Cu-Catalyzed selective cascade sp(3) C-H bond oxidative functionalization towards isoxazoline derivatives.

Chem Commun (Camb)

State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China.

Published: April 2015

The first Cu-catalyzed cascade sp(3) C-H bond oxidative functionalization of the 2-ethylazaarenes has been developed. The two different sp(3) C-H bonds in 2-ethylazaarenes are selectively oxidized and four new types of bonds (C=O, C=N, C-C, C-O) are constructed in one operation. Starting from the simple substrates and cheap nitro source, this reaction provides an efficient approach to produce new kinds of isoxazolines.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c5cc01004gDOI Listing

Publication Analysis

Top Keywords

sp3 c-h
12
cascade sp3
8
c-h bond
8
bond oxidative
8
oxidative functionalization
8
cu-catalyzed selective
4
selective cascade
4
functionalization isoxazoline
4
isoxazoline derivatives
4
derivatives cu-catalyzed
4

Similar Publications

Palladium(II)-catalyzed C-H functionalization has attracted considerable attention as a pathway to late-stage modification of peptides. Herein, we report the Pd-catalyzed C(sp3)-H arylation of peptides directed by an amidoxime ether, which can be easily incorporated into peptides at any amide bond. Site- and stereoselective arylation of peptides has been achieved, including an unprecedented example of C-H arylation of an internal residue.

View Article and Find Full Text PDF

This study evaluates the deposition of diamond-like carbon (DLC) films with copper impurities on a glass substrate using simultaneous direct current (DC) and radio frequency (RF) magnetron sputtering. The structural, optical, electrical, and mechanical properties, as well as the surface topography of the films, were investigated under various DC power levels using Raman spectroscopy, ellipsometry, UV-VIS, I-V measurements, nanoindentation, AFM, and FESEM. Results indicate that increasing the DC power to the graphite target from 60 to 120 , while maintaining a constant 10  of RF power to the copper target, enhances the optical absorption coefficient of the films and increases the optical bandgap from 0.

View Article and Find Full Text PDF

C-C bond coupling with sp C-H bond via active intermediates from CO hydrogenation.

Nat Commun

January 2025

Key Laboratory of advanced catalysis, College of Chemistry and Chemical Engineering, Lanzhou University, 730000, Lanzhou, China.

Article Synopsis
  • CO hydrogenation has been identified as a more sustainable and efficient alternative to methanol in the side-chain alkylation of 4-methylpyridine (MEPY) using a ZnZrO/CsX tandem catalyst, achieving a conversion rate of 19.6%.
  • This new method results in 82% selectivity for 4-ethylpyridine (ETPY) and demonstrates 6.5 times greater activity compared to traditional methanol-mediated processes.
  • The success of this catalytic process is attributed to the dual functionality of the catalyst components, facilitating both CO hydrogenation and the activation of C-H and C-C bonds, with CHO* species acting as the crucial intermediate.
View Article and Find Full Text PDF

C(sp3)-H Bond Functionalization of 8-Methylquinolines.

Chem Asian J

December 2024

CSIR-IHBT: Institute of Himalayan Bioresource Technology CSIR, Chemical Technology, Palampur, India, Palampur, 176061, Palampur, INDIA.

Quinolines have emerged as essential components in various medicinal agents, playing a key role in treating various ailments. Numerous drugs with a quinoline core have been recognized for their antimalarial, antibacterial, and anticancer activities and have been successfully commercialized, including chloroquine, ciprofloxacin, topotecan, etc. Over the past two decades, we have witnessed a tremendous expansion in the C-H bond functionalization of quinoline scaffolds to widen this chemical space for drug discovery further.

View Article and Find Full Text PDF

Biocatalytic C-H oxidation meets radical cross-coupling: Simplifying complex piperidine synthesis.

Science

December 2024

Department of Chemistry, Scripps Research, 10550 North Torrey Pines Road, La Jolla, CA, USA.

Modern medicinal chemists are targeting more complex molecules to address challenging biological targets, which leads to synthesizing structures with higher sp character (Fsp) to enhance specificity as well as physiochemical properties. Although traditional flat, high-fraction sp molecules, such as pyridine, can be decorated through electrophilic aromatic substitution and palladium (Pd)-based cross-couplings, general strategies to derivatize three-dimensional (3D) saturated molecules are far less developed. In this work, we present an approach for the rapid, modular, enantiospecific, and diastereoselective functionalization of piperidine (saturated analog of pyridine), combining robust biocatalytic carbon-hydrogen oxidation with radical cross-coupling.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!