Organophosphorus Chemistry 2018

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 starting materials or intermediates in syntheses....

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Main Author: Keglevich, György (auth)
Format: Electronic Book Chapter
Language:English
Published: MDPI - Multidisciplinary Digital Publishing Institute 2020
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245 1 0 |a Organophosphorus Chemistry 2018 
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520 |a 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 starting materials or intermediates in syntheses. Let us mention the Wittig reaction and the related transformations, the Arbuzov- and the Pudovik reactions, the Kabachnik-Fields condensation, the Hirao reaction, the Mitsunobu reaction, etc. Other reactions, e.g., homogeneous catalytic transformations or C-C coupling reactions involve P-ligands in transition metal (Pt, Pd, etc.) complex catalysts. The synthesis of chiral organophosphorus compounds means a continuous challenge. Methods have been elaborated for the resolution of tertiary phosphine oxides and for stereoselective organophosphorus transformations. P-heterocyclic compounds, including aromatic and bridged derivatives, P-functionalized macrocycles, dendrimers and low coordinated P-fragments, are also of interest. An important segment of organophosphorus chemistry is the pool of biologically-active compounds that are searched and used as drugs, or as plant-protecting agents. The natural analogue of P-compounds may also be mentioned. Many new phosphine oxides, phosphinates, phosphonates and phosphoric esters have been described, which may find application on a broad scale. Phase transfer catalysis, ionic liquids and detergents also have connections to phosphorus chemistry. Green chemical aspects of organophosphorus chemistry (e.g., microwave-assisted syntheses, solvent-free accomplishments, optimizations, and atom-efficient syntheses) represent a dynamically developing field. Last, but not least, theoretical approaches and computational chemistry are also a strong sub-discipline within organophosphorus chemistry. 
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650 7 |a Chemistry  |2 bicssc 
653 |a synergy 
653 |a 1-(acylamino)alkylphosphonic acids 
653 |a hydrolytic deacylation 
653 |a chiral phosphines 
653 |a organophosphorus chemistry 
653 |a alcoholysis 
653 |a electrophilic substitution 
653 |a NORPHOS 
653 |a DFT 
653 |a diphosphines 
653 |a dry eye syndrome 
653 |a cyclo-P5 
653 |a O-derivatization 
653 |a triple-decker 
653 |a phosphorylation 
653 |a molybdenum 
653 |a NMR-controlled titration 
653 |a mechanochemistry 
653 |a N-acyliminium cation 
653 |a stability constants 
653 |a Pudovik reaction 
653 |a phosphonocarboxylic acids 
653 |a 1 
653 |a aminophosphonic acids 
653 |a allylic alkylation 
653 |a diquafosol 
653 |a silver 
653 |a Diels-Alder reaction 
653 |a QTAIM 
653 |a dissociation constants 
653 |a weakly coordinating 
653 |a substitution 
653 |a phosphonium salts 
653 |a amino acids 
653 |a continuous flow reactor 
653 |a DFT calculations 
653 |a metallacycle 
653 |a 31P NMR spectra of intermediates 
653 |a dinucleotides 
653 |a N-acylimine 
653 |a copper 
653 |a microwave 
653 |a 1-aminoalkylphosphonic acids 
653 |a phosphonic acids 
653 |a bis(phosphane) palladium complex 
653 |a denufosol 
653 |a oxidation 
653 |a C-H bond activation 
653 |a asymmetric catalysis 
653 |a dynamic and specific NMR parameters 
653 |a electronic parameters 
653 |a dialkyl H-phosphonates 
653 |a ?-hydroxyphosphonate 
653 |a transesterification 
653 |a polycyclic compounds 
653 |a stereoselective synthesis 
653 |a rearrangement 
653 |a hydrolysis 
653 |a ?-amidoalkylating agents 
653 |a 3-azaphospholes 
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