Exploration of visible-light photocatalysis in heterocycle synthesis and functionalization: reaction design and beyond
JR Chen, XQ Hu, LQ Lu, WJ **ao - Accounts of chemical research, 2016 - ACS Publications
Conspectus Visible-light photocatalysis has recently received increasing attention from
chemists because of its wide application in organic synthesis and its significance for …
chemists because of its wide application in organic synthesis and its significance for …
Benzannulation strategies for the synthesis of carbazoles, indolocarbazoles, benzocarbazoles, and carbolines
Nitrogen-containing π-excessive aromatic heterocycles, in particular, carbazoles,
indolocarbazoles, benzocarbazoles, and carbolines have been considered the fundamental …
indolocarbazoles, benzocarbazoles, and carbolines have been considered the fundamental …
Trends in carbazole synthesis–an update (2013–2023)
The interest of scientists in the carbazole core has risen steadily over the last 30 years,
particularly over the last decade given its presence in several active pharmaceutical …
particularly over the last decade given its presence in several active pharmaceutical …
Rh (III)-catalyzed [5+ 1] annulation of indole-enaminones with diazo compounds to form highly functionalized carbazoles
Z Jiang, J Zhou, H Zhu, H Liu, Y Zhou - Organic Letters, 2021 - ACS Publications
A novel Rh (III)-catalyzed C–H activation/annulation cascade of indole-enaminones with
diazo compounds was reported to construct diversely functionalized carbazole frameworks …
diazo compounds was reported to construct diversely functionalized carbazole frameworks …
Recent advances in the synthesis of carbazoles from indoles
T Aggarwal, AK Verma - Organic & Biomolecular Chemistry, 2019 - pubs.rsc.org
Carbazoles are privileged nitrogen heterocycles that are present in a wide range of natural
products, pharmaceuticals, and functional materials. Due to their wide application, various …
products, pharmaceuticals, and functional materials. Due to their wide application, various …
Recent Developments in Photo‐Catalyzed/Promoted Synthesis of Indoles and Their Functionalization: Reactions and Mechanisms
L Zheng, K Tao, W Guo - Advanced Synthesis & Catalysis, 2021 - Wiley Online Library
The use of clean and renewable light sources is increasingly common in organic synthesis
due to its safety, practicality and economy. Recently, photoredox catalysis has shown great …
due to its safety, practicality and economy. Recently, photoredox catalysis has shown great …
Visible light promoted difunctionalization reactions of alkynes
X Ren, Z Lu - Chinese Journal of Catalysis, 2019 - Elsevier
Visible light promoted difunctionalization of alkynes is reviewed. The difunctionalization
reaction is achieved by different reagents. Radicals such as carbon (sp 3), carbon (sp 2) …
reaction is achieved by different reagents. Radicals such as carbon (sp 3), carbon (sp 2) …
Visible-light photocatalytic bicyclization of β-alkynyl propenones for accessing diastereoenriched syn-fluoren-9-ones
ZJ Shen, HN Shi, WJ Hao, SJ Tu, B Jiang - Chemical Communications, 2018 - pubs.rsc.org
A novel visible-light photocatalytic bicyclization of β-alkynyl propenones with α-
bromocarbonyls for highly diastereoselective synthesis of richly decorated syn-fluoren-9 …
bromocarbonyls for highly diastereoselective synthesis of richly decorated syn-fluoren-9 …
Rhodium-catalyzed C2 and C4 C–H activation/annulation of 3-(1 H-indol-3-yl)-3-oxopropanenitriles with internal alkynes: a facile access to substituted and fused …
T Zhou, B Li, B Wang - Chemical Communications, 2017 - pubs.rsc.org
Rhodium-catalyzed oxidative annulation reactions of 3-(1H-indol-3-yl)-3-oxopropanenitriles
with internal alkynes have been developed. A series of substituted carbazoles and 4H …
with internal alkynes have been developed. A series of substituted carbazoles and 4H …
Photoredox Catalysis of Aromatic β‐Ketoesters for in Situ Production of Transient and Persistent Radicals for Organic Transformation
XL Yang, JD Guo, H **ao, K Feng… - Angewandte Chemie …, 2020 - Wiley Online Library
Radical formation is the initial step for conventional radical chemistry. Reported herein is a
unified strategy to generate radicals in situ from aromatic β‐ketoesters by using a …
unified strategy to generate radicals in situ from aromatic β‐ketoesters by using a …