Visible light-induced organophotoredox-catalyzed difunctionalization of alkenes and alkynes
In the era of organic synthesis, the direct difunctionalization strategies of alkenes and
alkynes are very eminent, which open up an excellent route to introduce two functional …
alkynes are very eminent, which open up an excellent route to introduce two functional …
Electrochemical functionalization of imidazopyridine and indazole: An overview
Electrochemical synthesis offers a mild, simple, and efficient tool for the preparation of
interesting and useful molecules, thus eluding severe chemical oxidizing and reducing …
interesting and useful molecules, thus eluding severe chemical oxidizing and reducing …
Electrochemical Radical–Radical Cross-Coupling Approach between Sodium Sulfinates and 2H-Indazoles to 3-Sulfonylated 2H-Indazoles
W Kim, HY Kim, K Oh - Organic Letters, 2020 - ACS Publications
A direct cross-coupling between sodium sulfinates and 2 H-indazoles has been developed
under electrochemical conditions. The utilization of a graphite anode and platinum cathode …
under electrochemical conditions. The utilization of a graphite anode and platinum cathode …
Recent progress in sulfonylation via radical reaction with sodium sulfinates, sulfinic acids, sulfonyl chlorides or sulfonyl hydrazides
DQ Dong, QQ Han, SH Yang, JC Song, N Li… - …, 2020 - Wiley Online Library
Sodium sulfinates, sulfinic acids, sulfonyl chlorides and sulfonyl hydrazides as readily
available and efficient sulfonylation reagents have been extensively explored in recent …
available and efficient sulfonylation reagents have been extensively explored in recent …
Visible light-induced functionalization of indazole and pyrazole: a recent update
Indazole and pyrazole are renowned as a prodigious class of heterocycles having versatile
uses in medicinal as well as industrial chemistry. Considering sustainable approaches …
uses in medicinal as well as industrial chemistry. Considering sustainable approaches …
An update on the use of sulfinate derivatives as versatile coupling partners in organic chemistry
J Aziz, A Hamze - Organic & Biomolecular Chemistry, 2020 - pubs.rsc.org
The use of sulfinic acids and their salts continues to be extensively developed in organic
chemistry. This is attributable to their dual capacity for acting as nucleophilic or electrophilic …
chemistry. This is attributable to their dual capacity for acting as nucleophilic or electrophilic …
Recent advances in the application of sulfinic acids for the construction of sulfur-containing compounds
Y Lv, H Cui, N Meng, H Yue, W Wei - Chinese Chemical Letters, 2022 - Elsevier
Sulfur-containing organic compounds display wide applications in the field of materials
science, synthetic chemistry, and pharmaceutical industry. Thus, numerous synthetic …
science, synthetic chemistry, and pharmaceutical industry. Thus, numerous synthetic …
N‐Heteroarylation of Sulfonamides: An Overview
N‐Heteroaryl sulfonamides are an extremely significant variety of organosulfur compounds
that are present in many significant FDA‐approved drugs and therapeutic agents. Therefore …
that are present in many significant FDA‐approved drugs and therapeutic agents. Therefore …
Advances in oxosulfonylation reaction
Oxosulfonylation is a difunctionalization protocol where oxo and sulfonyl groups are
introduced in one step to construct ketosulfones and N‐acylsulfonamides from simple and …
introduced in one step to construct ketosulfones and N‐acylsulfonamides from simple and …
Electrochemically promoted C-3 amination of 2 H-indazoles
M Sun, Y Zhou, L Li, L Wang, Y Ma, P Li - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
This paper reports a metal-free and external oxidant-free electrochemical method for the C-3
amination of 2H-indazoles. The protocol employs commercially available azoles and …
amination of 2H-indazoles. The protocol employs commercially available azoles and …