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Journal articles on the topic 'C.A.P. Scornicești'

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Published: 4 June 2021

Last updated: 29 July 2025

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1

Hietkamp, Sibbele, Thomas Lebbe, Gerd U. Spiegel, and Othmar Stelzer. "Oligophosphaalkane, XVII Funktionalisierte Tri-, Tetra-und Pentaphosphaalkane mit der Donorsequenz P-C-C-P und P-C-C-C-P/Oligophosphaalkanes, XVII Functionalized Tri-, Tetra-and Pentaphosphaalkanes with the Donor Sequence P-C-C-P and P-C-C-C-P." Zeitschrift für Naturforschung B 42, no. 2 (1987): 177–85. http://dx.doi.org/10.1515/znb-1987-0210.

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Abstract Starting with the secondary phosphanes R2PH (R = Me, Ph, iPr) and the vinyl-or allylmethylphosphinic acid isopropylesters, the triphosphaalkanes R2P-[CH2]3 -PMe -[CH2]2 -PMeH containing one terminal PH-group have been synthesized in a multiple step synthesis. The tertiary-secondary phosphanes R2P-[CH2]3 -PMeH obtained as intermediates may be used for the syntheses of hybrid donor systems PPN. The P-C-skeletons of the tetra-and pentadentate oligophosphaalkanes have been built up by a free radical initiated addition of the vinyl or allyl compounds CH2=CH-P(NEt2)2 or CH2 =CH-CH2-P(O)(OiP

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2

Pol, Roman. "On metrizable E with C p ( E ) ≇ C p ( E ) × C p ( E )." Mathematika 42, no. 1 (1995): 49–55. http://dx.doi.org/10.1112/s0025579300011347.

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3

Krupski, Mikołaj, and Witold Marciszewski. "A metrizable X with C p (X) not homeomorphic to C p (X) × C p (X)." Israel Journal of Mathematics 214, no. 1 (2016): 245–58. http://dx.doi.org/10.1007/s11856-016-1373-y.

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4

Schlapp-Hackl, Inge, Christoph Falschlunger, Kathrin Zauner та ін. "Syntheses and crystal structures of [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}ClH]Cl·2.75CH2Cl2 and its derivatives, [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}(CH2CO2Et)Cl]Cl·CH3OH·0.5H2O, [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}Cl2]Cl·CH3OH·2H2O and [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}(CH2CO2Et)(CO)]Cl2·2CH2Cl2·1.5H2O". Acta Crystallographica Section E Crystallographic Communications 75, № 1 (2019): 12–20. http://dx.doi.org/10.1107/s2056989018017024.

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The common feature of the four iridium(III) salt complexes, (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)chloridohydridoiridium(III) chloride methylene chloride 2.75-solvate (4), (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)chlorido(ethoxyoxoethanido)iridium(III) chloride–methanol–water (1/1/0.5) (5), (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)dichloridoiridium(III) chloride–methanol–water (1/1/2) (6) and (bis{[(diphenylphosph

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5

Karsch, Hans H., Brigitte Deubelly, Gregor Grauvogl, and Gerhard Müller. "Oxidative Verknüpfung von Phosphinomethanidliganden an Titanocen- und Bismutzentren: selektive CC-, PC- und PP-Bindungsbildung." Journal of Organometallic Chemistry 459, no. 1-2 (1993): 95–105. http://dx.doi.org/10.1016/0022-328x(93)86060-u.

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6

Yoshifuji, Masaaki. "Chemistry of Several Sterically Bulky Molecules with P=P, P=C, and C≡P Bond." Molecules 27, no. 5 (2022): 1557. http://dx.doi.org/10.3390/molecules27051557.

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Several sterically protected, low-coordinate organophosphorus compounds with P=P, P=C, and C≡P bond are described in this study. Molecules such as diphosphenes, phosphaalkenes, 1-phosphaallenes, 1,3-diphosphaallenes, 3,4-diphosphinidenecyclobutenes, and phosphaalkynes are stabilized with an extremely bulky 2,4,6-tri-t-butylphenyl (Mes*) group. The synthesis, structures, physical, and chemical properties of these molecules are discussed, together with some successful applications in catalytic organic reactions.

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7

Frances, Mary. "Glossary. The C-P-C cycle." Rivista Italiana Costruttivismo 6, no. 2 (2018): 61–63. http://dx.doi.org/10.69995/pqwp4764.

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8

Wesseling, Rein. "Joined Cases C-238/99 P, C-244/99 P, C-245/99 P, C-247/99 P, C-250/99 P to C-252/99 P and C-254/99 P, Limburgse Vinyl Maatschappij NV (LVM) and Others v. Commission, [2002] ECR 1-8375." Common Market Law Review 41, Issue 4 (2004): 1141–55. http://dx.doi.org/10.54648/cola2004039.

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9

KNAZIK, STEPHEN R. "P EDIATRIC P REHOSPITAL C ARE." Prehospital Emergency Care 6, no. 4 (2002): 478. http://dx.doi.org/10.1080/10903120290938210.

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10

Castillo, F. "P? A? E? C?-E? P?" Computers & Chemical Engineering 19, no. 1 (1995): S89—S94. http://dx.doi.org/10.1016/0098-1354(95)00157-w.

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11

Grobe, Joseph, Duc Le Van та Thomas Großpietsch. "Reaktive E=C(p-p)π-Systeme, XXVIII / Reactive E=C(p-p)π-Systems, XXVIII". Zeitschrift für Naturforschung B 46, № 8 (1991): 978–84. http://dx.doi.org/10.1515/znb-1991-0802.

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The reaction of perfluoro-2-phosphapropene F3CP=CF2 (1) with tert-butylamine or isopropylamine in a 1:3 molar ratio leads to the novel iminomethylene phosphanes F3CP=C=N(tBu) [(2), 30% yield] and F3CP=C=N(iPr) [(3), 5%], respectively. 2 slowly decomposes at room temperature giving tert-butylisonitrile and the cyclophosphanes (F3CP)n (n = 3, 4, 5). 3 is found to be less stable than 2 and for example is attacked by primary amines. The reaction of 2 with 2,3-dimethyl-1,3-butadiene or trimethylphosphane yields, on the one hand, the cycloaddition product of bis(trifluormethyl)diphosphene (4), and o

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12

Albers, Thomas, Joseph Grobe, Duc Le Van, Bernt Krebs та Mechtild Läge. "Reaktive E=C (p-p)π-Systeme, XL. / Reactive E=C(p-p)π Systems, XL." Zeitschrift für Naturforschung B 50, № 1 (1995): 94–100. http://dx.doi.org/10.1515/znb-1995-0119.

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The reaction of bis(trifluoromethyl)arsane 2 with secondary amines R2NH in a molar ratio of 1:3 at -60 °C allows the preparation of trifluoromethyl arsaalkenes of the type F3CAs=C(F)NR2 in moderate yields (15-35%) [NR2 = NMe2 (3a), NMeEt (3b), NEt2 (3c)]. The main product of the reaction of 2 with Me2NH is the 1,1-diamino compound F3CAs=C(NMe2)2 (4a). With ethyl(isopropyl)- or di(isopropyl)amine the corresponding derivatives F3CAs=C(F)NEt(iPr) (3d) and F3CAs=C(F)N(iPr)2 (3e), respectively, are formed only in traces (3d), or not at all (3 e). However, 3d and 3e can be prepared by reacting perfl

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13

Escudié, Jean, and Gabriela Nemeş. "Phosphasilaallenes >Si=C=P− and phosphagermaallenes >Ge=C=P−." Comptes Rendus Chimie 13, no. 8-9 (2010): 954–63. http://dx.doi.org/10.1016/j.crci.2010.03.012.

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14

Pietraszko, J., G. Agakishiev, C. Agodi, et al. "DIELECTRON PRODUCTION IN C + C AND p + p COLLISIONS WITH HADES." International Journal of Modern Physics A 22, no. 02n03 (2007): 388–96. http://dx.doi.org/10.1142/s0217751x07035574.

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The High Acceptance Di-Electron Spectrometer HADES1 has been constructed at the SIS accelerator (GSI Darmstadt) to investigate electron-positron pairs produced in proton, pion and heavy ion induced reactions. The main goal of these studies is to explore properties of hadrons in nuclear matter. The apparatus and the experimental results from C + C at 2.0 AGeV and 1.0 AGeV and p + p at 2.2 GeV compared with Monte-Carlo events from a generator based on known cross-sections and branching ratios are presented.

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15

MCGEORGE, FRANK. "C OMMON H AND P ROBLEMS IN P RIMARY C ARE." Prehospital Emergency Care 4, no. 2 (2000): 199. http://dx.doi.org/10.1080/10903120090941515.

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16

McClard, Ronald W., Thomas S. Fujita, Kay E. Stremler, and C. Dale Poulter. "Novel phosphonylphosphinyl (P-C-P-C-) analogs of biochemically interesting diphosphates. Syntheses and properties of P-C-P-C-, analogs of isopentenyl diphosphate and dimethylallyl diphosphate." Journal of the American Chemical Society 109, no. 18 (1987): 5544–45. http://dx.doi.org/10.1021/ja00252a051.

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17

Nordlander, Kristina. "Joined Cases C-189/02 P, C-202/02 P, C-205/02 P to C-208/02 P and C-213/02 P, Dansk Rørindustri and others v. Commission." Common Market Law Review 43, Issue 2 (2006): 571–82. http://dx.doi.org/10.54648/cola2006002.

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18

Yang, Chengmin. "Projections $P$ on $C=C[-1,1]$ which interpolate at $\dim (P(C))$ or more points." Proceedings of the American Mathematical Society 115, no. 3 (1992): 669. http://dx.doi.org/10.1090/s0002-9939-1992-1089415-4.

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19

Rhainds, Marc, Edward G. Kettela, and Peter J. Silk. "C. P. Alexander review." Canadian Entomologist 144, no. 3 (2012): 379–95. http://dx.doi.org/10.4039/tce.2012.18.

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AbstractThe Canadian registration in 2007 of Disrupt SBW Micro-Flakes®, a pheromone-based product for control of spruce budworm,Choristoneura fumiferana(Clemens), paved the way for large-scale trials to test the practicality of mating disruption as a commercial pest management strategy. We review results from field and laboratory experiments on pheromone-based mating disruption of spruce budworm conducted from 1974 to 2008. Application of pheromone from the ground or the air consistently reduced the orientation of males toward pheromone sources. Mating disruption also reduced the mating succes

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20

Papalexakis, Evangelos E., Christos Faloutsos, and Nicholas D. Sidiropoulos. "P ar C ube." ACM Transactions on Knowledge Discovery from Data 10, no. 1 (2015): 1–25. http://dx.doi.org/10.1145/2729980.

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21

Thomas, R. S. "P. C. Wren'sBeau Geste." Children's Literature in Education 21, no. 4 (1990): 209–17. http://dx.doi.org/10.1007/bf01466545.

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22

Petrar, Petronela Maria, Gabriela Nemes, Ioan Silaghi-Dumitrescu, Henri Ranaivonjatovo, Heinz Gornitzka, and Jean Escudié. "1,3-Digermacyclobutanes with exocyclic CP and CPS double bonds." Chemical Communications, no. 40 (2007): 4149. http://dx.doi.org/10.1039/b708308d.

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23

Eberl, T. "Di-electron production in C+C and p+p collisions with HADES." European Physical Journal C 49, no. 1 (2006): 261–67. http://dx.doi.org/10.1140/epjc/s10052-006-0097-2.

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24

Tian, Gang, and Dongyi Wei. "Asymptotic of Enumerative Invariants in $${\mathbb {C}}P^2$$ C P 2." Peking Mathematical Journal 1, no. 2 (2018): 125–40. http://dx.doi.org/10.1007/s42543-018-0004-4.

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25

Thomas, Stephen H., and Kenneth A. Williams. "F LIGHT P HYSICIAN T RAINING P ROGRAM —C ORE C ONTENT." Prehospital Emergency Care 6, no. 4 (2002): 458–60. http://dx.doi.org/10.1080/10903120290938148.

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26

Mei, Yanbo, Jaap E. Borger, Dong-Jun Wu, and Hansjörg Grützmacher. "Salen supported Al–O–CP and Ga–PCO complexes." Dalton Transactions 48, no. 13 (2019): 4370–74. http://dx.doi.org/10.1039/c9dt00485h.

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27

Mehta, Yashwant, Vikram V. Dabhade, and Gajanan P. Chaudhari. "Metallography of Fe–P–C and Fe–P–C–Si–N Alloys." Metallography, Microstructure, and Analysis 4, no. 6 (2015): 488–96. http://dx.doi.org/10.1007/s13632-015-0233-1.

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28

Grobe, Joseph, та Duc Le Van. "Reaktive EC (p-p)π-systeme". Journal of Organometallic Chemistry 311, № 1-2 (1986): 37–43. http://dx.doi.org/10.1016/0022-328x(86)80216-9.

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29

Grobe, Joseph, Duc Le Van, Wolfgang Meyring, Bernt Krebs та Mechthild Dartmann. "Reaktive EC (pp)π-Systeme". Journal of Organometallic Chemistry 340, № 2 (1988): 143–51. http://dx.doi.org/10.1016/0022-328x(88)80070-6.

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30

Grobe, Joseph, Duc Le Van та Joachim Welzel. "Reaktive EC (pp) π-Systeme". Journal of Organometallic Chemistry 340, № 2 (1988): 153–60. http://dx.doi.org/10.1016/0022-328x(88)80071-8.

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31

Grobe, Joseph, Duc Le Van, Wolfgang Meyring, Bernt Krebs та Mechtild Dartmann. "Reaktive EC (pp) π-Systeme". Journal of Organometallic Chemistry 346, № 3 (1988): 361–77. http://dx.doi.org/10.1016/0022-328x(88)80137-2.

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32

Grobe, Joseph, Jürgen Szameitat та Manfred Möller. "Reaktive EC (pp) τ-systeme". Journal of Organometallic Chemistry 344, № 1 (1988): 61–69. http://dx.doi.org/10.1016/0022-328x(88)80213-4.

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33

Grobe, Joseph, Duc Le Van, Bernt Krebs та ін. "Reaktive EC (p—p) π-Systeme". Journal of Organometallic Chemistry 399, № 1-2 (1990): 189–98. http://dx.doi.org/10.1016/0022-328x(90)80096-i.

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34

Grobe, Joseph, Marianne Hegemann та Duc Le Van. "Reaktive E=C(p – p)π-Systeme, XX [1] / Reactive E=C(p–p)π-Systems, XX [1]". Zeitschrift für Naturforschung B 45, № 2 (1990): 148–60. http://dx.doi.org/10.1515/znb-1990-0208.

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The vapour phase pyrolysis of the stannylphosphane Me3SnP(CF3)C2F5 (5) at 330 °C leads to 1,2-elimination of Me3SnF yielding a mixture of the two isomeric perfluorophosphaalkenes F3CP=C(F)CF3 (3) and F5C2P=CF2 (4) in a 3:1 molar ratio. 3 is more labile than 4 and proves to be similar to the perfluoro-3-phosphapent-2-ene F5C2P=C(F)CF3 (2) with respect to NMR data and chemical properties. On the other hand 4 resembles the perfluoro-2-phosphapropene F3CP=CF2 (1). These results have been deduced from the following reactivity studies: (i) The rate of dimerization being higher for 3 than for 4. (ii)

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35

Grobe, Joseph, Gudrun Lange та Duc Le Van. "Reaktive E=C(p – p) π-Systeme, XXI [1] / Reactive E=C(p – p)π-Systems, XXI [1]". Zeitschrift für Naturforschung B 45, № 3 (1990): 299–307. http://dx.doi.org/10.1515/znb-1990-0305.

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1λ3,3λ3-Diphosphanes of the type R2PCF2P(H)CF3 [R = Me (3), Et (5), Cyclohexyl (6), Ph (7)] are formed in acceptable yields (40-75%) by reacting perfluoro-2-phosphapropene F3CP=CF2 (1) with the corresponding secondary phosphanes R2PH. By reaction with sulfur, compounds 3, 5 and 7 selectively yield the corresponding monosulfur derivates R2P(S)CF2P(H)CF3 [R = Me (8), Et (9), Ph (10)]. Treatment of 3 or 7 with dimethylamine (molar ratio 1/2) leads via HF elimination and addition of Me2NH to the aminophosphanes R2PCHFP(NMe2)CF3 [R = Me (11), Ph (12)]. In a similar procedure HF has been eliminated

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36

Yang, Chengmin. "Projections P on C = C[ -1, 1 ] which Interpolate at dim(P(C)) or More Points." Proceedings of the American Mathematical Society 115, no. 3 (1992): 669. http://dx.doi.org/10.2307/2159213.

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37

Li, Lili, Wenbin Huang, Lijin Chen, Jiaxing Dong, Xuebing Ma, and Yungui Peng. "Silver-Catalyzed Oxidative C(sp3 )−P Bond Formation through C−C and P−H Bond Cleavage." Angewandte Chemie 129, no. 35 (2017): 10675–80. http://dx.doi.org/10.1002/ange.201704910.

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38

Li, Lili, Wenbin Huang, Lijin Chen, Jiaxing Dong, Xuebing Ma, and Yungui Peng. "Silver-Catalyzed Oxidative C(sp3 )−P Bond Formation through C−C and P−H Bond Cleavage." Angewandte Chemie International Edition 56, no. 35 (2017): 10539–44. http://dx.doi.org/10.1002/anie.201704910.

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39

Turturro, Michael A. "P AIN , P RIORITIES, AND P REHOSPITAL C ARE." Prehospital Emergency Care 6, no. 4 (2002): 486–88. http://dx.doi.org/10.1080/10903120290938238.

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40

Brice, Jane H., Terence Valenzuela, Joseph P. Ornato, et al. "O PTIMAL P REHOSPITAL C ARDIOVASCULAR C ARE." Prehospital Emergency Care 5, no. 1 (2001): 65–72. http://dx.doi.org/10.1080/10903120190940362.

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41

Ziółkowska, Aleksandra, Natalia Szynkiewicz, Jerzy Pikies, and Łukasz Ponikiewski. "Synthesis of compounds with C–P–P and CP–P bond systems based on the phospha-Wittig reaction." Dalton Transactions 49, no. 39 (2020): 13635–46. http://dx.doi.org/10.1039/d0dt02728f.

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This work presents the reactivity of [<sup>Me</sup>NacNacTi(Cl){η<sup>2</sup>-P(SiMe<sub>3</sub>)–PtBu<sub>2</sub>}] towards ketones such as benzophenone, 9-fluorenone, acetophenone, cyclopentanone, cyclohexanone and cycloheptanone based on the phospha-Wittig reaction.

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42

Althoff, Ulrike, Joseph Grobe, Duc Le Van та Ernst-Ulrich Würthwein. "Reaktive E=C(p—p)π-Systenie, XIX. F3CP=C(H)F und F3CP = C(D)F als Dienophile / Reactive E=C(p—p)π-Systems, XIX. F3CP=C(H)F and F3CP=C(D)F as Dienophiles". Zeitschrift für Naturforschung B 44, № 2 (1989): 175–80. http://dx.doi.org/10.1515/znb-1989-0214.

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Abstract A study of the dienophilic properties of F3CP = C(H)F (1) and F3CP = C (D)F (4) has been performed by using Me3SnP(CF3)CF2H (2) and Me3SnP(CF3)CF2D (3), respectively, as precur sors for the in situ generation of 1 and 4 in the presence of 2 ,3-dim ethyl-1,3-butadiene, 1,3-cyclohexadiene or 9,10-dimethylanthracene. Slow elimination of Me3SnF occurs at 55 °C yielding the cycloadducts of 1 and 4, respectively, within 5 or 7 days. Polymerization is observed as the main stabilizing reaction of 1 and 4, thus reducing the yields o f the [2+4]-cycloadducts 5 to 9 to about 20%. They are forme

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43

Oglesbee, Michael. "Cellular Responses to Stress. C. P. Downes , C. R. Wolf , D. P. Lane." Quarterly Review of Biology 75, no. 4 (2000): 454. http://dx.doi.org/10.1086/393653.

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44

Ishikawa, H., R. W. Field, S. C. Farantos, et al. "ChemInform Abstract: H-CP-CP-H Isomerization: Caught in the Act." ChemInform 31, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.200017287.

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45

Antonelli, A., P. Fallahi, S. M. Ferrari, et al. "High Circulating Chemokines (C-X-C Motif) Ligand 9, and (C-X-C Motif) Ligand 11, in Hepatitis C-Associated Cryoglobulinemia." International Journal of Immunopathology and Pharmacology 26, no. 1 (2013): 49–57. http://dx.doi.org/10.1177/039463201302600105.

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(C-X-C motif) ligand 9 and (C-X-C motif) ligand 11 (CXCL9 and CXCL11), are potent chemoattractants for activated T cells, and play an important role in T helper 1 (Th) 1 cell recruitment in chronic hepatitis C. No study has evaluated CXCL9, together with CXCL11, circulating levels in patients with mixed cryoglobulinemia and hepatitis C (MC+HCV-p). The aim of the present study therefore was to measure serum CXCL9, and CXCL11 levels, in MC+HCV-p, and to relate the findings to the clinical phenotype. Serum CXCL9 and CXCL11 were measured in 71 MC+HCV-p and in matched controls. MC+HCV-p showed sign

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46

M�ller, H. "Deuteron fragmentationd+p?p+p+n at 9 GeV/c." Zeitschrift f�r Physik A Atomic Nuclei 332, no. 3 (1989): 361–62. http://dx.doi.org/10.1007/bf01295467.

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47

Crossley, M. D. "Monomial Bases for $H^*(\mathbf {C}P^\infty \times \mathbf {C}P^\infty )$ over $\mathcal A(p)$." Transactions of the American Mathematical Society 351, no. 1 (1999): 171–92. http://dx.doi.org/10.1090/s0002-9947-99-02060-7.

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48

Paju, Martti, Helmut Viefhaus, and Hans Jürgen Grabke. "Phosphorus segregation in austenite in Fe-P-C, Fe-P-B and Fe-P-C-B alloys." Steel Research 59, no. 8 (1988): 336–43. http://dx.doi.org/10.1002/srin.198801524.

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49

García, M. Esther, Daniel García-Vivó, Miguel A. Ruiz, and David Sáez. "Divergent Reactivity of a Phosphinidene-Bridged Dimolybdenum Complex Toward 1-Alkynes: P–C, P–H, C–C, and C–H Couplings." Organometallics 36, no. 9 (2017): 1756–64. http://dx.doi.org/10.1021/acs.organomet.7b00121.

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50

Zhu, Zhanmin. "C-coherent rings, C-semihereditary rings and C-regular rings." Studia Scientiarum Mathematicarum Hungarica 50, no. 4 (2013): 491–508. http://dx.doi.org/10.1556/sscmath.50.2013.4.1256.

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Abstract:

Let C be a class of some finitely presented left R-modules. A left R-module M is called C-injective, if ExtR1(C, M) = 0 for each C ∈ C. A right R-module M is called C-flat, if Tor1R(M, C) = 0 for each C ∈ C. A ring R is called C-coherent, if every C ∈ C is 2-presented. A ring R is called C-semihereditary, if whenever 0 → K → P → C → 0 is exact, where C ∈ C and P is finitely generated projective and K is finitely generated, then K is also projective. A ring R is called C-regular, if whenever P/K ∈ C, where P is finitely generated projective and K is finitely generated, then K is a direct summan

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