Abstract
Reductions of chiral ketimines effected under H2 by catalytic amounts of B(C6F5)3 result in moderate to excellent diastereoselectivities. In the case of camphor and menthone derived imines, the reductions proceeded with greater than 95% diastereoselectivity. © 2011 The Royal Society of Chemistry.
Cite
CITATION STYLE
APA
Heiden, Z. M., & Stephan, D. W. (2011). Metal-free diastereoselective catalytic hydrogenations of imines using B(C6F5)3. Chemical Communications, 47(20), 5729–5731. https://doi.org/10.1039/c1cc10438a
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free