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Synlett 2017; 28(13): 1501-1509
DOI: 10.1055/s-0036-1588827
DOI: 10.1055/s-0036-1588827
synpacts
Lewis Acid Catalyzed Carbonyl–Olefin Metathesis
We thank the Petroleum Research Fund (PRF#54688-DNI1), the University of Michigan Office of Research, and the NIH/National Institute of General Medical Sciences (GM118644) for financial support. C.S.S. thanks the David and Lucile Packard Foundation. J.R.L. thanks the National Science Foundation for a predoctoral fellowship.Weitere Informationen
Publikationsverlauf
Received: 27. Februar 2017
Accepted after revision: 10. April 2017
Publikationsdatum:
16. Mai 2017 (online)
Abstract
Olefin–olefin metathesis has led to important advances in diverse fields of research, including synthetic chemistry, materials science, and chemical biology. The corresponding carbonyl–olefin metathesis also enables direct carbon–carbon bond formation from readily available precursors, however, currently available synthetic procedures are significantly less advanced. This Synpacts article provides an overview of recent achievements in the field of Lewis acid mediated and Lewis acid catalyzed carbonyl–olefin metathesis reactions.
1 Lewis Acid Mediated Carbonyl–Olefin Metathesis
2 Lewis Acid Catalyzed Carbonyl–Olefin Metathesis
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For metal-mediated carbonyl-olefin metathesis reactions, see:
For carbonyl–olefin metathesis reactions proceeding via oxetane photoadducts, see:
For catalytic carbonyl–olefin metathesis reactions proceeding via [3+2]/retro-[3+2] cycloaddition, see:
For the appliation of carbonyl–olefin metathesis in complex molecule synthesis, see: