Organometallics · 2003 · 12 citations · 14 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisReaction IntermediatesReaction MechanismsHeterocyclic ReactivityKetones
Herein we report the CH insertion of a stable germylene, Ge[CH(SiMe 3 ) 2 ] 2, into the α - CH bonds of the acetyl-containing ketones acetone, butanone, and cyclopropyl methyl ketone. This CH insertion reaction requires the presence of MgCl 2, yet the reaction can be successfully carried out in hydrocarbon, aromatic, and ethereal solvents. In the absence of MgCl 2, these acetyl-containing ketones do not undergo CH insertion but instead undergo an OH insertion to give a germyl vinyl ether. A number of other ketones, including the acetyl-containing pinacolone, have been observed to only undergo insertion into the OH bond even in the presence of MgCl 2 .
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The manipulation of air-sensitive compounds
Janice Smith · Journal of Organometallic Chemistry · 1987 · 1.4K citations
Paul R. Blake, Jae B. Park, Michael W. W. Adams et al. · Journal of the American Chemical Society · 1992 · 112 citations