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The reaction of dibenzylmercury with secondary phosphines: phosphorus-phosphorus bond formation versus benzyl substitutionYEH, J. T; AVENS, L. R; MILLS, J. L et al.Phosphorus, sulfur and silicon and the related elements (Print). 1990, Vol 47, Num 3-4, pp 319-323, issn 1042-6507Article

Zur Reaktion von Phosphorverbindungen mit Schwesinger Basen-I P-C-Bindungknüpfung an P-H-Funktionellen Phosphorverbindungen = Reactions of phosphorus compounds with schwesinger bases. I: P-C-binding at P-H- functional phosphorus compoundsUHLIG, F; PUSCHNER, B; HERRMANN, E et al.Phosphorus, sulfur and silicon and the related elements (Print). 1993, Vol 81, Num 1-4, pp 155-163, issn 1042-6507Article

A convenient and facile synthesis of dialkylphosphinesMAJEWSKI, P.Synthesis (Stuttgart). 1987, Num 6, pp 554-555, issn 0039-7881Article

First resolution of a free secondary phosphine chiral at phosphorusBADER, A; PABEL, M; WILD, S. B et al.Journal of the Chemical Society. Chemical communications. 1994, Num 12, pp 1405-1406, issn 0022-4936Article

Investigation of the reaction between dialkylphosphines and carbon tetrachloride. IMAJEWSKI, P.Phosphorus, sulfur and silicon and the related elements (Print). 1993, Vol 85, Num 1-4, pp 41-47, issn 1042-6507Article

Exchange reactions ot tetrakis(trifluoromethyl)diphosphine with pnicogen-pnicogen, phosphorus-hydrogen, and phosphorus-chlorine bondsAVENS, L. R; CRIBBS, L. V; MILLS, J. L et al.Inorganic chemistry (Print). 1989, Vol 28, Num 2, pp 211-214, issn 0020-1669, 4 p.Article

Neue Methoden zur Chlorierung von Organophosphorverbindungen mit P-H Funktionen = Nouvelles méthodes de chloration des composés organiques du phosphore possédant une fonction P-H = New methods for the chlorination of organophosphorus compounds with P-H-functionsWEFERLING, N.Zeitschrift für anorganische und allgemeine Chemie (1950). 1987, Num 548, pp 55-62, issn 0044-2313Article

Oxidative Transition-Metal-Free Cross-Coupling of Secondary Phosphine Chalcogenides and Alcohols or Phenols: A Facile, Expedient Synthesis of Phosphinochalcogenoic O-EstersGUSAROVA, Nina K; VOLKOV, Pavel A; IVANOVA, Nina I et al.Synthesis (Stuttgart). 2011, Num 22, pp 3723-3729, issn 0039-7881, 7 p.Article

Monomeric base-stabilized posphino- and arsinoalanesATWOOD, D. A; CONTRERAS, L; COWLEY, A. H et al.Organometallics. 1993, Vol 12, Num 1, pp 17-18, issn 0276-7333Article

Synthesis and reations of phospine-boranes. Synthesis of new bidentate ligands with homochiral phosphine centers via optically pure phosphine-boranesIMAMOTO, T; OSHIKI, T; ONOZAWA, T et al.Journal of the American Chemical Society. 1990, Vol 112, Num 13, pp 5244-5252, issn 0002-7863Article

Wasser-Abspaltung aus Phosphor-Sauerstoff-Verbindungen: Die Thermolyse von Dimethylphosphanoxid zu 2-Phosphapropen = Elimination d'eau de composés phosphore-oxygène: formation de phospha-2 propène par thermolyse de l'oxyde de diméthylphosphine = Water elimination from phosphorus-oxygen compounds: the formation of 2-phosphapropene by thermolysis of dimethylphosphine oxideBOCK, H; BANKMANN, M.Angewandte Chemie. 1989, Vol 101, Num 7, pp 950-952, issn 0044-8249Article

Unstabilized 1-phosphaallenes : synthesis and characterizationGUILLEMIN, J.-C; JANATI, T; DENIS, J.-M et al.Tetrahedron letters. 1994, Vol 35, Num 2, issn 0040-4039, 190, 245-248 [5 p.]Article

Di-1-Adamantylphosphin, ein Sterisch Hoch Gehindertes Sekundäres Phosphin. Darstellung und Reaktionen = Di-1-adamantylphosphine, a steric hindrance secondary phosphine. Synthesis and reactivityGOERLICH, J. R; SCHMUTZLER, R.Phosphorus, sulfur and silicon and the related elements (Print). 1993, Vol 81, Num 1-4, pp 141-148, issn 1042-6507Article

Reactions of phosphoryl and thiophosphoryl isocyanates and isothiocyanates with secondary amines and phosphinesHERRMANN, E; WILHELM, H; OHMS, G et al.Phosphorus, sulfur and silicon and the related elements (Print). 1993, Vol 75, Num 1-4, pp 111-114, issn 1042-6507Conference Paper

Synthese primärer und sekundärer Phosphane durch selektive Alkylierung von PH3 unter Phasentranferbedingungen = Synthesis of primary and secondary phosphines by alkylation of PH3 under phase transfer conditionsLANGHANS, K. P; STELZER, O; SVARA, J et al.Zeitschrift für Naturforschung. B, A journal of chemical sciences. 1990, Vol 45, Num 2, pp 203-211, issn 0932-0776, 9 p.Article

Darstellung und Eigenschaften von und Reaktionen mit metallhaltigen Heterocyclen. LXVII: Stereochemische Einflüsse auf den Übergang von monomeren Thiophosphinitomangan-Verbindungen (OC)4Mn(η2-S...PR2) zu den dimeren Komplexen [(OC)4Mn(μ-S...PR2)]2 = Préparation, propriétés et réactivité avec des hétérocycles métalliques. LXVII, effets stéréochimiques sur la transformation des composés thiophosphinito monomériques du manganèse (OC)4Mn (η2-S-PR2) en complexes dimériques [(OC)4Mn(μ-S-PR2)]2 = Metal-containing heterocycles: preparation, properties, reactions. LXVII: stereochemical impacts on the transition of monomeric thiophosphinito manganese compounds (OC)4Mn(η2-S-PR2) to the dimeric complexes [(OC)4Mn(μ-S-PR2)]2LINDNER, E; KÄSS, V.Chemische Berichte. 1989, Vol 122, Num 12, pp 2269-2271, issn 0009-2940Article

Synthesis, characterization, and X-ray structure of bis[μ-acetato dicarbonyl(di-tert-butylphosphine)ruthenium(I)]BRIGHT, T. A; JONES, R. A; NUNN, C. M et al.Journal of coordination chemistry. 1988, Vol 18, Num 4, pp 361-367, issn 0095-8972Article

Darstellung und Eignenschaften von und Reaktionen mit Metallhaltigen Heterocyclen. LV: Reduktion von sekundären Phosphankomplexen des Mangans mit K-Selektrid. Ein neuer Weg zu Phosphamanganacylcopropanen = Préparation et propriétés de et réactions avec les hétérocycles contenant un métal. LV. Réduction des complexes de phosphine secondaire de manganèse par le sélectride K; une nouvelle voie aux phosphamanganacyclopropanes = Preparation and properties of and reactions with metal containing heterocycles. LV. Reduction of secondary phosphine complexes of manganese by K selectride; a new way to phosphamanganacyclopropanesLINDNER, E; GOTH, D.Journal of organometallic chemistry. 1987, Vol 319, Num 2, pp 149-160, issn 0022-328XArticle

1-Vinylimidazole : a versatile building block for the synthesis of cationic phosphines useful in ionic liquid biphasic catalysisKOTTSIEPER, Konstantin W; STELZER, Othmar; WASSERSCHEID, Peter et al.Journal of molecular catalysis. A, Chemical. 2001, Vol 175, Num 1-2, pp 285-288, issn 1381-1169Article

Reaktive E=C(p-p)π-Systeme. XXI: Darstellung und Eigenschaften von 1λ3,3λ3-Diphosphanen des Typs R2PCF2P(H)CF3 = Systèmes π E=C(p-p) réactifs. XXI, Préparation et propriétés de diphosphines 1λ3, 3λ3 de type R2PCF2P(H)CF3 = Reactive E=C(p-p) π-Systems. XXI, Preparation and properties of 1λ3, 3λ3-diphosphanes of the type R2PCF2P(H)CF3GROBE, J; LANGE, G; LE VAN, D et al.Zeitschrift für Naturforschung. B, A journal of chemical sciences. 1990, Vol 45, Num 3, pp 299-307, issn 0932-0776Article

Novel anionic chalcogeno ligands. Tellurophosphinites R2PTe- and chalcogenotellurophosphinates R2P(Ch)Te- [Ch=O,S,Se,Te]BILDSTEIN, B; SLADKY, F.Phosphorus, sulfur and silicon and the related elements (Print). 1990, Vol 47, Num 3-4, pp 341-347, issn 1042-6507Article

A simple one-pot synthesis of phosphinoselenoic amides and diamides from secondary phosphine selenides and amines using Et3N-CCl4GUSAROVA, Nina K; VOLKOV, Pavel A; IVANOVA, Nina I et al.Tetrahedron letters. 2011, Vol 52, Num 18, issn 0040-4039, 2279, 2367-2369 [4 p.]Article

Phosphines fonctionnelles alpha-insaturées et alpha-halogénées, nouvelles approches ; réactivité et potentialités synthétiques = Secondary P-vinyl-, P-ethynyl- and P-chloroalkylphosphines ; synthesis, reactivity and synthetic potentialPilard, Jean-François; Denis, J.-M.1994, 186 p.Thesis

Lewis acid promoted reaction of secondary phosphines with carbonyl compounds : remarkalbe effect of niobium(V) chloride in promoting an intramolecular oxidation-reduction procesessSUZUKI, K; HASHIMOTO, T; MAETA, H et al.Synlett. 1992, Num 2, pp 125-128, issn 0936-5214Article

Synthesis of phosphapropyne by flash thermolysis of 1-vinylphosphirane or divinylphosphineHABER, S; LE FLOCH, P; MATHEY, F et al.Journal of the Chemical Society. Chemical communications. 1992, Num 24, pp 1799-1800, issn 0022-4936Article

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