Synthesis of Sulfur Heterocycles by Palladium‐Catalyzed Cyclization
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]
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
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Access to sulfonylated furans or imidazo[1,2-a]pyridines via a metal-free three-component, domino reaction [PDF]
An efficient three-component reaction for the synthesis of sulfonylated furans or imidazo[1,2-a]pyridines has been developed.
Xuechen Li +3 more
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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]
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
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N,N-dimethylacetamide (DMA) as a methylene synthon for regioselective linkage of imidazo[1,2-a]pyridine [PDF]
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.
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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(
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
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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]
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
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Cu(OTf)2-catalyzed synthesis of imidazo[1,2-a]pyridines from α-diazoketones and 2-aminopyridines [PDF]
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
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