Oxidative [4+2] annulation of styrenes with alkynes under external-oxidant-free conditions
A sequence of a Diels–Alder reaction and oxidation is a powerful route to valuable aromatic compounds. Here, the authors report a more atom-economical oxidant-free strategy involving a Diels–Alder with H2 evolution under noble-metal-free photoredox conditions.
Main Authors: | Guoting Zhang, Yulin Lin, Xu Luo, Xia Hu, Cong Chen, Aiwen Lei |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2018-03-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-03534-z |
Similar Items
-
External oxidant-free electrooxidative [3 + 2] annulation between phenol and indole derivatives
by: Kun Liu, et al.
Published: (2017-10-01) -
Rhodium-Catalyzed Oxidative Annulation of 2- or 7-Arylindoles with Alkenes/Alkynes Using Molecular Oxygen as the Sole Oxidant Enabled by Quaternary Ammonium Salt
by: Weihui Zhuang, et al.
Published: (2021-09-01) -
Cobalt-Catalyzed Annulation of Salicylaldehydes and Alkynes to Form Chromones and 4-Chromanones
by: Yang, Junfeng, et al.
Published: (2017) -
Visible light mediated intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes
by: Theresa H. Nguyen, et al.
Published: (2014-04-01) -
Synthesis of indoles via palladium-catalyzed annulation of aryl chlorides and internal alkynes
by: Dussault, Daemian David, 1973-
Published: (2006)