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11.
The cyclopalladated ferrocenylimine adducts Ia , Ib , Ic were evaluated in the Suzuki cross‐coupling reaction of benzyl halides with arylboronic acids. The tricyclohexylphosphine adduct Ia exhibited highly catalytic activity for the coupling of aryl and heteroaryl boronic acids containing various functional groups with benzylic bromides and chlorides (up to 99% yield), furnishing diarylmethane derivatives with low catalyst loading (1 mol%). It is worth noting that catalyst Ia can be reused eight times without losing its catalytic activity. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
12.
《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2343-2348
A simple method for the preparation of industrially important alkyl aryl ethers is reported. Several phenolic compounds such as phenols, naphthols, and hydroxy coumarins were O-methylated with trimethyl phosphite or trimethyl phosphate under microwave irradiation and solvent-free condition in almost quantitative yields. Reaction of 2-naphthol with trimethyl phosphate gave mixture of 2-methoxynaphthalene and 1-methyl-2-methoxynaphthalene while the reaction with trimethyl phosphite gave mostly 2-methoxynaphthalene. This method is highly efficient for the methylating of phenolic compounds with very easy experimental procedure and environmental friendly conditions. 相似文献
13.
An effective approach for the direct benzylhalogenation with in situ generation of hypervalent halides has been developed.A variety of benzyl halides are produced in moderate to excellent yields(up to 99%) with high regioselectivities.UV absorption spectrum is employed to detect the formation of ferr-butyl hypoiodite. 相似文献
14.
The microwave‐assisted synthesis of diaryl ethers directly from aryl halides and arylmethanesulfonates, which as latent phenols obviate a deprotection step prior to the SNAr reaction, in the presence of Cs2CO3 is described. The reaction time was very short (6–9 min), and good to excellent yields (53–90%) with the wide substrate scope were achieved without any catalyst. 相似文献
15.
Electrochemical bromination of alkyl aromatic compounds by two-phase electrolysis yields the corresponding α, α-dibrominated products. The reaction has been carried out in a single-compartment electrochemical cell using aqueous sodium bromide (40–50%), containing a catalytic amount of HBr as electrolyte, and chloroform, containing an alkyl aromatic compound, as the organic phase with a Pt plate as anode at 10–15°C. Two-phase electrolysis results in high yields (70–90%) of dibromomethyl, bis(bromomethyl), and bis(dibromomethyl) arenes, depending upon the charge passed. 相似文献
16.
Giovanni Appendino Giancarlo Cravotto Giovanni Palmisano Rita Annunziata 《合成通讯》2013,43(18):3359-3371
In the presence of one-electron metal oxidants (CAN, MAH), 4-hydroxycoumarin (1) adds to alkenes to give 2,3-dihydro-4H-furo[3,2-c][1]benzopyran-4-ones. 相似文献
17.
Metal‐Catalyzed Reductive Coupling Reactions of Organic Halides with Carbonyl‐Type Compounds 下载免费PDF全文
Dr. Toni Moragas Dr. Arkaitz Correa Prof. Dr. Ruben Martin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(27):8242-8258
Metal‐catalyzed reductive coupling reactions of aryl halides and (pseudo)halides with carbonyl‐type compounds have undergone an impressive development within the last years. These methodologies have shown to be a powerful alternate strategy, practicality aside, to the use of stoichiometric, well‐defined, and, in some cases, air‐sensitive organometallic species. In this Minireview, the recent findings in this field are summarized, with particular emphasis on the mechanistic interpretation of the results and future aspects of this area of expertise. 相似文献
18.
19.
F
A1:Ag+ color center at the low coordination (100) and (110) surface sites of KCl and KBr thin films play an important role in providing
tunable laser oscillation and adsorbatesubstrate interactions. Double-well potentials at this site are investigated using
ab initio molecular electronic structure calculations. The calculated Stokes shifted (optical transition bands), opticaloptical
conversion efficiencies, the probability of orientational destruction, exciton (energy) transfer and Glasner-Tompkins empirical
rule suggest that laser light generation is sensitive to (i) the lattice anion, (ii) the coordination number of surface ions,
and (iii) the choice of the basis set centered on the anion vacancy. The adsorbate-substrate interactions were found to be
dependent on the electronegativity of the adatom and on the lattice anion. Optimised geometries and the coadsorption of CO
and (F, Cl, Br, I) on KCl and KBr (100) crystals are presented. Calculated chemisorption energies for CO on the (halogen atom/defect
free sites of KCl and KBr (100) crystals) showed that the coadsorption of halogen atom tends to block other adsorbate-substrate
interactions at the nearest neighbour sites. Thus if halogen atom coverage increases, the CO prefers to be adsorbed on the
K+ site of the KCl and KBr (100) surfaces and on KBr relative to KCl.
相似文献
20.