Dearomative dimerization of quinolines and their skeletal rearrangement to indoles triggered by single-electron transfer
Dearomatization of two-dimensional planar aromatic feedstocks is an attractive strategy for the introduction of three-dimensional vectors into chemical scaffolds to expand chemical space for drug discovery. Here, we demonstrate the dearomative dimerization and skeletal rearrangement of quinolines un...
Saved in:
Main Authors: | Tan, Eugene Yew Kun, Dehdari, Alireza, Lani, Amirah S. Mat, Pratt, Derek A., Chiba, Shunsuke |
---|---|
Other Authors: | School of Chemistry, Chemical Engineering and Biotechnology |
Format: | Article |
Language: | English |
Published: |
2025
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/182573 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Base-induced dehydrogenative and dearomative transformation of 1-naphthylmethylamines to 1,4-dihydronaphthalene-1-carbonitriles
by: Sekiguchi, Yoshiya, et al.
Published: (2023) -
Dearomatization of (hetero)arenes through photodriven interplay between polysulfide anions and formate
by: Tan, Eugene Yew Kun, et al.
Published: (2023) -
Indole alkaloids from the fruits of Alstonia scholaris
by: Lakhana Chaisri, 1972-
Published: (2007) -
Indole alkaloids from the stems of Uncaria homomalla
by: Kusuma Pasugdee, 1975-
Published: (2007) -
Physiological pharmacology of indole alkaloids from Uncaria salacensis
by: Uraipan Archongka
Published: (2012)