Copper-catalyzed aerobic [3+2] : annulation of N-alkenyl amidines
A method for the synthesis of bi- and tricyclic amidines has been developed through copper-catalyzed aerobic [3+2]-annulation reaction of N-alkenyl amidines. These cyclic amidines could be converted into mono-benzyl-protected vicinal diamines by the reduction with aluminum hydride.
Saved in:
Main Authors: | Wang, Yi-Feng, Zhu, Xu, Chiba, Shunsuke |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2013
|
Online Access: | https://hdl.handle.net/10356/95814 http://hdl.handle.net/10220/11280 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Copper-catalyzed aerobic aliphatic C–H oxygenation directed by an amidine moiety
by: Wang, Yi-Feng, et al.
Published: (2013) -
Copper-catalyzed aerobic radical C-C bond cleavage of N-H ketimines
by: Tnay, Ya Lin, et al.
Published: (2016) -
Copper-catalyzed aerobic C-C bond cleavage of lactols with N-hydroxy phthalimide for synthesis of lactones
by: Tnay, Ya Lin, et al.
Published: (2015) -
Formal [4+2]-annulation of vinyl azides with N-unsaturated aldimines
by: Zhu, Xu, et al.
Published: (2014) -
Copper-catalyzed aerobic aliphatic C–H oxygenation with hydroperoxides
by: Too, Pei Chui, et al.
Published: (2014)