LEADER 04873nam 2200457 450 001 9910583094403321 005 20180603084525.0 010 $a0-12-813835-1 010 $a0-12-813834-3 035 $a(CKB)4100000000449568 035 $a(MiAaPQ)EBC5041614 035 $a(PPN)226416194 035 $a(EXLCZ)994100000000449568 100 $a20171012h20182018 uy 0 101 0 $aeng 135 $aurcnu|||||||| 181 $2rdacontent 182 $2rdamedia 183 $2rdacarrier 200 10$aReactivity of P-H group of phosphorus based compounds /$fKolio D. Troev 210 1$aLondon, [England] :$cAcademic Press,$d2018. 210 4$d©2018 215 $a1 online resource (465 pages) 311 08$aOnline version: Troev, Kolio D., author. Reactivity of P-H group of phosphorus based compounds. London, United Kingdom : Academic Press, [2018] 9780128138359 (OCoLC)1003284632 320 $aIncludes bibliographical references at the end of each chapters and index. 327 $aFront Cover; Reactivity of P-H Group of Phosphorus Based Compounds; Copyright Page; Contents; About the Author; Preface; 1 Acidity and Tautomerization of P-H Group; 1.1 Acidity; 1.2 Tautomerization; 1.2.1 Tautomerization of Phosphine Oxides; 1.2.2 Tautomerization of Hypophosphorous Acid; 1.2.3 Tautomerization of H-Phosphinic Acid; 1.2.4 Tautomerization of H-Phosphonic Acid; References; 2 Reactivity of P-H Group of Phosphines; 2.1 Phosphine; 2.1.1 Methods for Preparation; 2.1.2 Reactivity of P-H Group; 2.1.2.1 Reaction with Metals; 2.1.2.2 Addition Reactions 327 $a2.1.2.2.1 Addition to Carbon-Carbon Multiple BondsRadical Addition; Nucleophilic Addition; Catalyzed Hydrophosphination; 2.1.2.2.2 Addition to Carbonyl Group; 2.1.2.3 Nucleophilic Substitution Reactions; 2.2 Primary Phosphines (RPH2); 2.2.1 Methods for Preparation; 2.2.2 Reactivity of P-H Group; 2.2.2.1 Addition Reactions; 2.2.2.1.1 Addition to Carbon-Carbon Multiple Bonds; 2.2.2.1.2 Addition to Carbonyl Group; 2.2.2.2 Cross-Coupling Reactions; 2.2.2.3 Cross-Dehydrogenative Coupling; 2.3 Primary Diphosphines; 2.3.1 Methods for Preparation; 2.3.2 Reactivity of P-H Group; 2.3.2.1 Metalation 327 $a2.5.2 Reactivity of P-H Group2.5.2.1 Condensation Reactions; 2.5.2.2 Cross-Coupling Reactions; 2.5.2.2.1 Diphenyldiphosphine PhHP-PHPh; 2.5.2.2.2 Tetraphenyldiphosphane; 2.6 Phosphine-Borane Complexes; 2.6.1 Phosphine-Borane; 2.6.1.1 Methods for Preparation; 2.6.2 Primary Phosphine-Boranes; 2.6.2.1 Methods for Preparation; 2.6.2.2 Reactivity of P-H Group; 2.6.2.2.1 Hydrophosphination; 2.6.2.2.2 Oxidative Addition; 2.6.2.2.3 Cross-Dehydrogenative Coupling; 2.6.2.2.4 Alkylation; 2.6.3 Secondary Phosphine-Boranes; 2.6.3.1 Methods for Preparation; 2.6.3.2 Reactivity of P-H Group 327 $a2.6.3.2.1 Alkylation2.6.3.2.2 Hydrophosphination; 2.6.3.2.3 Nucleophilic Substitutions; 2.6.3.2.4 Cross-Coupling Reactions; 2.6.3.2.5 Cross-Dehydrogenative Coupling; Poly(phosphinoborane)s; 2.7 Conclusion; References; 3 Reactivity of P-H Group of Phosphine Oxides; 3.1 Phosphine Oxide; 3.1.1 Methods for Preparation; 3.1.2 Reactivity of P-H Group; 3.2 Primary Phosphine Oxides; 3.2.1 Methods for Preparation; 3.2.2 Reactivity of P-H Group; 3.2.2.1 Dehydration; 3.2.2.2 Addition Reactions; 3.2.2.2.1 Addition to Carbon-Carbon Multiple Bonds; 3.3 Secondary Phosphine Oxides 330 $aReactivity of P-H Group of Phosphorus Based Compounds bridges the gap between inorganic and organic phosphorus compounds, providing a basis to explore the myriad possibilities for synthesis of novel low and high molecular phosphorus-containing compounds. It covers well-documented reactions in detail, including: tautomerization, oxidation, reduction, alkylation, oxidation coupling, addition reaction to: carbon-carbon multiple bonds, Schiff base, isocyanates, nitriles, epoxides; addition to carbonyl group, Kabachnik- Fields reaction, cross-coupling reaction and more. In an accessible style complete with synthetic routes and figures, the resource then covers the reactivity of multiple P-H group members: phosphines, phosphine oxides, hypophosphorus acid, H-phosphinic acids and polys(alkylene H-phosphonate). This valuable coverage supports the advancement of research and applications in this area for scientists solving a scientific problem or starting a variety of new projects, such as a new reaction for the synthesis of biologically active compounds, new methods of polymer synthesis or a new methodology for polymer modification. 606 $aPhosphorus compounds 615 0$aPhosphorus compounds. 676 $a546.712 700 $aTroev$b Kolio D.$0897328 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910583094403321 996 $aReactivity of P-H group of phosphorus based compounds$92004735 997 $aUNINA LEADER 01802nam 2200421 450 001 9910163205203321 005 20170816133812.0 010 $a1-78289-443-8 035 $a(CKB)3710000001046270 035 $a(MiAaPQ)EBC4809012 035 $a(OCoLC)843300850$z(OCoLC)844590702 035 $a(EXLCZ)993710000001046270 100 $a20200109h20132009 uy 0 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aClose air support and the Battle for Khe Sanh /$fShawn Callahan 210 1$a[Place of publication not identified] :$cPickle Partners Publishing,$d2013. 210 4$d©2009 215 $a1 online resource (220 pages) 225 1 $aOccasional paper 300 $aTitle from title screen (viewed Aug. 5, 2013). 320 $aIncludes bibliographical references (pages 155-179). 327 $aClose air support doctrines -- Khe Sanh background -- The Hill Battles of 1967 -- The Siege of 1968 -- Operation Pegasus and the relief of Khe Sanh -- The Deep air battle and the B-52 -- Radar controlled tactical air support -- Close air support -- Conclusions -- Appendix A. Glossary of acronyms and terms -- Appendix B. Orders of Battle -- Appendix C. Fratricide and near fratricide aviations incidents at Khe Sanh. 606 $aVietnam War, 1961-1975$xAerial operations, American 615 0$aVietnam War, 1961-1975$xAerial operations, American. 676 $a959.704348 700 $aCallahan$b Shawn$01352795 712 02$aMarine Corps University (U.S.).$bHistory Division, 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910163205203321 996 $aClose air support and the Battle for Khe Sanh$93201959 997 $aUNINA LEADER 00945nam a2200217 i 4500 001 991004364034507536 005 20250127150559.0 008 250127s1990 it a er 000 0 ita d 040 $aBibl. Dip.le Aggr. Ingegneria Innovazione - Sez. IngegneriaInnovazione$beng$cSocioculturale Scs 041 0 $aita 082 04$a539.73$223. 100 1 $aCagliolti, Giuseppe$01783397 245 10$aScattering anelastico dei neutroni e stabilità meccanica dei materiali ; Teoria dello scattering anelastico dei neutroni /$cGiuseppe Caglioti 260 $a[S.l.] :$b[s.n.],$c1990 300 $a1 volume (various pagings) :$bill. ;$c29 cm 500 $aTitle and statement of responsability taken from cover 500 $aTypescript 650 4$aNeutron scattering 912 $a991004364034507536 996 $aScattering anelastico dei neutroni e stabilità meccanica dei materiali ; Teoria dello scattering anelastico dei neutroni$94310965 997 $aUNISALENTO LEADER 01166nas 2200361 c 450 001 9910896176703321 005 20251012104835.0 035 $a(DE-599)ZDB3182388-9 035 $a(OCoLC)1429553950 035 $a(DE-101)1323854037 035 $a(CKB)5860000000505382 035 $a(EXLCZ)995860000000505382 100 $a20240319a20189999 |y | 101 0 $ager 135 $aur||||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aJahresbericht ..$eScience in Focus$fFraunhofer-Institut fu?r Angewandte Optik und Feinmechanik IOF = Annual report ... : Science in focus / Fraunhofer Insitute for Applied Optics and Precision Engineering IOF 210 31$aJena$cFraunhofer-Institut fu?r Angewandte Optik und Feinmechanik IOF$d[2018]- 215 $aOnline-Ressource 300 $aGesehen am 19.03.2024 517 $aJahresbericht ... 608 $aZeitschrift$2gnd-content 608 $aBericht$2gnd-content 676 $a530 801 0$b0027 801 1$bDE-101 801 2$b9999 906 $aJOURNAL 912 $a9910896176703321 996 $aJahresbericht$9415024 997 $aUNINA