نتایج جستجو برای: heterogeneous oligomerization of olefins

تعداد نتایج: 21174884  

2014
Julian C. Lo Yuki Yabe Phil S. Baran

A redox-economic method for the direct coupling of olefins that uses an inexpensive iron catalyst and a silane reducing agent is reported. Thus, unactivated olefins can be joined directly to electron-deficient olefins in both intra- and intermolecular settings to generate hindered bicyclic systems, vicinal quaternary centers, and even cyclopropanes in good yield. The reaction is not sensitive t...

Journal: :Organic & biomolecular chemistry 2015
Qixue Qin Daan Ren Shouyun Yu

A visible-light-promoted chloramination of olefins is reported. N-Chlorosulfonamides serve as both nitrogen and chlorine sources. These reactions provide a simple, efficient, regioselective, and atom-economical method for the preparation of vicinal haloamine derivatives under mild reaction conditions. A variety of olefins were tolerated, and chloramination products were obtained in good yields.

2014
Michael R. Harris Mikhail O. Konev Elizabeth R. Jarvo

Enantioenriched methylenecyclopentanes are synthesized by stereospecific, nickel-catalyzed Heck cyclizations of secondary benzylic ethers. The reaction proceeds in high yield and enantiospecificity for benzylic ethers of both π-extended and simple arenes. Ethers with pendant 1,2-disubstituted olefins form trisubstituted olefins with control of both absolute configuration and alkene geometry. Di...

Journal: :Molecules 2010
Yasushi Obora Yasutaka Ishii

The direct aerobic coupling reaction of arenes with olefins was successfully achieved by the use of Pd(OAc)2/molybdovanadophosphoric acid (HPMoV) as a key catalyst under 1 atm of dioxygen. This catalytic system could be extended to the coupling reaction of various substituted benzenes with olefins such as acrylates, aclrolein, and ethylene through the direct aromatic C-H bond activation.

Journal: :Chemical communications 2013
Liena Qin Hajime Hirao Jianrong Steve Zhou

A regioselective Heck reaction of aliphatic olefins and aryl bromides is realized at internal carbons of olefins. Methanol solvent promoted halide ionization from neutral arylpalladium halide complexes via hydrogen bonding, so as to create cationic aryl-Pd species for regioselective olefin insertion.

Journal: :Chemical communications 2011
Christine A Caputo Zhongliang Zhu Zachary D Brown James C Fettinger Philip P Power

The reactions of Ar'GaGaAr' (Ar' = C(6)H(3)-2,6-(C(6)H(3)-2,6-(i)Pr(2))(2)) with alkenes revealed the addition of two olefins per Ar'GaGaAr' under ambient conditions for ethylene, propene, 1-hexene and styrene but no reactions with more hindered or cyclic olefins.

Journal: :Chemical communications 2007
Kasi Nehru Soo Jeong Kim In Young Kim Mi Sook Seo Youngmee Kim Sung-Jin Kim Jinheung Kim Wonwoo Nam

A non-heme manganese(II) complex shows a high catalytic activity in the epoxidation of olefins by iodosyl benzene and in the oxidation of olefins, alcohols and alkanes by peracetic acid; a mechanism involving metal-based oxidants is proposed for the oxidation reactions.

Journal: :Molecules 2016
Alina Ciammaichella Valeria Cardoni Alessandro Leoni Pietro Tagliatesta

Cyclopropanation reaction is an important tool for obtaining interesting compounds and can be catalyzed by metalloporphyrins with high syn/anti ratio. The catalyst cannot be recycled and is usually lost during chromatographic separation from the two isomeric products. In this paper a meso-tetraphenylporphyrin rhodium(III) chloride was bound to a Merrifield resin and used to catalyze the cyclopr...

Ali Akbar Mirzaei, Mostafa Feyzi

A series of x(Co, Mn)/TiO2 catalysts (x=2–12wt.%) containing 25%Co and 75%Mn were prepared by the co-impregnation method. All prepared catalysts have been tested in Fischer-Tropsch synthesis for production of C2-C4 olefins. It was found that the catalyst containing 8wt.%(Co,Mn)/TiO2 is an optimal catalyst for production of C...

Journal: :Chemical communications 2013
Macharla Arun Kumar Peraka Swamy Mameda Naresh Marri Mahender Reddy Chozhiyath Nappunni Rohitha Sripadi Prabhakar Akella Venkata Subrahmanya Sarma Joseph Richard Prem Kumar Nama Narender

A new metal-free protocol is described for the synthesis of terminal acetals by tandem oxidative rearrangement of olefins using oxone as an oxidant in the presence of iodine. Moreover, a one-pot procedure for the preparation of glycol mono esters from olefins is also presented for the first time using the same reagent system.

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