Abstract
The regioselective addition of hydrazones and related N-nucleophiles to substituted terpene-based substrates can be steered to either 1,2- or 1,4-addition products, making this a potentially powerful protocol for the preparation of amines from biorelevant feedstocks via C-N bond formation. © 2013 The Royal Society of Chemistry.
Cite
CITATION STYLE
APA
Perrier, A., Ferreira, M., Reek, J. N. H., & Van Der Vlugt, J. I. (2013). Regioselective Pd-catalyzed hydroamination of substituted dienes. Catalysis Science and Technology, 3(5), 1375–1379. https://doi.org/10.1039/c3cy00024a
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