Handbook of CH‐Functionalization, Journal Year: 2022, Volume and Issue: unknown, P. 1 - 32
Published: Nov. 29, 2022
Abstract The uses of sulfur (S) atoms as the directing groups for CH bond functionalization are summarized.
Language: Английский
Handbook of CH‐Functionalization, Journal Year: 2022, Volume and Issue: unknown, P. 1 - 32
Published: Nov. 29, 2022
Abstract The uses of sulfur (S) atoms as the directing groups for CH bond functionalization are summarized.
Language: Английский
Chemical Society Reviews, Journal Year: 2022, Volume and Issue: 51(18), P. 7810 - 7882
Published: Jan. 1, 2022
Although C–H functionalization is one of the simplest reactions, it requires use highly active and selective catalysts. Recently, C–H-active transformations using porous materials such as crystalline metal-organic frameworks (MOFs) covalent-organic (COFs) well amorphous porous-organic polymers (POPs) new emerging heterogeneous catalysts have attracted significant attention due to their promising activity potential material tunability. These solids offer exceptional structural uniformity, facile tunability permanent porosity. In addition, tuning catalytic selectivity these can be achieved through engineering site microenvironments, metal node substitution, linker changes, node/linker functionalization, pore modification. The present review provides an overview current state art on MOFs, COFs POPs advanced for various bond activation providing details about chemo-, regio-, stereo-selectivity control, comparing performance with that other catalysts, triggering additional research by showing limitations challenges in this area, a perspective future developments.
Language: Английский
Citations
144Asian Journal of Organic Chemistry, Journal Year: 2019, Volume and Issue: 9(1), P. 116 - 120
Published: Dec. 21, 2019
Abstract A visible light‐ and heat‐promoted C‐O coupling reaction of phenols aryl halides has been described. Compared to the traditional reactions promoted by light, this strategy avoids use transition metals, photocatalysts ligands. Moreover, good substrate universality, suitable for substituted phenol, naphthol heterocyclic phenol derivatives.
Language: Английский
Citations
29The Journal of Organic Chemistry, Journal Year: 2020, Volume and Issue: 85(16), P. 11014 - 11024
Published: July 20, 2020
An efficient strategy for the construction of fused imidazole derivatives through a palladium-catalyzed isocyanide insertion reaction has been accomplished. The methodology provides an operationally simple and versatile route synthesis indeno[1,2-d]imidazole imidazo[1,2-a]indole skeletons which are rarely reported. key features protocol sequential C-C/C-C/C-N bonds via C(sp2)-H functionalization at C2- C4-position, respectively. compounds can be synthesized with diverse scaffolds, easily accessible starting materials, moderate to good yields.
Language: Английский
Citations
14ChemistrySelect, Journal Year: 2023, Volume and Issue: 8(5)
Published: Feb. 1, 2023
Abstract Herein, a straightforward method for the construction of tetrazole derivatives has been achieved through Pd‐catalyzed isocyanide insertion reactions, which is good extension response multi‐molecule isocyanides. The Ugi‐N 3 reaction was introduced to transformation enrich diversity skeleton structures. commercially available starting materials and moderate yields make this valuable tool generating N‐containing heterocyclic compounds.
Language: Английский
Citations
4ChemistrySelect, Journal Year: 2021, Volume and Issue: 6(45), P. 12921 - 12925
Published: Dec. 2, 2021
Abstract In this work, an efficient synthesis of indole derivatives through palladium‐catalyzed double isocyanide insertion reactions has been developed. The reaction intermediates could be readily obtained by Ugi reactions. transformation features broad functional‐group compatibility, commercially available starting materials, and moderate to good yields. Furthermore, the bioactivities synthesized compounds were evaluated in mycelial growth tests against Penicilium digitatum Colletotrichun gloeosporioides, showed potential antifungal activities.
Language: Английский
Citations
9Chinese Journal of Organic Chemistry, Journal Year: 2021, Volume and Issue: 41(6), P. 2374 - 2374
Published: Jan. 1, 2021
The tandem reaction strategy of Ugi four-component and its subsequent modification based on in situ capture amines to prepare three types six-and seven-membered nitrogen-heterocycles are reported.According this strategy, were synthesized immediately worked as the substrate for reaction.Starting from cheap easily available nitro compounds, application scope substrates has been expanded problems easy oxidation, poor stability versatility have solved.Furthermore, due atom economy versatility, become a new approach synthesis nitrogen-hete-rocycles.In addition, series conditional control experiments, plausible mechanism is proposed.Keywords amines; /Wittig reaction; reaction/Staudinger/aza-Wittig one-pot synthesis; heterocycles 多组分反应(MCR)因其具有较高的原子经济性、较 广泛的底物普适性、较高的产物选择性和一锅法所具备 的操作简便性等优点, 在新药研发以及新荧光材料的设 计 等 方 面 都 有 广 泛 的 应 用 [1] .近 年 来 , 发 展 较 快 Mannich 反应、Passerini 反应、Petasis 反应和 反应 等多组分反应被用于构建天然产物和各种杂环化合
Language: Английский
Citations
7Inorganica Chimica Acta, Journal Year: 2023, Volume and Issue: 554, P. 121546 - 121546
Published: May 2, 2023
Language: Английский
Citations
2Journal of the Iranian Chemical Society, Journal Year: 2020, Volume and Issue: 17(6), P. 1339 - 1345
Published: Jan. 28, 2020
Language: Английский
Citations
5Chinese Journal of Chemical Engineering, Journal Year: 2024, Volume and Issue: 70, P. 1 - 8
Published: March 23, 2024
Language: Английский
Citations
0Tetrahedron Letters, Journal Year: 2024, Volume and Issue: 140, P. 155046 - 155046
Published: April 1, 2024
Language: Английский
Citations
0