Desulfonylation via radical process: recent developments in organic synthesis

XQ Chu, D Ge, YY Cui, ZL Shen, CJ Li - Chemical reviews, 2021 - ACS Publications
As the “chemical chameleon”, sulfonyl-containing compounds and their variants have been
merged with various types of reactions for the efficient construction of diverse molecular …

Stereoelectronic power of oxygen in control of chemical reactivity: the anomeric effect is not alone

IV Alabugin, L Kuhn, MG Medvedev… - Chemical Society …, 2021 - pubs.rsc.org
Although carbon is the central element of organic chemistry, oxygen is the central element of
stereoelectronic control in organic chemistry. Generally, a molecule with a C–O bond has …

Amine-catalyzed synthesis of N2-sulfonyl 1, 2, 3-triazole in water and the tunable N2-H 1, 2, 3-triazole synthesis in DMSO via metal-free enamine annulation

Y Guo, Y Liu, JP Wan - Chinese Chemical Letters, 2022 - Elsevier
The selective synthesis of N 2-sulfonyl and N 2-H 1, 2, 3-triazoles via organocatalytic
annulation of enaminone/enaminoester with sulfonyl azide has been realized. The …

[HTML][HTML] A recent overview on the synthesis of 1, 4, 5-trisubstituted 1, 2, 3-triazoles

P Shiri, AM Amani, T Mayer-Gall - Beilstein Journal of Organic …, 2021 - beilstein-journals.org
Diverse strategies for the efficient and attractive synthesis of a wide variety of relevant 1, 4, 5-
trisubstituted 1, 2, 3-triazole molecules are reported. The synthesis of this category of diverse …

A one-pot photocatalytic triazole-based linkerology for PROTACs

J Liu, Y Deng, J Yin, J Ji, C Guan, X Chen, X Wu… - Cell Reports Physical …, 2024 - cell.com
Proteolysis-targeting chimeras (PROTACs) are a powerful approach for targeted protein
degradation. One of the current bottlenecks for developing PROTACs is the lack of an …

Iodide ion-enabled highly regioselective α-C (sp 3)–H triazolization of ethers with N-sulfonyl-1, 2, 3-triazoles

Y Deng, J Yin, Z Hu, J Xue, J Ji, T Zhu… - New Journal of Chemistry, 2024 - pubs.rsc.org
An efficient iodide ion (I−)-enabled method for direct α-C (sp3)–H triazolization of ethers via
a radical cross-coupling has been developed for regioselective construction of N2 …

Regioselectively Electrochemical Synthesis of N2-Selective C–H Amination of Ethers with N-Tosyl 1,2,3-Triazole via Triazole Radical Cation

C Guan, J Yin, J Ji, J Liu, X Wu, T Zhu, S Liu - Organic Letters, 2023 - ACS Publications
A regioselective electrochemical C–H amination method to synthesize N 2-substituted 1, 2, 3-
triazole using easily accessible ethers has been developed. Various substituents, including …

C (sp2)–H Bond Multiple Functionalization in Air for Construction of Tetrahydrocarbazoles with Continuous Quaternary Carbons and Polycyclic Diversification

L Song, D Ni, S Jia, R Pi, S Dong, F Yang, J Tang… - Organic …, 2020 - ACS Publications
The C (sp2)–H function of indole ketone with diazo compound via a rhodium (II)-catalyzed
intramolecular electrophilic trapping reaction under mild conditions in air was demonstrated …

Recent progress on synthesis of functionalized 1, 5-disubstituted triazoles

MK Jaiswal, A Gupta, FJ Ansari… - Current Organic …, 2024 - ingentaconnect.com
Immediately after the invention of 'Click Chemistry'in 2002, the regioselective 1, 2, 3-triazole
scaffolds resulted from respective organic azides and terminal alkynes under Cu (I) catalysis …

Discovery of potent thiazolidin-4-one sulfone derivatives for inhibition of proliferation of osteosarcoma in vitro and in vivo

X Chen, Z Luo, Z Hu, D Sun, Y He, J Lu, L Chen… - European Journal of …, 2024 - Elsevier
Chemotherapy combining with surgical treatment has been the main strategy for
osteosarcoma treatment in clinical. Due to unclear pathogenesis and unidentified drug …