex IPrCuCl (1) catalyzes the transfer of the :CHCO2Et group from ethyl diazoacetate (EDA) to unsaturated and saturated substrates (olefins, amine, alcohols) with very high yields. In the absence of substrate, the complex 1 does not react with EDA to give the diazo coupling products (fumarate and maleate), a rare example in the field of metal-catalyzed diazocompounds decomposition.

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Sigma-Aldrich
[1,3-Bis(2,6-diisopropylphenyl)-imidazol-2-ylidene]copper(I) chloride