Results 61 to 70 of about 81,920,088 (158)

Synthesis of Sulfur Heterocycles by Palladium‐Catalyzed Cyclization

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 14, 15 April 2026.
In spite of the well‐known palladium thiophilicity, sulfur‐containing acyclic substrates may efficiently undergo several different kinds of palladium‐catalyzed cyclization processes leading to highly important sulfur heterocycles in one synthetic step. Advances in this challenging and stimulating field of research are presented in this review.
Bartolo Gabriele
wiley   +1 more source

Rhodium-Catalyzed Highly Regioselective C-H Arylation of Imidazo[1,2-a]pyridines with Aryl Halides and Triflates [PDF]

open access: yes, 2013
A convenient Rh-catalyzed C-H arylation of imidazo[1,2-a]pyridines with a variety of aryl halides or triflates has been reported. This process afforded a range of biaryl compounds in excellent yields and showed high activity and broad scope.
Guoqiang Yin   +4 more
core  

Access to sulfonylated furans or imidazo[1,2-a]pyridines via a metal-free three-component, domino reaction [PDF]

open access: yes, 2018
An efficient three-component reaction for the synthesis of sulfonylated furans or imidazo[1,2-a]pyridines has been developed.
Xuechen Li   +3 more
core   +1 more source

Substitutive Approach Toward Heteroaromatic Amino Alcohols Accessed Through Dioxolanyl Radical Linchpin

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 7, 1 April 2026.
A dioxolanyl linchpin has been used to synthesize aryl ethanolamines from readily available aryl bromide and amine starting materials using a metallaphotoredox/substitution telescoped sequence. This combinatorial approach allows for a wide synthetic scope of both heteroarenes and cyclic amines. Aryl ethanolamines are an important functional group found
Justin J. Chang   +4 more
wiley   +1 more source

Solid-Phase Synthesis of Imidazo[1,2-a]pyridine Using Sodium Benzenesulfinate as a Traceless Linker [PDF]

open access: yes, 2016
The preparation of the first library of imidazo[1,2-a]pyridine derivatives on a solid support is described. A sulfone linker strategy was applied in the synthesis.
Yulin Lam (428621)   +2 more
core   +3 more sources

N,N-dimethylacetamide (DMA) as a methylene synthon for regioselective linkage of imidazo[1,2-a]pyridine [PDF]

open access: yes, 2016
A copper(II)‐catalyzed oxidative methylene‐bridged dimerization of two analogous imidazo[1,2‐a]pyridines has been achieved using N,N‐dimethylacetamide (DMA) as solvent cum methylene source.
Modi, Anju, Ali, Wajid, Patel, Bhisma K.
core   +1 more source

Two‐Step Access to 4‐Aryl‐5‐Heteroarylpyrazoles via Palladium‐Catalyzed Sequential Transformations Using Palladium 1,4‐Migration Tool

open access: yesAsian Journal of Organic Chemistry, Volume 15, Issue 4, April 2026.
Access to pyrazoles arylated at C4 and C5 positions remains challenging due to their similar reactivity under Pd‐catalyzed C–H activation conditions. Herein, we report on the synthesis of 4‐aryl‐5‐heteroarylpyrazoles involving Suzuki‐coupling, followed by Pd‐catalyzed C–H heteroarylation.
Bo Lan, Thierry Roisnel, Henri Doucet
wiley   +1 more source

Correction: Cu(i)-catalyzed double C–H amination: synthesis of 2-iodo-imidazo[1,2-a]pyridines [PDF]

open access: yes, 2017
Correction for ‘Cu(i)-catalyzed double C–H amination: synthesis of 2-iodo-imidazo[1,2-a]pyridines’ by Divya Dheer et al., RSC Adv., 2016, 6, 38033–38036.
Parthasarathi Das   +5 more
core   +1 more source

Covalent conjugates of isoflavone formononetine and its synthetitc analogues with imidazo[1,2-a]pyridines, imidazo[1,2-a]pyrimidines and imidazo[1,2-a]thiazoles [PDF]

open access: yes, 2008
Шляхом взаємодії 2-бромометильних похідних імідазо[1,2-a]піридину, імідазо[1,2-a]піримідину й імідазо[2,1-b]тіазолу з природним 7-гідроксиізофлавоном формононетином і з двома його синтетичними аналогами синтезовано відповідні 7-(імідазо[1,2-a]гетарил-2 ...
Коваленко, Н.В.   +1 more
core   +2 more sources

Cu(OTf)2-catalyzed synthesis of imidazo[1,2-a]pyridines from α-diazoketones and 2-aminopyridines [PDF]

open access: yes, 2007
α-Diazoketones undergo smooth coupling with 2-aminopyridines in the presence of 10 mol % of copper(II) triflate to produce the corresponding 2-substituted imidazo[1,2-a]pyridines (IPs) in excellent yields with high selectivity.
Narsaiah, A. V.   +4 more
core   +1 more source

Home - About - Disclaimer - Privacy