Results 121 to 130 of about 12,918 (277)

THE EFFECTS OF ALLYL ETHERS UPON RADICAL POLYMERIZATIONS.

open access: yes, 2001
Three allyl ethers, viz. the ethyl, 2-hydroxyethyl and phenyl compounds, have been examined as additives in radical polymerizations of styrene (STY), methyl methacrylate (MMA) and acrylonitrile (ACN) at 60°C using azobisisobutyronitrile as initiator.
Hunt, B. J.   +3 more
core  

Cinetica da reação de aminolise de 2, 2, 2 - tricloro - 1 - ariletanonas [PDF]

open access: yes, 1988
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciencias Fisicas e MatematicasA cinética da aminólise de 2,2,2-tricloro-1-ariletanonas (1), a 25oC mostra que a ordem da reação em relação às aminas depende do solvente usado ...
Druzian, Janice Izabel
core  

Experimental and theoretical study of the regioselectivity of Claisen rearrangements of substituted allyl phenyl ethers

open access: yes, 2020
Svæðisvendni fyrir Claisen umröðun á nokkrum meta setnum og meta og para setnum allýl phenýl eterum var rannsökuð. Helstu niðurstöður rannsóknarinnar fyrir meta setnu allýl phenýl eterana er að svæðisvendnin veltur gróflega á elektrónískum áhrifum frá ...
William Möller 1989-
core  

Dielectric constant-temperature relationship in some chlorinated phenyl ethers

open access: yes, 1958
Dielectric liquids play an important role in the transmission, distribution, and use of electrical energy. A liquid is arbitrarily classed as a dielectric if its volume resistivity is 10(10) ohm-centimeters or greater.
Martin, Raymond Stuart
core  

1,2-Addition of dimethyl(phenyl)silyllithium to cyclic [alpha],[beta]-unsaturated ketones and regiospecific generation of cyclic silyl enol ethers through brook rearrangement of the 1,2-addition products

open access: yes, 1990
A highly convenient two-step sequence for the regiospecific synthesis of cyclic silyl enol ethers has been developed involving the 1,2-addition of dimethyl(phenyl)silyllithium to cyclic [alpha],[beta]-unsaturated ketones followed by the treatment of the ...
Koo, Sangho   +3 more
core   +1 more source

Toward Chromoselective Transformations in Biological Systems: Perspectives and Challenges

open access: yesAngewandte Chemie International Edition, EarlyView.
Controlling biological systems with small‐molecule chromophores has evolved into a powerful strategy and is applied from chemical biology to medicine. However, the complexity of in vivo systems cannot be matched by a single wavelength of light. Developing methods to combine and individually control multiple chromophores is crucial.
Nadja A. Simeth
wiley   +1 more source

Enantioselective Synthesis of Isoindolinone by Palladium-Catalyzed Aminoalkynylation of O‑Phenyl Hydroxamic Ethers with Alkynes

open access: yes
A highly efficient palladium-catalyzed asymmetric tandem aza-Heck/Sonogashira coupling reaction of O-phenyl hydroxamic ethers with terminal alkynes is described.
Shuaijie Wu (8037842)   +6 more
core   +1 more source

Design, Conformation, and Crystallography of 2-Naphthyl Phenyl Ethers as Potent Anti-HIV Agents. [PDF]

open access: yesACS Med Chem Lett, 2016
Lee WG   +4 more
europepmc   +1 more source

The synthesis and characterization of phosphine functionalized crown ethers by use of spectroscopic and x-ray methods

open access: yes, 1995
The phosphine(III) crown ethers, [4'-(N-phenylaza-15crown-5)]3P (1), [4'-(N-phenylaza-l8-crown-6)]3P (2), [4'-(Naza-18-crown-6)]2-Ph-P (3), and [4'-(benzo-15-crown-5)]3P (4) were synthesized by using an electrophilic bromination of the crown phenyl ring (
Haddadian, Fereshteh
core  

Photogenerated Oxetanes as a Gateway to Uphill Cyclopropanation

open access: yesAngewandte Chemie International Edition, EarlyView.
An atom‐economical route to densely functionalized cyclopropanes from furans and photochemically activated aldehydes is enabled by a unique oxetane‐to‐cyclopropane rearrangement. These cyclopropanes can be used to access complex bioactive scaffolds and serve as a platform for asymmetric cyclopropane synthesis.
Tim Köglmeier   +2 more
wiley   +1 more source

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