Organophosphorus Chemistry 2018
| dc.contributor.author | Keglevich, György | * |
| dc.date.accessioned | 2021-02-11T21:52:49Z | |
| dc.date.available | 2021-02-11T21:52:49Z | |
| dc.date.issued | 2020 | * |
| dc.date.submitted | 2020-04-07 23:07:08 | * |
| dc.identifier | 44773 | * |
| dc.identifier.uri | https://directory.doabooks.org/handle/20.500.12854/55412 | |
| dc.description.abstract | 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. | * |
| dc.language | English | * |
| dc.subject | QD1-999 | * |
| dc.subject | QD241-441 | * |
| dc.subject | Q1-390 | * |
| dc.subject.classification | thema EDItEUR::P Mathematics and Science::PN Chemistry | en_US |
| dc.subject.other | synergy | * |
| dc.subject.other | 1-(acylamino)alkylphosphonic acids | * |
| dc.subject.other | hydrolytic deacylation | * |
| dc.subject.other | chiral phosphines | * |
| dc.subject.other | organophosphorus chemistry | * |
| dc.subject.other | alcoholysis | * |
| dc.subject.other | electrophilic substitution | * |
| dc.subject.other | NORPHOS | * |
| dc.subject.other | DFT | * |
| dc.subject.other | diphosphines | * |
| dc.subject.other | dry eye syndrome | * |
| dc.subject.other | cyclo-P5 | * |
| dc.subject.other | O-derivatization | * |
| dc.subject.other | triple-decker | * |
| dc.subject.other | phosphorylation | * |
| dc.subject.other | molybdenum | * |
| dc.subject.other | NMR-controlled titration | * |
| dc.subject.other | mechanochemistry | * |
| dc.subject.other | N-acyliminium cation | * |
| dc.subject.other | stability constants | * |
| dc.subject.other | Pudovik reaction | * |
| dc.subject.other | phosphonocarboxylic acids | * |
| dc.subject.other | 1 | * |
| dc.subject.other | aminophosphonic acids | * |
| dc.subject.other | allylic alkylation | * |
| dc.subject.other | diquafosol | * |
| dc.subject.other | silver | * |
| dc.subject.other | Diels-Alder reaction | * |
| dc.subject.other | QTAIM | * |
| dc.subject.other | dissociation constants | * |
| dc.subject.other | weakly coordinating | * |
| dc.subject.other | substitution | * |
| dc.subject.other | phosphonium salts | * |
| dc.subject.other | amino acids | * |
| dc.subject.other | continuous flow reactor | * |
| dc.subject.other | DFT calculations | * |
| dc.subject.other | metallacycle | * |
| dc.subject.other | 31P NMR spectra of intermediates | * |
| dc.subject.other | dinucleotides | * |
| dc.subject.other | N-acylimine | * |
| dc.subject.other | copper | * |
| dc.subject.other | microwave | * |
| dc.subject.other | 1-aminoalkylphosphonic acids | * |
| dc.subject.other | phosphonic acids | * |
| dc.subject.other | bis(phosphane) palladium complex | * |
| dc.subject.other | denufosol | * |
| dc.subject.other | oxidation | * |
| dc.subject.other | C-H bond activation | * |
| dc.subject.other | asymmetric catalysis | * |
| dc.subject.other | dynamic and specific NMR parameters | * |
| dc.subject.other | electronic parameters | * |
| dc.subject.other | dialkyl H-phosphonates | * |
| dc.subject.other | ?-hydroxyphosphonate | * |
| dc.subject.other | transesterification | * |
| dc.subject.other | polycyclic compounds | * |
| dc.subject.other | stereoselective synthesis | * |
| dc.subject.other | rearrangement | * |
| dc.subject.other | hydrolysis | * |
| dc.subject.other | ?-amidoalkylating agents | * |
| dc.subject.other | 3-azaphospholes | * |
| dc.title | Organophosphorus Chemistry 2018 | * |
| dc.type | book | |
| oapen.identifier.doi | 10.3390/books978-3-03928-237-1 | * |
| oapen.relation.isPublishedBy | 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 | * |
| oapen.relation.isbn | 9783039282364 | * |
| oapen.relation.isbn | 9783039282371 | * |
| oapen.pages | 601 | * |
| oapen.edition | 1st | * |
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