The expanding role of pyridine and dihydropyridine scaffolds in drug design
Y Ling, ZY Hao, D Liang, CL Zhang… - Drug design …, 2021 - Taylor & Francis
Pyridine-based ring systems are one of the most extensively used heterocycles in the field of
drug design, primarily due to their profound effect on pharmacological activity, which has led …
drug design, primarily due to their profound effect on pharmacological activity, which has led …
Advances in catalytic asymmetric dearomatization
C Zheng, SL You - ACS Central Science, 2021 - ACS Publications
Asymmetric catalysis has been recognized as the most enabling strategy for accessing
chiral molecules in enantioenriched forms. Catalytic asymmetric dearomatization is an …
chiral molecules in enantioenriched forms. Catalytic asymmetric dearomatization is an …
A perspective on late-stage aromatic C–H bond functionalization
L Zhang, T Ritter - Journal of the American Chemical Society, 2022 - ACS Publications
Late-stage functionalization of C–H bonds (C–H LSF) can provide a straightforward
approach to the efficient synthesis of functionalized complex molecules. However, C–H LSF …
approach to the efficient synthesis of functionalized complex molecules. However, C–H LSF …
Recent Advances in Oxidative R1-H/R2-H Cross-Coupling with Hydrogen Evolution via Photo-/Electrochemistry: Focus Review
H Wang, X Gao, Z Lv, T Abdelilah, A Lei - Chemical reviews, 2019 - ACS Publications
Photo-/electrochemical catalyzed oxidative R1-H/R2-H cross-coupling with hydrogen
evolution has become an increasingly important issue for molecular synthesis. The dream of …
evolution has become an increasingly important issue for molecular synthesis. The dream of …
[HTML][HTML] Installing the “magic methyl”–C–H methylation in synthesis
D Aynetdinova, MC Callens, HB Hicks… - Chemical Society …, 2021 - pubs.rsc.org
The selective and efficient C–H methylation of sp2 and sp3 carbon centres has become a
powerful transformation in the synthetic toolbox. Due to the potential for profound changes to …
powerful transformation in the synthetic toolbox. Due to the potential for profound changes to …
The hitchhiker's guide to flow chemistry∥
Flow chemistry involves the use of channels or tubing to conduct a reaction in a continuous
stream rather than in a flask. Flow equipment provides chemists with unique control over …
stream rather than in a flask. Flow equipment provides chemists with unique control over …
Synthesis of vinylene-linked covalent organic frameworks by monomer self-catalyzed activation of knoevenagel condensation
Reticular chemistry based on thermodynamically controlled linking modes and numerous
organic building blocks has constituted versatile crystalline frameworks in molecular-level …
organic building blocks has constituted versatile crystalline frameworks in molecular-level …
Radical and ionic meta-C–H functionalization of pyridines, quinolines, and isoquinolines
Carbon-hydrogen (C− H) functionalization of pyridines is a powerful tool for the rapid
construction and derivatization of many agrochemicals, pharmaceuticals, and materials …
construction and derivatization of many agrochemicals, pharmaceuticals, and materials …
Metal-Free Amino (hetero) arylation and Aminosulfonylation of Alkenes Enabled by Photoinduced Energy Transfer
XK Qi, MJ Zheng, C Yang, Y Zhao… - Journal of the American …, 2023 - ACS Publications
β-(Hetero) arylethylamines are privileged structural motifs found in many high-value organic
molecules, including pharmaceuticals and natural products. To construct these important …
molecules, including pharmaceuticals and natural products. To construct these important …
Triazines: Syntheses and inverse electron-demand diels–alder reactions
FG Zhang, Z Chen, X Tang, JA Ma - Chemical Reviews, 2021 - ACS Publications
Triazines are an important class of six-membered aromatic heterocycles possessing three
nitrogen atoms, resulting in three types of regio-isomers: 1, 2, 4-triazines (a-triazines), 1, 2, 3 …
nitrogen atoms, resulting in three types of regio-isomers: 1, 2, 4-triazines (a-triazines), 1, 2, 3 …