Rhodium(III)‐Catalyzed Regioselective C−H Annulation and Alkenylation of 2‐Pyridones with Terminal Alkynes DOI
Jiajie Li, Xin Xu,

Zhenli Luo

et al.

Advanced Synthesis & Catalysis, Journal Year: 2022, Volume and Issue: 364(7), P. 1264 - 1270

Published: Feb. 19, 2022

Abstract Cp*Rh(III)‐catalyzed regioselective C−H annulation and alkenylation of 2‐pyridones with terminal alkynes have been developed. The cationic Cp*Rh(III) catalytic system containing FeCl 3 additive enables 1‐(2‐pyridyl)‐2‐pyridones alkynes, providing efficient access to 5,7‐diarylated 2‐quinolinones. reaction pathway can be switched [Cp*RhCl 2 ] as the catalyst, NaOAc HOAc solvent, affording C6‐alkenylated in high yields. These protocols accommodate a wide range substrates good functional group compatibility. magnified image

Language: Английский

Application of sulfoxonium ylide in transition-metal-catalyzed C-H bond activation and functionalization reactions DOI
Anil Kumar, Mahadev Sharanappa Sherikar, Vinayak Hanchate

et al.

Tetrahedron, Journal Year: 2021, Volume and Issue: 101, P. 132478 - 132478

Published: Oct. 8, 2021

Language: Английский

Citations

70

Multiple annulations of inert C(sp2)–H bonds with alkynes DOI
Arijit Saha, Majji Shankar, Somratan Sau

et al.

Chemical Communications, Journal Year: 2022, Volume and Issue: 58(29), P. 4561 - 4587

Published: Jan. 1, 2022

This feature article uncovers a tactical blueprint for the sustainable development of synthetic manifestations in transition-metal catalyzed directing group assisted multiple annulations (L-type, Y-type, and B-type) inert C(arene)–H bonds.

Language: Английский

Citations

52

Deacylation-aided C–H alkylative annulation through C–C cleavage of unstrained ketones DOI
Xukai Zhou, Yan Xu, Guangbin Dong

et al.

Nature Catalysis, Journal Year: 2021, Volume and Issue: 4(8), P. 703 - 710

Published: Aug. 2, 2021

Language: Английский

Citations

52

Synthesis of CF3-Substituted N-Heterocyclic Compounds Based on C–H Activation-Initiated Formal [2 + 3] Annulation Featuring with a Latent Nucleophilic Site DOI

Manqing Wang,

Shengnan Yan,

Bin Li

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(11), P. 7828 - 7842

Published: May 22, 2024

Presented herein is a novel synthesis of CF

Language: Английский

Citations

6

Cationic π-extended heteroaromatics via a catalytic C–H activation annulative alkyne-insertion sequence DOI
Pirudhan Karak,

Samim Sohel Rana,

Joyanta Choudhury

et al.

Chemical Communications, Journal Year: 2021, Volume and Issue: 58(2), P. 133 - 154

Published: Nov. 10, 2021

Herein, the recent progress of an annulative alkyne-insertion π-extension (AAIPEX) strategy to construct opto-electronically significant cationic polycyclic heteroaromatic compounds (cPHACs) is showcased.

Language: Английский

Citations

34

Transition Metal‐Catalyzed C−H Functionalization Through Electrocatalysis DOI
Prabhat Kumar Baroliya, Mukesh Dhaker, Subir Panja

et al.

ChemSusChem, Journal Year: 2023, Volume and Issue: 16(12)

Published: March 7, 2023

Electrochemically promoted transition metal-catalyzed C-H functionalization has emerged as a promising area of research over the last few decades. However, development in this field is still at an early stage compared to traditional reactions using chemical-based oxidizing agents. Recent reports have shown increased attention on electrochemically functionalization. From standpoint sustainability, environmental friendliness, and cost effectiveness, oxidation metal catalyst offers mild, efficient, atom-economical alternative chemical oxidants. This Review discusses advances metal-electrocatalyzed past decade describes how unique features electricity enable economic sustainable way.

Language: Английский

Citations

13

Synthesis of CF3-Azafluorenes through the Cascade Reaction of 2H-Imidazoles with CF3-Ynones DOI
Hao Li,

Shengnan Yan,

Chunhua Ma

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 25, 2024

A concise synthesis of trifluoromethyl (CF

Language: Английский

Citations

5

Enantioselective Nickel‐Catalyzed C(sp3)−H Activation of Formamides DOI

Yin‐Xia Wang,

Feng‐Ping Zhang,

Hao Chen

et al.

Angewandte Chemie International Edition, Journal Year: 2022, Volume and Issue: 61(42)

Published: Aug. 29, 2022

Enantioselective Ni-catalyzed C(sp3 )-H bond activation remains an elusive challenge. Herein, we used phosphine oxide-ligated Ni-Al bimetallic catalyst to realize enantioselective aliphatic of formamides, providing a series chiral N-containing heterocycles in 40-95 % yield and 70-95 ee.

Language: Английский

Citations

19

Cascade C–H Activation/Annulation of Sulfoxonium Ylides with Vinyl Cyclopropanes: Access to Cyclopropane-Fused α-Tetralones DOI
Sharajit Saha, Bijoy Debnath, Kangkan Talukdar

et al.

Organic Letters, Journal Year: 2023, Volume and Issue: 25(19), P. 3352 - 3357

Published: May 4, 2023

Rh-catalyzed weak and traceless directing-group-assisted cascade C–H activation annulation of sulfoxonium ylides with vinyl cyclopropanes as a coupling partner have been accomplished to furnish functionalized cyclopropane-fused tetralones at moderate temperature. The C–C bond formation, cyclopropanation, functional group tolerance, late-stage diversifications drug molecules, scale-up are the important practical features.

Language: Английский

Citations

12

[4 + 2] Cyclization or Lossen Rearrangement: Rhodium-Catalyzed Divergent Synthesis of Carboline Derivatives with Anticancer Activity DOI

Lijie Lv,

Jia Zheng,

Yijie Xiao

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: 26(20), P. 4212 - 4217

Published: May 14, 2024

An unusual rhodium-catalyzed C–H activation/Lossen rearrangement/oxa-Michael addition tandem cyclization has been achieved along with a tunable well-known activation/[4 + 2] annulation, leading to regio-, chemo-, and diastereoselective access diverse pentacyclic α-carbolines β-carboline-1-one derivatives in moderate good yields significant anticancer activity.

Language: Английский

Citations

4