Relevant bibliographies by topics / Hydrophosphonylation

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Hydrophosphonylation'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 April 2022

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Journal articles on the topic "Hydrophosphonylation"

1

Alegre-Requena, Juan V., Eugenia Marqués-López, Pablo J. Sanz Miguel, and Raquel P. Herrera. "Organocatalytic enantioselective hydrophosphonylation of aldehydes." Org. Biomol. Chem. 12, no. 8 (2014): 1258–64. http://dx.doi.org/10.1039/c3ob42403k.

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Rulev, A. Yu. "Hydrophosphonylation of α-Haloalkenals". Heteroatom Chemistry 24, № 3 (2013): 187–90. http://dx.doi.org/10.1002/hc.21081.

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Ooi, T., D. Uraguchi, T. Ito, and S. Nakamura. "Asymmetric Hydrophosphonylation of Ynones." Synfacts 2011, no. 01 (2010): 0050. http://dx.doi.org/10.1055/s-0030-1259171.

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Zeng, Youmao, Ping Deng, Shixiong Zhang, et al. "An Ni–PyBisulidine complex for the asymmetric hydrophosphonylation of aldehydes." Organic & Biomolecular Chemistry 14, no. 39 (2016): 9221–24. http://dx.doi.org/10.1039/c6ob01750a.

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Liu, Yizhen, Xiaoting Fan, Zhen Hua Li, and Huadong Wang. "Activation of the P–H bond by a frustrated Lewis pair and its application in catalytic Z-selective hydrophosphonylation of terminal ynones." Chemical Communications 53, no. 79 (2017): 10890–93. http://dx.doi.org/10.1039/c7cc05028c.

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Geant, Pierre-Yves, Bemba Sidi Mohamed, Christian Périgaud, Suzanne Peyrottes, Jean-Pierre Uttaro, and Christophe Mathé. "Probing the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under free-radical conditions." New Journal of Chemistry 40, no. 6 (2016): 5318–24. http://dx.doi.org/10.1039/c6nj00123h.

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Deng, Tao, and Chun Cai. "Bis(oxazoline)-copper catalyzed enantioselective hydrophosphonylation of aldehydes." RSC Adv. 4, no. 53 (2014): 27853–56. http://dx.doi.org/10.1039/c4ra03269a.

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Mao, Liu-Liang, Chen-Chen Li, Qiang Yang, Ming-Xing Cheng та Shang-Dong Yang. "One-pot synthesis of α-aminophosphonates via a cascade sequence of allylamine isomerization/hydrophosphonylation". Chemical Communications 53, № 32 (2017): 4473–76. http://dx.doi.org/10.1039/c7cc01391d.

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Sidi Mohamed, Bemba, Christian Périgaud, Suzanne Peyrottes, Jean-Pierre Uttaro, and Christophe Mathé. "Rapid synthesis of carbonucleoside phophonate analogues as potential antiviral agents via a hydrophosphonylation reaction of ethynyl carbocyclic precursors." New Journal of Chemistry 42, no. 2 (2018): 974–79. http://dx.doi.org/10.1039/c7nj03991c.

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Wang, Lisheng, Fuxing Yang, Xiaoping Xu, and Jun Jiang. "Organocatalytic 1,6-hydrophosphination of para-quinone methides: enantioselective access to chiral 3-phosphoxindoles bearing phosphorus-substituted quaternary carbon stereocenters." Organic Chemistry Frontiers 8, no. 9 (2021): 2002–8. http://dx.doi.org/10.1039/d0qo01638a.

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Dissertations / Theses on the topic "Hydrophosphonylation"

1

Ould, Sidi Mohamed Bemba. "Synthèse de carbonucléosides phosphonates à visée antivirale." Thesis, Montpellier, 2016. http://www.theses.fr/2016MONTT234/document.

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Les analogues de nucléosides ont été largement utilisés dans le traitement d’affections d’origine virale grâce à l’activité biologique de ces dérivés. Nous nous sommes particulièrement intéressés dans ce travail à l’étude de carbonucléosides phosphonates. Le premier chapitre de cette thèse rapporte une étude bibliographique sur les virus et les analogues nucléosidiques approuvés par la FDA. Les mécanismes d’action de ces analogues ont été également abordés dans ce chapitre. Dans le deuxième chapitre, nous avons décrit la synthèse des dérivés 2’- ou 4’-hydroxy-4’-carbonucléoside méthyle phospho
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Mkwakwi, Kwakhanya. "Synthesis and characterisation of lanthanide complexes with O,O-donor ligands: towards a new generation of hydrophosphonylation catalysts." Thesis, Nelson Mandela Metropolitan University, 2017. http://hdl.handle.net/10948/11986.

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This study investigates the coordination behaviour of potentially bi- and tridentate O,O- and O,N,O-donor Schiff base ligands with trivalent lanthanide ions. The reactions of lanthanide nitrates with 2-((E)-(tert-butylimino)methyl)-6-methoxyphenol (HL1) have yielded five complexes that are described by the general formula [Ln(HL1)2(NO3)3] (Ln = Ce, Nd, Gd, Ho and Er) and were characterised using physico-chemical techniques including single-crystal X-ray diffraction spectroscopy. The cerium complex crystallised in a triclinic (P-1) space group, while the rest of the complexes crystallised in th
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Chassillan, Louis. "New Chiral Bifunctional Organocatalysts : Synthesis and Application in Enantioselective Reactions Under Batch and Continuous-Flow Conditions." Thesis, université Paris-Saclay, 2022. http://www.theses.fr/2022UPASF027.

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Au cours des dernières années, l’organocatalyse asymétrique a connu un engouement sans précédent et de nombreux catalyseurs organiques ont été synthétisés dans le but d’effectuer des réactions plus rapides et plus sélectives. Cependant, étant donné la demande croissante de molécules chirales dans l’industrie, il demeure crucial de développer de nouveaux outils afin de rendre leur production plus efficace. Pour ce faire, l’utilisation de la catalyse bifonctionnelle apparait comme une évidence du fait de sa capacité à activer simultanément le nucléophile et l’électrophile et ainsi permettre un m
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Book chapters on the topic "Hydrophosphonylation"

1

Hof, K., K. M. Lippert, and P. R. Schreiner. "Hydrophosphonylation." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00262.

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Uraguchi, D., and T. Ooi. "Hydrophosphonylation Reactions." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00317.

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Hof, K., K. M. Lippert, and P. R. Schreiner. "Hydrophosphonylation of Imines." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00263.

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Reznichenko, A. L., and K. C. Hultzsch. "Hydrophosphinylation, Hydrophosphonylation, and Hydrophosphination." In Stereoselective Synthesis 1 Stereoselective Reactions of Carbon—Carbon Double Bonds. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-201-00390.

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Reznichenko, A. L., and K. C. Hultzsch. "Hydrophosphonylation of Styrene and Norbornene." In Stereoselective Synthesis 1 Stereoselective Reactions of Carbon—Carbon Double Bonds. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-201-00392.

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Hof, K., K. M. Lippert, and P. R. Schreiner. "Hydrophosphonylation of α-Keto Esters." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00264.

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Bergin, E. "Hydrophosphonylation of Carbonyl and Imino Groups." In Stereoselective Reactions of Carbonyl and Imino Groups. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-202-00296.

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Singh, R. P., and L. Deng. "Hydrophosphonylation Reaction of Imines with Phosphites." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00081.

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"Hydrocyanation, Cyanosilylation, and Hydrophosphonylation of Carbonyl and Imino Groups." In Stereoselective Synthesis 2, edited by G. A. Molander. Georg Thieme Verlag, 2011. http://dx.doi.org/10.1055/sos-sd-202-00528.

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"Hydrocyanation, Cyanosilylation, and Hydrophosphonylation of Carbonyl and Imino Groups." In Stereoselective Synthesis 2, edited by G. A. Molander. Georg Thieme Verlag, 2011. http://dx.doi.org/10.1055/sos-sd-202-00528.

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