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....
Saved in:
Main Author: | |
---|---|
Format: | Electronic Book Chapter |
Language: | English |
Published: |
MDPI - Multidisciplinary Digital Publishing Institute
2020
|
Subjects: | |
Online Access: | DOAB: download the publication DOAB: description of the publication |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
MARC
LEADER | 00000naaaa2200000uu 4500 | ||
---|---|---|---|
001 | doab_20_500_12854_55412 | ||
005 | 20210211 | ||
003 | oapen | ||
006 | m o d | ||
007 | cr|mn|---annan | ||
008 | 20210211s2020 xx |||||o ||| 0|eng d | ||
020 | |a books978-3-03928-237-1 | ||
020 | |a 9783039282364 | ||
020 | |a 9783039282371 | ||
040 | |a oapen |c oapen | ||
024 | 7 | |a 10.3390/books978-3-03928-237-1 |c doi | |
041 | 0 | |a eng | |
042 | |a dc | ||
072 | 7 | |a PN |2 bicssc | |
100 | 1 | |a Keglevich, György |4 auth | |
245 | 1 | 0 | |a Organophosphorus Chemistry 2018 |
260 | |b MDPI - Multidisciplinary Digital Publishing Institute |c 2020 | ||
300 | |a 1 electronic resource (601 p.) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
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. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by-nc-nd/4.0/ |2 cc |4 https://creativecommons.org/licenses/by-nc-nd/4.0/ | ||
546 | |a English | ||
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 | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/2050 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/55412 |7 0 |z DOAB: description of the publication |