Yang L.-L,
Evans D,
Xu B,
Li W.-T,
Li M.-L,
Zhu S.-F,
*,
Houk KN,
*,
Zhou Q.-L.
*
Nankai University, Tianjin, P. R. of China and University of California, Los Angeles,
USA
Enantioselective Diarylcarbene Insertion into Si–H Bonds Induced by Electronic Properties
of the Carbenes.
J. Am. Chem. Soc. 2020;
142: 12394-12399
Key words
asymmetric catalysis - carbenes - rhodium catalysis - silanes
Significance
The authors describe a rhodium-catalyzed asymmetric coupling of silanes with diaryldiazomethanes.
The enantioselection is shown to be induced by the electronic properties of the aryl
substituents of the carbene rather than sterics.
Comment
DFT studies support the conclusion that, in the favored transition state, the more
electron-rich aryl group is coplanar with the carbene empty p-orbital while the other
ring is orthogonal, resulting in their differentiation.
