Show simple item record

dc.contributor.authorKeglevich, György*
dc.date.accessioned2021-02-11T21:52:49Z
dc.date.available2021-02-11T21:52:49Z
dc.date.issued2020*
dc.date.submitted2020-04-07 23:07:08*
dc.identifier44773*
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/55412
dc.description.abstractOrganophosphorus 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.languageEnglish*
dc.subjectQD1-999*
dc.subjectQD241-441*
dc.subjectQ1-390*
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PN Chemistryen_US
dc.subject.othersynergy*
dc.subject.other1-(acylamino)alkylphosphonic acids*
dc.subject.otherhydrolytic deacylation*
dc.subject.otherchiral phosphines*
dc.subject.otherorganophosphorus chemistry*
dc.subject.otheralcoholysis*
dc.subject.otherelectrophilic substitution*
dc.subject.otherNORPHOS*
dc.subject.otherDFT*
dc.subject.otherdiphosphines*
dc.subject.otherdry eye syndrome*
dc.subject.othercyclo-P5*
dc.subject.otherO-derivatization*
dc.subject.othertriple-decker*
dc.subject.otherphosphorylation*
dc.subject.othermolybdenum*
dc.subject.otherNMR-controlled titration*
dc.subject.othermechanochemistry*
dc.subject.otherN-acyliminium cation*
dc.subject.otherstability constants*
dc.subject.otherPudovik reaction*
dc.subject.otherphosphonocarboxylic acids*
dc.subject.other1*
dc.subject.otheraminophosphonic acids*
dc.subject.otherallylic alkylation*
dc.subject.otherdiquafosol*
dc.subject.othersilver*
dc.subject.otherDiels-Alder reaction*
dc.subject.otherQTAIM*
dc.subject.otherdissociation constants*
dc.subject.otherweakly coordinating*
dc.subject.othersubstitution*
dc.subject.otherphosphonium salts*
dc.subject.otheramino acids*
dc.subject.othercontinuous flow reactor*
dc.subject.otherDFT calculations*
dc.subject.othermetallacycle*
dc.subject.other31P NMR spectra of intermediates*
dc.subject.otherdinucleotides*
dc.subject.otherN-acylimine*
dc.subject.othercopper*
dc.subject.othermicrowave*
dc.subject.other1-aminoalkylphosphonic acids*
dc.subject.otherphosphonic acids*
dc.subject.otherbis(phosphane) palladium complex*
dc.subject.otherdenufosol*
dc.subject.otheroxidation*
dc.subject.otherC-H bond activation*
dc.subject.otherasymmetric catalysis*
dc.subject.otherdynamic and specific NMR parameters*
dc.subject.otherelectronic parameters*
dc.subject.otherdialkyl H-phosphonates*
dc.subject.other?-hydroxyphosphonate*
dc.subject.othertransesterification*
dc.subject.otherpolycyclic compounds*
dc.subject.otherstereoselective synthesis*
dc.subject.otherrearrangement*
dc.subject.otherhydrolysis*
dc.subject.other?-amidoalkylating agents*
dc.subject.other3-azaphospholes*
dc.titleOrganophosphorus Chemistry 2018*
dc.typebook
oapen.identifier.doi10.3390/books978-3-03928-237-1*
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0*
oapen.relation.isbn9783039282364*
oapen.relation.isbn9783039282371*
oapen.pages601*
oapen.edition1st*


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

https://creativecommons.org/licenses/by-nc-nd/4.0/
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/