C–H bond functionalization by high-valent cobalt catalysis: current progress, challenges and future perspectives
L Lukasevics, A Cizikovs, L Grigorjeva - Chemical Communications, 2021 - pubs.rsc.org
Over the last decade, high-valent cobalt catalysis has earned a place in the spotlight as a
valuable tool for C–H activation and functionalization. Since the discovery of its unique …
valuable tool for C–H activation and functionalization. Since the discovery of its unique …
Recent Advances in Cobalt‐Catalyzed, Directing‐Group‐Assisted C− H Bond Amidation Reactions
S Sunny, R Karvembu - Advanced Synthesis & Catalysis, 2021 - Wiley Online Library
C− N bond formation reactions have garnered a lot of interest in recent years due to the
predominance of nitrogen‐containing compounds in most pharmacological medications …
predominance of nitrogen‐containing compounds in most pharmacological medications …
The recent advances in cobalt-catalyzed C (sp 3)–H functionalization reactions
Over the past decades, reactions involving C–H functionalization have become a hot theme
in organic transformations because they have a lot of potential for the streamlined synthesis …
in organic transformations because they have a lot of potential for the streamlined synthesis …
Research progress of sulfoxonium ylides in the construction of five/six-membered nitrogen-containing heterocycles
Z Jiantao, Z Cong, Z Zidong, Z Peng… - Chinese Journal of …, 2022 - sioc-journal.cn
Sulfoxonium ylides are witnessed as powerful reagents for various organic transformations
due to its high stability and diverse reactivity in organic synthesis. The research progress of …
due to its high stability and diverse reactivity in organic synthesis. The research progress of …
Cp* Co III-catalyzed formal [4+ 2] cycloaddition of 2-phenyl-1 H-imidazoles to afford imidazo [1, 2-c] quinazoline derivatives
D Wu, Z Liu, Y Chang, J Chen, H Qi, Y Dong… - Organic & Biomolecular …, 2022 - pubs.rsc.org
A synthetic protocol based on Cp* CoIII-catalyzed C–H amidation/annulation of 2-aryl-1H-
imidazoles with 1, 4, 2-dioxazol-5-ones was developed to give imidazo [1, 2-c] quinazoline …
imidazoles with 1, 4, 2-dioxazol-5-ones was developed to give imidazo [1, 2-c] quinazoline …
Thioether-directed Rh (iii)-catalyzed peri-selective acyloxylation of arenes
H **e, JL Song, CY Jiang, YX Huang… - Organic & …, 2022 - pubs.rsc.org
A thioether directed acyloxylation of arenes has been realized via Cp* Rh (III)-catalyzed C–
H activation and subsequent coupling with carboxylic acids. This new method showed high …
H activation and subsequent coupling with carboxylic acids. This new method showed high …
Benzoisoxazoles as Privileged Scaffolds in the Design and Synthesis of N‐containing Molecules: A Recent Update
X Chen, W Ma, T Kang, P Sun… - European Journal of …, 2024 - Wiley Online Library
Benzoisoxazoles, with a distinctive 10‐π‐electron system and significant polarity, readily
trigger N− O bond cleavage, enabling multifaceted applications in organic synthesis. Over …
trigger N− O bond cleavage, enabling multifaceted applications in organic synthesis. Over …
[PDF][PDF] 亚砜叶立德参与构建五/六元氮杂环的反应研究进展
张建涛, 张聪, 郑梓栋, 周鹏, 刘卫兵 - Chin. J. Org. Chem, 2022 - scholar.archive.org
摘要亚砜叶立德因其在有机合成中的高稳定性和多样的反应性, 被视为各种有机转化的**大试剂
. 系统综述了亚砜叶立德参与构建含氮杂环化合物的反应研究进展, 总结了亚砜叶立德作为重要 …
. 系统综述了亚砜叶立德参与构建含氮杂环化合物的反应研究进展, 总结了亚砜叶立德作为重要 …