Carbene-catalyzed α-carbon amination of chloroaldehydes for enantioselective access to dihydroquinoxaline derivatives
An NHC-catalyzed α-carbon amination of chloroaldehydes was developed. Cyclohexadiene-1,2-diimines are used as amination reagents and four-atom synthons. Our reaction affords optically enriched dihydroquinoxalines that are core structures in natural products and synthetic bioactive molecules.
Saved in:
Main Authors: | Huang, Ruoyan, Chen, Xingkuan, Mou, Chengli, Luo, Guoyong, Li, Yongjia, Li, Xiangyang, Xue, Wei, Jin, Zhichao, Chi, Robin Yonggui |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2020
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/137763 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Carbene-catalyzed [4 + 2] cycloadditions of vinyl enolate and (in situ generated) imines for enantioselective synthesis of quaternary α-amino phosphonates
by: Sun, Jun, et al.
Published: (2020) -
Carbene-catalyzed access to thiochromene derivatives: control of reaction pathways via slow release of thiols from disulfides
by: Wu, Qifei, et al.
Published: (2023) -
N-Heterocyclic carbene organocatalysis : activation modes and typical reactive intermediates
by: Chen, Xingkuan, et al.
Published: (2022) -
Carbene-catalyzed direct functionalization of the β-sp3 -carbon atoms of α-chloroaldehydes
by: Liu, Bin, et al.
Published: (2020) -
Carbene-catalyzed enantioselective addition of thioamides to bromoenals for access to thiazinone heterocycles
by: Liu, Changyi, et al.
Published: (2020)