Artigo Revisado por pares

Carbene−Alkene Complexes between a Nucleophilic Carbene and Electron-Poor Alkenes

2008; American Chemical Society; Volume: 130; Issue: 44 Linguagem: Inglês

10.1021/ja8042118

ISSN

1943-2984

Autores

Jean‐Luc Mieusset, Michaël Abraham, Udo H. Brinker,

Tópico(s)

Catalytic C–H Functionalization Methods

Resumo

Spirooxadiazoline 5 is a clean thermal source of tricyclo[6.2.1.0 (2,7)]undec-9-en-11-ylidene (7), a typical foiled carbene. Species 7 can be trapped efficiently at 165 degrees C by electron-deficient alkenes like acrylonitrile and fumaronitrile whereby the anti addition products are obtained exclusively. Higher temperatures, however, favor intramolecular reactions. Density functional theory (DFT) calculations predict the formation of a strong complex between both reactants which actually is a minimum on the free energy scale. These results confirm the nucleophilic character of foiled carbenes and the presence of a significant barrier toward rearrangement.

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