نتایج جستجو برای: aryl group

تعداد نتایج: 992563  

Journal: :Organic letters 2009
Da-Gang Yu Miao Yu Bing-Tao Guan Bi-Jie Li Yang Zheng Zhen-Hua Wu Zhang-Jie Shi

The Suzuki-Miyaura coupling of aryl nitriles with aryl/alkenyl boronic esters is reported. With this method, the cyano group could be applied as a protecting group of arenes and finally as a leaving group to further construct polyaryl scaffolds.

Journal: :Chemical communications 2013
Daniel J Tetlow Mark A Vincent Ian H Hillier Jonathan Clayden

Deprotonation with strong bases of N-vinyl ureas carrying an N'-aryl substituent leads to migration of the N'-aryl group from N to C via an allyllithium; with weaker bases and electron-deficient aryl rings the direction of the migration reverses, and aryl substituents α to the urea N atom may migrate from C to N.

Journal: :Journal of the American Chemical Society 2005
Pinjing Zhao John F Hartwig

beta-Aryl eliminations from a series of iminyl complexes to form rhodium aryl complexes and free nitriles are reported. Iminyl complexes [Rh(PEt3)3(N=CArAr')] were prepared from [Rh(COE)Cl]2, PEt3, LiN(SiMe3)2, and the imines HN=CArAr'. One example of these complexes was characterized by X-ray diffraction. Heating of these complexes in cyclohexane generated the rhodium aryl complexes and free n...

زرگری, مهریار , علیزاده, احد, موسوی, حدیث , گوهری, قربان , عابدینی, محمود , مهروز, عبدالکریم, هاشمی, سیدمحمدباقر ,

Background and purpose: Based on the epidemiologic studies, stroke has become one of the fundamental problems in the Middle East. Considering to the role of serum paraoxonase (PON1) in stroke, the present study designed to evaluate the prognostic importance of paraoxonase to arylesterase activity ratio (Para/Aryl) and ratios of the activities to HDL in nondiabetic patients with ischemic stroke....

Journal: :The Journal of organic chemistry 2011
Ming-Chang P Yeh Ming-Nan Lin Yi-Shiang Chou Tern-Chi Lin Li-Yu Tseng

The gold(I)-catalyzed hydroarylation of cyclohexa-1,3-dienes bearing an aryl group and a gem-diester in the tether proceeds in a 1,4-addition manner and in a diastereoselective fashion to afford perhydrophenanthrene rings. The reaction proceeded via attack of the aryl group onto the gold-activated cyclic dienes followed by rearomatization and protodeauration to generate perhydrophenanthrenes in...

Journal: :Synthesis 2021

Abstract N-Aryl-1,2,3,4-tetrahydroisoquinolines are obtained via a convenient and short protocol with broad range of substituents on both aromatic rings high functional group tolerance. Starting from readily available ortho-brominated aldehydes primary amines, condensation these building blocks under reductive conditions gives N-aryl 2-bromobenzylamines. The C-3/C-4-unit the tetrahydroisoquinol...

Journal: :World journal of emergency medicine 2014
Suat Zengin Behcet A Sahin Karta Basri Can Mustafa Orkmez Abdullah Taskin Ugur Lok Bediha Gulen Cuma Yildirim Seyithan Taysi

BACKGROUND Carbon monoxide poisoning (COP) is an important cause of mortality and morbidity worldwide. This study was to investigate the levels of serum paraoxonase (PON), arylesterase (ARYL), ceruloplasmin (Cp), and sulfhydryl (-SH) in the treatment of COP, and to further understand the pathophysiology of COP. METHODS This prospective study comprised 107 individuals with COP (group 1) and 50...

2016
Jakub Saadi Christoph Bentz Kai Redies Dieter Lentz Reinhold Zimmer Hans-Ulrich Reissig

Starting from γ-ketoesters with an o-iodobenzyl group we studied a palladium-catalyzed cyclization process that stereoselectively led to bi- and tricyclic compounds in moderate to excellent yields. Four X-ray crystal structure analyses unequivocally defined the structure of crucial cyclization products. The relative configuration of the precursor compounds is essentially transferred to that of ...

2015
Xing-Wang Lan Nai-Xing Wang Cui-Bing Bai Wei Zhang Yalan Xing Jia-Long Wen Yan-Jing Wang Yi-He Li

A novel and convenient copper (II) bromide and 1,8-diazabicyclo[5.4.1]undec-7-ene (DBU) or 1,10-phenanthroline catalysis protocol for the construction of α-alkyl-β-keto sulfones via C(sp(3))-H bond functionalization followed by C(sp(3))-S bond formation between aryl ketones and sodium sulfinates at room temperature has been developed. This method is applicable to a wide range of aryl ketones an...

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