Five-membered ring systems: With more than 1 N atom DOI
Larry Yet

Progress in heterocyclic chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 211 - 257

Published: Jan. 1, 2024

Language: Английский

Reactivity of α-diazo sulfonium salts: rhodium-catalysed ring expansion of indenes to naphthalenes DOI Creative Commons

Sven Timmann,

Tun-Hui Wu,

Christopher Golz

et al.

Chemical Science, Journal Year: 2024, Volume and Issue: 15(16), P. 5938 - 5943

Published: Jan. 1, 2024

Cyclopropyl-substituted sulfonium salts are obtained by Rh-catalysed addition of α-diazo dibenzothiophenium to olefins. When indenes used as substrates, initially formed cyclopropyl rings open with concomitant elimination dibenzothiophene, enabling access 2-substituted naphthalenes.

Language: Английский

Citations

11

Alkoxy Diazomethylation of Alkenes by Photoredox-Catalyzed Oxidative Radical-Polar Crossover DOI Creative Commons
Qiyuan He, Quan Zhang, Alessa B. Rolka

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(18), P. 12294 - 12299

Published: April 25, 2024

Herein, we present the discovery and development of first photoredox-catalyzed alkoxy diazomethylation alkenes with hypervalent iodine reagents alcohols. This multicomponent process represents a new disconnection approach to diazo compounds is featured by broad scope, mild reaction conditions, excellent selectivity. Key was generation diazomethyl radicals, which engaged alcohols in an inter- intramolecular fashion oxidative radical–polar crossover leading unexplored β-alkoxydiazo compounds. The synthetic utility such demonstrated series transformations involving C–H, N–H, O–H insertions as well construction complex sp3-rich heterocycles.

Language: Английский

Citations

6

Nitrogen-Based Organofluorine Functional Molecules: Synthesis and Applications DOI
Shuai Liu, Jun Zhou, Lu Yu

et al.

Chemical Reviews, Journal Year: 2025, Volume and Issue: unknown

Published: April 22, 2025

Fluorine and nitrogen form a successful partnership in organic synthesis, medicinal chemistry, material sciences. Although fluorine-nitrogen chemistry has long rich history, this field received increasing interest made remarkable progress over the past two decades, driven by recent advancements transition metal organocatalysis photochemistry. This review, emphasizing contributions from 2015 to 2023, aims update state of art synthesis applications nitrogen-based organofluorine functional molecules chemistry. In dedicated sections, we first focus on fluorine-containing reagents organized according type groups attached nitrogen, including N-F, N-RF, N-SRF, N-ORF. review also covers nitrogen-linked building blocks, catalysts, pharmaceuticals, agrochemicals, underlining these components' broad applicability growing importance modern

Language: Английский

Citations

0

A visible light-induced photoredox-catalyzed assembly-point di/trifunctionalization of diazomethyl radicals DOI

Xue-Cen Xu,

Yuan Sang,

Min Yang

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(19), P. 5502 - 5510

Published: Jan. 1, 2024

A visible light-induced di/trifunctionalization of diazo compounds with electron-rich arenes or alkenes has been developed. This provides a new strategy for the synthesis α,α-diaryl- and α,α,α-triaryl-carbonyl compounds, 1,4-dienes indolizines.

Language: Английский

Citations

1

Recent Highlights in the Synthesis and Biological Significance of Pyrazole Derivatives DOI Creative Commons
Ziad Moussa, Mani Ramanathan,

Shaikha Mohammad Alharmoozi

et al.

Heliyon, Journal Year: 2024, Volume and Issue: 10(20), P. e38894 - e38894

Published: Oct. 1, 2024

Language: Английский

Citations

1

Catalytic photoactivation of a triarylamine electron donor-acceptor complex for difunctionalization of alkenes DOI Creative Commons

Hao-Yan Wu,

Xiaodong Tang,

Ran Guo

et al.

Cell Reports Physical Science, Journal Year: 2024, Volume and Issue: 5(8), P. 102135 - 102135

Published: Aug. 1, 2024

The photoactivation of electron donor-acceptor complexes is a useful tool for the generation radical species in synthetic chemistry. However, alkene difunctionalization via catalytic remains less developed. Herein, we report versatile an complex platform alkenes without need precious transition metal catalysts or synthetically elaborate organic dyes. By taking advantage visible light potential aggregates between triarylamines and S-fluoromethyldiaryl sulfonium salts, photoinduced single-electron transfer initiated to generate stable cation, which acts as endogenous oxidant convert addition intermediate into cationic species. Subsequent N-nucleophilic enables styrenes. This general photocatalyst-free protocol applied fluoroalkylative sulfonamidation, amidation, hydrazidation, azidation, anilination reactions under mild conditions.

Language: Английский

Citations

0

Five-membered ring systems: With more than 1 N atom DOI
Larry Yet

Progress in heterocyclic chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 211 - 257

Published: Jan. 1, 2024

Language: Английский

Citations

0