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In the McMurry reaction, alkenes are synthesized by the reductive coupling of aldehydes and ketones using low valent titanium reagents. This reaction can be thought of as the opposite transformation to ozonolysis. There are many efficient intramolecular examples, including applications to the synthesis of macrocycles and various natural products.
・Tyrlik, S.; Wolochowicz, I. Bull. Soc. Chim. Fr. 1973, 2147
・Mukaiyama, T. et al. Chem. Lett. 1973, 1041. doi:10.1246/cl.1973.1041
・McMurry, J. E.; Fleming, M. P. J. Am. Chem. Soc. 1974, 96, 4708. DOI:10.1021/ja00821a076
・McMurry, J. E. Chem. Rev. 1989, 89, 1513. DOI: 10.1021/cr00097a007
・Robertson, G. M. Comp. Org. Syn. 1991, 3, 583.
・Furstner, A.; Jumbam, D. N. Tetrahedron 1992, 48, 5991. doi:10.1016/S0040-4020(01)89848-3
・Lipski, T. A.; Hilfiker, M. A.; Nelson, G. A. J. Org. Chem. 1997, 62, 4566. DOI: 10.1021/jo970792o
The in situ-formed low valent titanium species works as the active reagent. The reaction goes through the pinacol coupling-type intermediates and the driving force is the strong O-Ti bond. The reaction can be stopped at the pinacol intermediates if carried out at low temperature.
The synthesis of 13-hydroxynecembrane.
The McMurry coupling was one of the key steps in the total synthesis of taxol.