Results 21 to 30 of about 2,325,545 (220)

The bis(Biphenyl)phosphorus Fragment in Trivalent and Tetravalent P-Environments

open access: yesInorganics, 2021
Diaryl substituted phosphorus (III) compounds are commonly used motifs in synthesis. Although the basic synthetic routes to these molecules starting from PCl3 are well reported, sterically hindered aryl substituents can be difficult to introduce ...
Jonas Hoffmann   +3 more
doaj   +1 more source

One-Pot Phosphonylation of Heteroaromatic Lithium Reagents: The Scope and Limitations of Its Use for the Synthesis of Heteroaromatic Phosphonates

open access: yesMolecules, 2023
A one-pot lithiation–phosphonylation procedure was elaborated as a method to prepare heteroaromatic phosphonic acids. It relied on the direct lithiation of heteroaromatics followed by phosphonylation with diethyl chlorophosphite and then oxidation with ...
Ewa Chmielewska   +4 more
doaj   +1 more source

Synthesis of Mixed Arylalkyl Tertiary Phosphines via the Grignard Approach

open access: yesMolecules, 2022
Trialkyl and triaryl phosphines are important classes of ligands in the field of catalysis and materials research. The wide usability of these low-valent phosphines has led to the design and development of new synthesis routes for a variety of phosphines.
Ashanul Haque   +4 more
doaj   +1 more source

Organophosphorus Chemistry 2018

open access: yes, 2020
Organophosphorus chemistry is an important discipline within organic chemistry. Phosphorus compounds, such as phosphines, trialkyl phosphites, phosphine oxides (chalcogenides), phosphonates, phosphinates and >P(O)H species, etc., may be important ...
Keglevich, György
core   +1 more source

Isolatable organophosphorus(III)-tellurium heterocycles [PDF]

open access: yes, 2014
We are grateful to the University of St Andrews, the EPSRC and NSERC Canada for their financial support.A new structural arrangement Te3(RPIII)3 and the first crystal structures of organophosphorus(III)–tellurium heterocycles are presented.
Woollins, J. Derek   +8 more
core   +1 more source

A-series (“Novichok”) nerve agents: Chemistry, toxicology, detection, and medical countermeasures [PDF]

open access: yesPharmacia
Available evidence indicates that A-series (“Novichok”) nerve agents are highly toxic organophosphorus compounds whose primary mechanism of action involves potent inhibition of acetylcholinesterase, resulting in severe cholinergic toxicity and ...
Ahmed Nedzhib   +3 more
doaj   +3 more sources

A structural, spectroscopic and theoretical study of the triphenylphosphine chalcogenide complexes of tungsten carbonyl, [W(XPPh3)(CO)5], X=O, S, Se [PDF]

open access: yes, 2004
The series [W(XPPh3)(CO)5], X=O, S, Se has been structurally determined by X-ray crystallography and fully characterised spectroscopically to provide data for comparing the bonding of the Ph3PX ligands to the metal.
Nicholson, Brian K.   +2 more
core   +1 more source

Homolytic substitution at phosphorus for C–P bond formation in organic synthesis

open access: yesBeilstein Journal of Organic Chemistry, 2013
Organophosphorus compounds are important in organic chemistry. This review article covers emerging, powerful synthetic approaches to organophosphorus compounds by homolytic substitution at phosphorus with a carbon-centered radical. Phosphination reagents
Hideki Yorimitsu
doaj   +1 more source

Enhancing Paraoxon Binding to Organophosphorus Hydrolase Active Site [PDF]

open access: yes, 2021
Organophosphorus (OP) compounds are among the most toxic of chemical substances and widely used as insecticides, pesticides, and chemical warfare agents. The most important enzyme inhibited by OP compounds is acetylcholinesterase (AChe).
David, Mobley   +3 more
core   +2 more sources

Assessment of the Equilibrium Constants of Mixed Complexes of Rare Earth Elements with Acidic (Chelating) and Organophosphorus Ligands

open access: yesSeparations, 2022
A survey of the experimental equilibrium constants in solution for the mixed complexes of 4f ions with acidic (chelating) and O-donor organophosphorus ligands published in the period between 1954 and 2022 is presented.
Maria Atanassova
doaj   +1 more source

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