نتایج جستجو برای: phenol ortho alkylation

تعداد نتایج: 27115  

Journal: :Chemical communications 2010
Estelle Bellamy Omar Bayh Christophe Hoarau Francois Trécourt Guy Quéguiner Francis Marsais

Ortho-directed functionalisation of arenes using lithium alkylmagnesate bases were achieved, demonstrating the potential use of arylmagnesates as suitable arylanions, without a further transmetallation step, for challenging functionalizations such as fluorination, hydroxylation, arylation, vinylation and alkylation through epoxide ring-opening.

Journal: :Physical chemistry chemical physics : PCCP 2016
Olha Krechkivska Callan M Wilcox Tyler P Troy Klaas Nauta Bun Chan Rebecca Jacob Scott A Reid Leo Radom Timothy W Schmidt Scott H Kable

The reaction of H + phenol and H/D + toluene has been studied in a supersonic expansion after electric discharge. The (1 + 1') resonance-enhanced multiphoton ionization (REMPI) spectra of the reaction products, at m/z = parent + 1, or parent + 2 amu, were measured by scanning the first (resonance) laser. The resulting spectra are highly structured. Ionization energies were measured by scanning ...

Journal: :Organic letters 2007
Barry M Trost Kalindi Dogra

[reaction: see text] Delta9-THC is synthesized in enantiomericaly pure form, where all of the stereochemistry is derived from the molybdenum-catalyzed asymmetric alkylation reaction of the extremely sterically congested bis-ortho-substituted cinnamyl carbonate in high regio- and enantioselectivity.

Journal: :The Journal of organic chemistry 2006
Daniel K Whelligan Carsten Bolm

Syntheses of three regioisomers of aromatic-substituted phosphinyl-oxazolinyl-[2.2]paracyclophanes, pseudo-geminal, pseudo-ortho, and ortho, have been carried out or, in the latter two cases, newly developed. It has, therefore, been demonstrated that all aromatic-substituted isomers relevant for use as chelating ligands for asymmetric catalysis are accessible. These P,N-ligands, along with thei...

Journal: :Tetrahedron 2021

The alkylation of a variety ketones using 1° or 2° alcohols under hydrogen borrowing catalysis is described. Initial research focused on the ?-alkylation cyclopropyl with higher (i.e. larger than MeOH), leading to formation ?-branched products. Our search for additional substrates which explore this chemistry led us discover that di- ortho -substituted aryl were also privileged scaffolds, Ph? (...

2011
MEHDI VADI

Present research paper deals with the adsorption isotherms rate 2-amino phenol and 4-amino phenol on multi-wall carbon nanotube which performed by changing the amount of solution concentration in ppm unit. According to difference between two under studied substances are in substitution of NH2 in ortho and para position , more adsorption of 4-aminophenol on carbon nanotube demonstrate that para ...

Journal: :Journal of The Japan Petroleum Institute 1965

Journal: :Bulletin of the Chemical Society of Japan 1988

Journal: :Chemical communications 2006
Zhirong Zhao Josef Messinger Uwe Schön Rudolf Wartchow Holger Butenschön

Tricarbonylchromium complexes of aryl triflates undergo base-mediated anionic thia-Fries rearrangements to generate push-pull substituted [ortho-hydroxyaryl(trifluoromethylsulfonyl)phenol]tricarbonylchromium complexes under very mild reaction conditions.

Journal: :progress in biological sciences 2011
mohammad reza soudi narjes kolahchi

biodegradation of phenol is a major focus of toxic organic compound degradation by microorganisms isolated from polluted areas. an increasing number of bacteria and fungi possessing unique biodegradation capabilities have been isolated in recent years. in this study a new isolate, rhodococcus erythropolis sko-1, from polluted soils in the tehran oil refinery region, is reported. identificati...

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