Asymmetric Three-Component Heck Arylation/Amination of Nonconjugated Cyclodienes

49Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Substituted cyclohexylamines are becoming increasingly important in drug discovery. Asymmetric Heck insertion/amination of nonconjugated cyclodienes proceeds to give 5-aryl cyclohexenylamines with good enantioselectivity and exclusive trans configurations. Primary and secondary anilines, indoline, and benzylamines are suitable amines. The weakly donating diphosphite Kelliphite forms a deep unsymmetrical pocket, which is essential for stereoselective anti attack of amines.

Cite

CITATION STYLE

APA

Zhu, D., Jiao, Z., Chi, Y. R., Gonçalves, T. P., Huang, K. W., & Zhou, J. S. (2020). Asymmetric Three-Component Heck Arylation/Amination of Nonconjugated Cyclodienes. Angewandte Chemie - International Edition, 59(13), 5341–5345. https://doi.org/10.1002/anie.201915864

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free