Radical aryl migration enables diversity-oriented synthesis of structurally diverse medium/macro- or bridged-rings
Medium-sized ring systems are common in natural products, however their synthesis is challenging, largely due to entropic factors. Here the authors report a radical-based method for the synthesis of medium to large functionalized, carbon or heterocyclic scaffolds.
Saved in:
Main Authors: | Lei Li, Zhong-Liang Li, Fu-Li Wang, Zhen Guo, Yong-Feng Cheng, Na Wang, Xiao-Wu Dong, Chao Fang, Jingjiang Liu, Chunhui Hou, Bin Tan, Xin-Yuan Liu |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2016
|
Subjects: | |
Online Access: | https://doaj.org/article/b698f683d92844d7b96b0fb27ba6934b |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Diversity-oriented synthesis of nanographenes enabled by dearomative annulative π-extension
by: Wataru Matsuoka, et al.
Published: (2021) -
Diversity-oriented functionalization of 2-pyridones and uracils
by: Yong Shang, et al.
Published: (2021) -
Spatial modulation of individual behaviors enables an ordered structure of diverse phenotypes during bacterial group migration
by: Yang Bai, et al.
Published: (2021) -
Aryl radical-mediated N-heterocyclic carbene catalysis
by: Yuki Matsuki, et al.
Published: (2021) -
The effect of different drinking water in culture medium on feces microbiota diversity
by: Kun Zhou, et al.
Published: (2021)