Einloggen

Thematische Bibliographien / P-Stereogenic catalysts / Zeitschriftenartikel

Zeitschriftenartikel zum Thema „P-Stereogenic catalysts“

Um die anderen Arten von Veröffentlichungen zu diesem Thema anzuzeigen, folgen Sie diesem Link: P-Stereogenic catalysts.

Autor: Grafiati

Veröffentlicht am 25. Mai 2024

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit Top-50 Zeitschriftenartikel für die Forschung zum Thema "P-Stereogenic catalysts" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Sehen Sie die Zeitschriftenartikel für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.

1

Błaszczyk, Jarosław, Bogdan Bujnicki, Patrycja Pokora-Sobczak, Grażyna Mielniczak, Lesław Sieroń, Piotr Kiełbasiński und Józef Drabowicz. „New Optically Active tert-Butylarylthiophosphinic Acids and Their Selenium Analogues as the Potential Synthons of Supramolecular Organometallic Complexes: Syntheses and Crystallographic Structure Determination“. Molecules 28, Nr. 11 (24.05.2023): 4298. http://dx.doi.org/10.3390/molecules28114298.

Der volle Inhalt der Quelle

Annotation:

The aim of the research described in this publication is two-fold. The first is a detailed description of the synthesis of a series of compounds containing a stereogenic heteroatom, namely the optically active P-stereogenic derivatives of tert-butylarylphoshinic acids bearing sulfur or selenium. The second is a detailed discussion dedicated to the determination of their structures by an X-ray analysis. Such a determination is needed when considering optically active hetero-oxophosphoric acids as new chiral solvating agents, precursors of new chiral ionic liquids, or ligands in complexes serving as novel organometallic catalysts.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

Han, Zhengxu S., Hao Wu, Bo Qu, Yuwen Wang, Ling Wu, Li Zhang, Yibo Xu et al. „New class of P-stereogenic chiral Brønsted acid catalysts derived from chiral phosphinamides“. Tetrahedron Letters 60, Nr. 28 (Juli 2019): 1834–37. http://dx.doi.org/10.1016/j.tetlet.2019.06.013.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

von Münchow, Tristan, Suman Dana, Yang Xu, Binbin Yuan und Lutz Ackermann. „Enantioselective electrochemical cobalt-catalyzed aryl C–H activation reactions“. Science 379, Nr. 6636 (10.03.2023): 1036–42. http://dx.doi.org/10.1126/science.adg2866.

Der volle Inhalt der Quelle

Annotation:

Enantioselective redox transformations typically rely on costly transition metals as catalysts and often stoichiometric amounts of chemical redox agents as well. Electrocatalysis represents a more sustainable alternative, in particular through the use of the hydrogen evolution reaction (HER) in place of a chemical oxidant. In this work, we describe strategies for HER-coupled enantioselective aryl carbon-hydrogen bond (C–H) activation reactions using cobalt in place of a precious metal catalyst for the asymmetric oxidation. Thus, highly enantioselective carbon-hydrogen and nitrogen-hydrogen (C–H and N–H) annulations of carboxylic amides were achieved, which gave access to point and axially chiral compounds. Furthermore, the cobalt-mediated electrocatalysis enabled the preparation of various phosphorus (P)–stereogenic compounds by selective desymmetrization through dehydrogenative C–H activation reactions.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

Chan, Vincent S., Melanie Chiu, Robert G. Bergman und F. Dean Toste. „Development of Ruthenium Catalysts for the Enantioselective Synthesis of P-Stereogenic Phosphines via Nucleophilic Phosphido Intermediates“. Journal of the American Chemical Society 131, Nr. 16 (29.04.2009): 6021–32. http://dx.doi.org/10.1021/ja9014887.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

Gladiali, Serafino, Serenella Medici, Giovanna Pirri, Sonia Pulacchini und Davide Fabbri. „BINAPS - An axially chiral P,S-heterodonor ligand for asymmetric catalysis based on binaphthalene backbone“. Canadian Journal of Chemistry 79, Nr. 5-6 (01.05.2001): 670–78. http://dx.doi.org/10.1139/v01-041.

Der volle Inhalt der Quelle

Annotation:

The chelating P,S-heterodonor ligand 2-diphenylphosphanyl-1,1'-binaphthalene-2'-thiol (11) (BINAPS), which features a chiral axis as the unique stereogenic element, has been prepared in both racemic and enantiopure form through a multistep reaction sequence using 2,2'-dihydroxy-1,1'-binaphthalene (BINOL) as the starting material. The reaction sequence is completely stereoconservative and (S)-11 is obtained with no loss of enantiopurity from pure (S)-BINOL. (R)-11 can be alternatively obtained by resolution of racemic 11 using the chiral (S)-benzylaminato Pd(II)-complex 19 as the resolving agent. The S-methyl or the S-i-propyl derivatives 14 have been used as chiral ligands in the Rh(I)-catalyzed asymmetric hydroformylation of styrene and in the hydrogen transfer reduction of acetophenone with modest success (up to 20% ee). In the presence of suitable Pd-complexes the same ligands provide higher ees in the hydrosilylation of styrene (50% ee) and in the allylic alkylation of 1,3-diphenylprop-2-enyl acetate (60% ee).Key words: heterodonor ligands, binaphthalene derivatives, enantioselective catalysis, transition metal catalysts, allylic alkylation.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

Biosca, Maria, Ernest Salomó, Pol de la Cruz-Sánchez, Antoni Riera, Xavier Verdaguer, Oscar Pàmies und Montserrat Diéguez. „Extending the Substrate Scope in the Hydrogenation of Unfunctionalized Tetrasubstituted Olefins with Ir-P Stereogenic Aminophosphine–Oxazoline Catalysts“. Organic Letters 21, Nr. 3 (16.01.2019): 807–11. http://dx.doi.org/10.1021/acs.orglett.8b04084.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

Bagi, Péter, Réka Herbay, Gábor Györke, Péter Pongrácz, László Kollár, István Timári, László Drahos und György Keglevich. „Preparation of Palladium(II) Complexes of 1-substituted-3-phospholene Ligands and their Evaluation as Catalysts in Hydroalkoxycarbonylation“. Current Organic Chemistry 23, Nr. 25 (14.01.2020): 2873–79. http://dx.doi.org/10.2174/1385272823666191204151311.

Der volle Inhalt der Quelle

Annotation:

: A series of palladium(II) complexes incorporating 1-substituted-3-methyl-3- phospholenes as the P-ligands were prepared from phospholene oxides by deoxygenation followed by complexation with PdCl2(PhCN)2. The two 1-substituted-3-methyl-3- phospholene ligands were trans position to each other in the Pd(II)-complexes. As the ligands contain a P-stereogenic center, the Pd-complexes were obtained as a 1:1 mixture of two stereoisomers, the homochiral (R,R and S,S) and the meso (R,S) forms, when racemic starting materials were used. An optically active Pd-complex containing (R)-1-propyl- 3-phospholene ligand was also prepared. Catalytic activity of an aryl- and an alkyl-3- phospholene-palladium(II)-complex was evaluated in hydroalkoxycarbonylation of styrene. The alkyl-derivative showed higher activity and selectivity towards the formation of the esters of 3-phenylpropionic acid. However, the overall activity of these PdCl2(phospholene)2-type complexes was low.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

8

Huber, Raffael, Alessandro Passera, Erik Gubler und Antonio Mezzetti. „P-Stereogenic PN(H)P Iron(II) Catalysts for the Asymmetric Hydrogenation of Ketones: The Importance of Non-Covalent Interactions in Rational Ligand Design by Computation“. Advanced Synthesis & Catalysis 360, Nr. 15 (22.06.2018): 2900–2913. http://dx.doi.org/10.1002/adsc.201800433.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

9

Numan, Ahmed, und Matthew Brichacek. „Asymmetric Synthesis of Stereogenic Phosphorus P(V) Centers Using Chiral Nucleophilic Catalysis“. Molecules 26, Nr. 12 (15.06.2021): 3661. http://dx.doi.org/10.3390/molecules26123661.

Der volle Inhalt der Quelle

Annotation:

Organophosphates have been widely used in agrochemistry, as reagents for organic synthesis, and in biochemistry. Phosphate mimics possessing four unique substituents, and thereby a chirality center, are useful in transition metal catalysis and as nucleotide therapeutics. The catalytic, stereocontrolled synthesis of phosphorus-stereogenic centers is challenging and traditionally depends on a resolution or use of stochiometric auxiliaries. Herein, enantioenriched phosphorus centers have been synthesized using chiral nucleophilic catalysis. Racemic H-phosphinate species were coupled with nucleophilic alcohols under halogenating conditions. Chiral phosphonate products were synthesized in acceptable yields (33–95%) and modest enantioselectivity (up to 62% ee) was observed after identification of an appropriate chiral catalyst and optimization of the solvent, base, and temperature. Nucleophilic catalysis has a tremendous potential to produce enantioenriched phosphate mimics that could be used as prodrugs or chemical biology probes.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

10

Funk, Michael A. „A P catalyst for stereogenic P(III)“. Science 371, Nr. 6530 (11.02.2021): 687.5–687. http://dx.doi.org/10.1126/science.371.6530.687-e.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

11

Xiang, Yijun, Qianyi Ge, Shulei Wu, Xing Zheng und Zehua Yang. „Synthesis and application in asymmetric catalysis of P-stereogenic pincer–metal complexes“. RSC Advances 10, Nr. 16 (2020): 9563–78. http://dx.doi.org/10.1039/d0ra00377h.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

12

Xie, Xiaoxiao, Sanliang Li, Qiaoyu Chen, Hao Guo, Junfeng Yang und Junliang Zhang. „Synthesis and application of novel P-chiral monophosphorus ligands“. Organic Chemistry Frontiers 9, Nr. 6 (2022): 1589–92. http://dx.doi.org/10.1039/d1qo01819a.

Der volle Inhalt der Quelle

Annotation:

A series of novel P-stereogenic monophosphorus ligands (Xie-phos) were synthesized via the hydrophosphinylation of alkynes with secondary phosphine oxides by palladium catalysis and the following base mediated cyclization.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

13

Schwenk, R., und A. Togni. „P-Trifluoromethyl ligands derived from Josiphos in the Ir-catalysed hydrogenation of 3,4-dihydroisoquinoline hydrochlorides“. Dalton Transactions 44, Nr. 45 (2015): 19566–75. http://dx.doi.org/10.1039/c5dt02019k.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

14

Rojo, Pep, Antoni Riera und Xavier Verdaguer. „Bulky P-stereogenic ligands. A success story in asymmetric catalysis“. Coordination Chemistry Reviews 489 (August 2023): 215192. http://dx.doi.org/10.1016/j.ccr.2023.215192.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

15

Nagel, Ulrich, und Christoph Roller. „Enantioselektive Katalyse, XVIII Der Einfluß nicht koordinierter Stereozentren auf die enantioselektive Hydrierung/Enantioselective Catalysis, XVIII The Influence of Non-Coordinated Stereocenters on the Enantioselective Hydrogenation“. Zeitschrift für Naturforschung B 53, Nr. 2 (01.02.1998): 211–23. http://dx.doi.org/10.1515/znb-1998-0213.

Der volle Inhalt der Quelle

Annotation:

Abstract 3,4-Bis{[2-(methyl-phenyl-oxophosphanyl)-ethyl]phenyl-phosphanyl}pyrrolidines have been synthesized by Michael Addition from the corresponding methyl-phenyl-vinyl-phosphane oxides and 3,4-bis(phenylphosphino)pyrrolidines. For purification of the ligands palladium complexes were used and with the enantiomerically pure ligands Rh complexes have been prepared. The catalyst has 6 stereogenic centers. In the hydrogenation of Z-α-acetamidocinnamic acid all six stereogenic centers have an influence on the enantioselectivity. The influence is strongest from the C stereocenters of the pyrrolidine ring. Less important are the stereogenic centers on the coordinated P atoms. The influence of the stereocenters on the non-coordinated P = O groups is the least, but it is not negligible. The ee values obtained with the ligands containing P = O groups are much lower than those obtained with ligands which are substituted only with aryl groups. Ketones are hydrogenated with only low ee’s.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

16

Grabulosa, Arnald, Alberto Mannu, Guillermo Muller, Teresa Calvet und Mercè Font-Bardia. „P-Stereogenic monophosphines in Pd-catalysed enantioselective hydrovinylation of styrene“. Journal of Organometallic Chemistry 696, Nr. 11-12 (Juni 2011): 2338–45. http://dx.doi.org/10.1016/j.jorganchem.2011.02.034.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

17

Ramazanova, Kyzgaldak, Soumyadeep Chakrabortty, Bernd H. Müller, Peter Lönnecke, Johannes G. de Vries und Evamarie Hey-Hawkins. „Synthesis of P-stereogenic 1-phosphanorbornane-derived phosphine–phosphite ligands and application in asymmetric catalysis“. RSC Advances 13, Nr. 49 (2023): 34439–44. http://dx.doi.org/10.1039/d3ra07630j.

Der volle Inhalt der Quelle

Annotation:

A convenient synthesis of enantiopure mixed donor phosphine–phosphite ligands has been developed incorporating P-stereogenic phosphanorbornane and axially chiral bisnaphthols into one ligand structure.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

18

Álvarez-Yebra, Rubén, Pep Rojo, Antoni Riera und Xavier Verdaguer. „Iridium complexes with P-stereogenic phosphino imidazole ligands: Synthesis, structure and catalysis“. Tetrahedron 75, Nr. 32 (August 2019): 4358–64. http://dx.doi.org/10.1016/j.tet.2019.04.032.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

19

Zhang, Jieming, Hang Ni, Qi Wu, Junfeng Yang und Junliang Zhang. „Development of P, S and Si-Stereogenic Compounds Synthesis via Palladium Catalysis“. Chinese Journal of Organic Chemistry 42, Nr. 10 (2022): 3118. http://dx.doi.org/10.6023/cjoc202208043.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

20

Sondenecker, Aline, Ján Cvengroš, Raphael Aardoom und Antonio Togni. „P-Stereogenic Ferrocene-Based (Trifluoromethyl)phosphanes: Synthesis, Structure, Coordination Properties and Catalysis“. European Journal of Organic Chemistry 2011, Nr. 1 (12.11.2010): 78–87. http://dx.doi.org/10.1002/ejoc.201001162.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

21

Han, Zhengxu S., Li Zhang, Yibo Xu, Joshua D. Sieber, Maurice A. Marsini, Zhibin Li, Jonathan T. Reeves et al. „Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design“. Angewandte Chemie International Edition 54, Nr. 18 (10.03.2015): 5474–77. http://dx.doi.org/10.1002/anie.201500350.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

22

Han, Zhengxu S., Li Zhang, Yibo Xu, Joshua D. Sieber, Maurice A. Marsini, Zhibin Li, Jonathan T. Reeves et al. „Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design“. Angewandte Chemie 127, Nr. 18 (10.03.2015): 5564–67. http://dx.doi.org/10.1002/ange.201500350.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

23

Berger, Olivier, und Jean-Luc Montchamp. „A General Strategy for the Synthesis of P-Stereogenic Compounds“. Angewandte Chemie International Edition 52, Nr. 43 (09.09.2013): 11377–80. http://dx.doi.org/10.1002/anie.201306628.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

24

Balkaner, Orçun, Derya Işıl Sarıoğulları und Aylin Uslu. „A synthetic strategy of P-stereogenic ligands for catalysis: Examples based on cyclotriphosphazenes“. Journal of Molecular Structure 1261 (August 2022): 132834. http://dx.doi.org/10.1016/j.molstruc.2022.132834.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

25

Cabré, Albert, Antoni Riera und Xavier Verdaguer. „P-Stereogenic Amino-Phosphines as Chiral Ligands: From Privileged Intermediates to Asymmetric Catalysis“. Accounts of Chemical Research 53, Nr. 3 (27.02.2020): 676–89. http://dx.doi.org/10.1021/acs.accounts.9b00633.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

26

Harvey, James Stephen, und Véronique Gouverneur. „Catalytic enantioselective synthesis of P-stereogenic compounds“. Chemical Communications 46, Nr. 40 (2010): 7477. http://dx.doi.org/10.1039/c0cc01939a.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

27

Dziuba, Kamil, Małgorzata Lubańska und K. Michał Pietrusiewicz. „Enantiodivergent Synthesis of Both PAMPO Enantiomers Using l-Menthyl Chloroacetate and Stereomutation at P in Classical Quaternisation Reactions“. Synthesis 52, Nr. 06 (04.12.2019): 909–16. http://dx.doi.org/10.1055/s-0039-1691531.

Der volle Inhalt der Quelle

Annotation:

A practical protocol for efficient synthesis of both PAMPO enantiomers as well as related functionalised P-stereogenic phosphine oxides in 1–3 steps from effectively resolved (S P)-l-menthyl o-anisyl-(phenyl)phosphinylacetate has been developed. Examples of non-stereoselective quaternisation of a tertiary phosphine by alkyl halides have been revealed.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

28

Vinokurov, Nikolai, K. Michał Pietrusiewicz, Sławomir Frynas, Michael Wiebcke und Holger Butenschön. „Asymmetric 1,3-dipolar cycloaddition with a P-stereogenic dipolarophile: An efficient approach to novel P-stereogenic 1,2-diphosphine systems“. Chemical Communications, Nr. 42 (2008): 5408. http://dx.doi.org/10.1039/b810573a.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

29

Whittaker, Benjamin, Manuel de Lera Ruiz und Christopher J. Hayes. „Stereoselective synthesis of highly functionalised P-stereogenic nucleosides via palladium-catalysed P–C cross-coupling reactions“. Tetrahedron Letters 49, Nr. 49 (Dezember 2008): 6984–87. http://dx.doi.org/10.1016/j.tetlet.2008.09.102.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

30

Buergler, Jonas F., Katrin Niedermann und Antonio Togni. „P-Stereogenic Trifluoromethyl Derivatives of Josiphos: Synthesis, Coordination Properties, and Applications in Asymmetric Catalysis“. Chemistry - A European Journal 18, Nr. 2 (08.12.2011): 632–40. http://dx.doi.org/10.1002/chem.201102390.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

31

Schmitz, Christian, Walter Leitner und Giancarlo Franciò. „Synthesis of P-Stereogenic Phosphoramidite and Phosphorodiamidite Ligands and Their Application in Asymmetric Catalysis“. European Journal of Organic Chemistry 2015, Nr. 28 (12.08.2015): 6205–30. http://dx.doi.org/10.1002/ejoc.201500767.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

32

Han, Zhengxu S., und et al. „ChemInform Abstract: Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design.“ ChemInform 46, Nr. 36 (20.08.2015): no. http://dx.doi.org/10.1002/chin.201536217.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

33

Mutlu, Ömer Faruk, Arzu Binici, Aytuğ Okumuş, Gamze Elmas, Bünyemin Çoşut, Zeynel Kılıç und Tuncer Hökelek. „Phosphorus–nitrogen compounds. Part 54. syntheses of chiral amino-4-fluorobenzyl-spiro(N/O)cyclotriphosphazenes: structural and stereogenic properties“. New Journal of Chemistry 45, Nr. 27 (2021): 12178–92. http://dx.doi.org/10.1039/d1nj00934f.

Der volle Inhalt der Quelle

Annotation:

Syntheses, spectral and crystallographic characterizations and stereogenic properties by ³¹P NMR spectra recorded with the addition of CSA, CD spectra and chiral HPLC of amino-4-fluorobenzylspiro(N/O)cyclotriphosphazenes were examined.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

34

Imoto, Hiroaki, Yasuhiro Morisaki und Yoshiki Chujo. „Synthesis and coordination behaviors of P-stereogenic polymers“. Chemical Communications 46, Nr. 40 (2010): 7542. http://dx.doi.org/10.1039/c0cc03120h.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

35

Dorta, Romano, Alberto Herrera, Anthony Linden, Frank Heinemann, René-Chris Brachvogel und Max von Delius. „Optimized Syntheses of Optically Pure P-Alkene Ligands: Crystal Structures of a Pair of P-Stereogenic Diastereomers“. Synthesis 48, Nr. 08 (17.02.2016): 1117–21. http://dx.doi.org/10.1055/s-0035-1560410.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

36

Join, Benoît, David Mimeau, Olivier Delacroix und Annie-Claude Gaumont. „Pallado-catalysed hydrophosphination of alkynes: access to enantio-enriched P-stereogenic vinyl phosphine–boranes“. Chem. Commun., Nr. 30 (2006): 3249–51. http://dx.doi.org/10.1039/b607434k.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

37

Christ, M. Lorraine, Maria Zablocka, Sally Spencer, Rebecca J. Lavender, Marc Lemaire und Jean Pierre Majoral. „Cyclic β-iminophosphine: New P-stereogenic ligand for the asymmetric catalysed hydrogenation of ketones“. Journal of Molecular Catalysis A: Chemical 245, Nr. 1-2 (Februar 2006): 210–16. http://dx.doi.org/10.1016/j.molcata.2005.09.043.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

38

Clavero, Pau, Arnald Grabulosa, Mercè Font-Bardia und Guillermo Muller. „P-Stereogenic monophosphines with the 2-p-terphenylyl and 1-pyrenyl substituents. Application to Pd and Ru asymmetric catalysis“. Journal of Molecular Catalysis A: Chemical 391 (September 2014): 183–90. http://dx.doi.org/10.1016/j.molcata.2014.04.026.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

39

Schmitz, Christian, Walter Leitner und Giancarlo Francio. „ChemInform Abstract: Synthesis of P-Stereogenic Phosphoramidite and Phosphorodiamidite Ligands and Their Application in Asymmetric Catalysis.“ ChemInform 47, Nr. 7 (Januar 2016): no. http://dx.doi.org/10.1002/chin.201607021.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

40

Clarke, Eoin F., Eoin Rafter, Helge Müller-Bunz, Lee J. Higham und Declan G. Gilheany. „The synthesis of P-stereogenic MOP analogues and their use in rhodium catalysed asymmetric addition“. Journal of Organometallic Chemistry 696, Nr. 23 (November 2011): 3608–15. http://dx.doi.org/10.1016/j.jorganchem.2011.08.010.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

41

Nishida, Goushi, Keiichi Noguchi, Masao Hirano und Ken Tanaka. „Enantioselective Synthesis of P-Stereogenic Alkynylphosphine Oxides by Rh-Catalyzed [2+2+2] Cycloaddition“. Angewandte Chemie International Edition 47, Nr. 18 (21.04.2008): 3410–13. http://dx.doi.org/10.1002/anie.200800144.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

42

Vinokurov, Nikolai, K. Michal Pietrusiewicz und Holger Butenschön. „Asymmetric Diels–Alder cycloaddition of a di-P-stereogenic dienophile with cyclopentadiene“. Tetrahedron: Asymmetry 20, Nr. 9 (Mai 2009): 1081–85. http://dx.doi.org/10.1016/j.tetasy.2009.03.022.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

43

Reichl, Kyle D., Daniel H. Ess und Alexander T. Radosevich. „Catalyzing Pyramidal Inversion: Configurational Lability of P-Stereogenic Phosphines via Single Electron Oxidation“. Journal of the American Chemical Society 135, Nr. 25 (17.06.2013): 9354–57. http://dx.doi.org/10.1021/ja404943x.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

44

Bergin, Enda, Cormac T. O'Connor, Shane B. Robinson, Eoghan M. McGarrigle, Colm P. O'Mahony und Declan G. Gilheany. „Synthesis of P-Stereogenic Phosphorus Compounds. Asymmetric Oxidation of Phosphines under Appel Conditions“. Journal of the American Chemical Society 129, Nr. 31 (August 2007): 9566–67. http://dx.doi.org/10.1021/ja072925l.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

45

Huang, Zhijian, Xuan Huang, Baosheng Li, Chengli Mou, Song Yang, Bao-An Song und Yonggui Robin Chi. „Access to P-Stereogenic Phosphinates via N-Heterocyclic Carbene-Catalyzed Desymmetrization of Bisphenols“. Journal of the American Chemical Society 138, Nr. 24 (10.06.2016): 7524–27. http://dx.doi.org/10.1021/jacs.6b04624.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

46

Scriban, Corina, und David S. Glueck. „Platinum-Catalyzed Asymmetric Alkylation of Secondary Phosphines: Enantioselective Synthesis of P-Stereogenic Phosphines“. Journal of the American Chemical Society 128, Nr. 9 (März 2006): 2788–89. http://dx.doi.org/10.1021/ja058096q.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

47

Harvey, James Stephen, Steven J Malcolmson, Katherine S Dunne, Simon J Meek, Amber L Thompson, Richard R Schrock, Amir H Hoveyda und Véronique Gouverneur. „Enantioselective Synthesis of P-Stereogenic Phosphinates and Phosphine Oxides by Molybdenum-Catalyzed Asymmetric Ring-Closing Metathesis“. Angewandte Chemie International Edition 48, Nr. 4 (12.01.2009): 762–66. http://dx.doi.org/10.1002/anie.200805066.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

48

Granander, Johan, Francesco Secci, Peter O’Brien und Brian Kelly. „Kinetic resolution of P-stereogenic phosphine boranes via deprotonation using s-butyllithium/(−)-sparteine“. Tetrahedron: Asymmetry 20, Nr. 21 (November 2009): 2432–34. http://dx.doi.org/10.1016/j.tetasy.2009.10.026.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

49

Moulin, Dominique, Sébastien Bago, Christophe Bauduin, Christophe Darcel und Sylvain Jugé. „Asymmetric synthesis of P-stereogenic o-hydroxyaryl-phosphine (borane) and phosphine-phosphinite ligands“. Tetrahedron: Asymmetry 11, Nr. 19 (Oktober 2000): 3939–56. http://dx.doi.org/10.1016/s0957-4166(00)00372-4.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

50

Williams, B. Scott, Paulo Dani, Martin Lutz, Anthony L Spek und Gerard van Koten. „Development of the First P-Stereogenic PCP Pincer Ligands, Their Metallation by Palladium and Platinum, and Preliminary Catalysis“. Helvetica Chimica Acta 84, Nr. 11 (14.11.2001): 3519–30. http://dx.doi.org/10.1002/1522-2675(20011114)84:11<3519::aid-hlca3519>3.0.co;2-9.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!