Auswahl der wissenschaftlichen Literatur zum Thema „Azetines“
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Zeitschriftenartikel zum Thema "Azetines"
Baumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw und Dorian Didier. „Methods for the Synthesis of Substituted Azetines“. Organic Letters 19, Nr. 20 (04.10.2017): 5681–84. http://dx.doi.org/10.1021/acs.orglett.7b02847.
Der volle Inhalt der QuelleHodgson, David M., Christopher I. Pearson und Madiha Kazmi. „Generation and Electrophile Trapping of N-Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines“. Organic Letters 16, Nr. 3 (10.01.2014): 856–59. http://dx.doi.org/10.1021/ol403626k.
Der volle Inhalt der QuelleHodgson, David M., Christopher I. Pearson und Madiha Kazmi. „ChemInform Abstract: Generation and Electrophile Trapping of N-Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines.“ ChemInform 45, Nr. 29 (03.07.2014): no. http://dx.doi.org/10.1002/chin.201429118.
Der volle Inhalt der QuelleDidier, Dorian, und Felix Reiners. „Uncommon Four‐Membered Building Blocks – Cyclobutenes, Azetines and Thietes“. Chemical Record 21, Nr. 5 (18.03.2021): 1144–60. http://dx.doi.org/10.1002/tcr.202100011.
Der volle Inhalt der QuelleBaumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw und Dorian Didier. „Correction to Methods for the Synthesis of Substituted Azetines“. Organic Letters 19, Nr. 24 (22.11.2017): 6763. http://dx.doi.org/10.1021/acs.orglett.7b03520.
Der volle Inhalt der QuelleDejaegher, Yves, Sven Mangelinckx und Norbert De Kimpe. „Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines“. Journal of Organic Chemistry 67, Nr. 7 (April 2002): 2075–81. http://dx.doi.org/10.1021/jo010914j.
Der volle Inhalt der QuelleMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman und Michael P. Doyle. „Synthesis of Chiral Tetrasubstituted Azetidines from Donor–Acceptor Azetines via Asymmetric Copper(I)‐Catalyzed Imido‐Ylide [3+1]‐Cycloaddition with Metallo‐Enolcarbenes“. Angewandte Chemie International Edition 58, Nr. 45 (24.09.2019): 16188–92. http://dx.doi.org/10.1002/anie.201909929.
Der volle Inhalt der QuelleMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman und Michael P. Doyle. „Synthesis of Chiral Tetrasubstituted Azetidines from Donor–Acceptor Azetines via Asymmetric Copper(I)‐Catalyzed Imido‐Ylide [3+1]‐Cycloaddition with Metallo‐Enolcarbenes“. Angewandte Chemie 131, Nr. 45 (24.09.2019): 16334–38. http://dx.doi.org/10.1002/ange.201909929.
Der volle Inhalt der QuelleDejaegher, Yves, Sven Mangelinckx und Norbert De Kimpe. „ChemInform Abstract: Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines.“ ChemInform 33, Nr. 36 (20.05.2010): no. http://dx.doi.org/10.1002/chin.200236110.
Der volle Inhalt der QuelleMacNevin, Christopher J., Rhonda L. Moore und Dennis C. Liotta. „Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β-Amino Acid Derivatives“. Journal of Organic Chemistry 73, Nr. 4 (Februar 2008): 1264–69. http://dx.doi.org/10.1021/jo7018202.
Der volle Inhalt der QuelleDissertationen zum Thema "Azetines"
Luheshi, Abdul-Basset Nuri. „Cycloadditions to 1-azetines and 1-azetin-4-ones“. Thesis, University of Salford, 1988. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327973.
Der volle Inhalt der QuelleHemming, Karl. „Studies in the chemistry of 1-azetines and 1-azetin-4-ones“. Thesis, University of Salford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334307.
Der volle Inhalt der QuelleO'Gorman, P. A. „Some aspects of the chemistry of small ring organic molecules : 1-azetines, 1-azetidinones, 3-oxo-β-sultams and cyclopropenones“. Thesis, University of Huddersfield, 2009. http://eprints.hud.ac.uk/id/eprint/6310/.
Der volle Inhalt der QuellePitard, Arnaud. „1-azetines, 1,2-thiazetin-1,1-dioxides and isothiazol-1,1-dioxides as building blocks in heterocyclic synthesis : the attempted synthesis of bicyclic β-sultams“. Thesis, University of Huddersfield, 2009. http://eprints.hud.ac.uk/id/eprint/7061/.
Der volle Inhalt der QuelleLosa, Romain. „Organocatalyse redox par les phosphines : découverte de nouvelles transformations et vers le développement d'une version électrocatalytique“. Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASF014.
Der volle Inhalt der QuelleThis thesis work focused on organocatalysis using trivalent phosphines, compounds which play a crucial role in many chemical transformations and widely used for several organic syntheses. One of the two research axes of this thesis focused on the innovative development of organocatalytic methodologies using trivalent phosphines. We focused on P(III)/P(III) or P(III)/P(V) processes for the synthesis of oxygen or nitrogen-containing heterocycles. After developing a version stoichiometric in phosphine, the methodology was optimized by making it catalytic. A more detailed study enabling the synthesis of 2-azetine derivatives, promoted and then catalysed by phosphines, was developed during this thesis. The products thus obtained were valued in organic synthesis and tested biologically. Finally, the second line of research in this thesis focused directly on the electroreduction of phosphine oxides. In today's environmental context, it is imperative to render the reactions promoted by phosphine catalytic in phosphine, by introducing a reducing agent into the reaction medium. In order to progress towards the development of electrocatalytic reactions, we used electrochemistry for the reduction of phosphine oxides, thus inscribing our work in a more virtuous chemistry approach
Pearson, Christopher I. „Lithiated azetidine and azetine chemistry“. Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:cf3c942f-80de-4092-a38d-11006ccbb9ce.
Der volle Inhalt der QuelleYoshizawa, Akina. „Azetidines for asymmetric synthesis“. Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8719/.
Der volle Inhalt der QuelleThaxton, Amber. „Synthesis of Novel Azetidines“. ScholarWorks@UNO, 2013. http://scholarworks.uno.edu/td/1764.
Der volle Inhalt der QuelleKloesges, Johannes. „Novel Chemistry of aziridines and azetidines“. Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509969.
Der volle Inhalt der QuellePancholi, Alpa Kishor. „Synthesis of substituted azetidines and spirocyclic diazetidines“. Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/102606/.
Der volle Inhalt der QuelleBücher zum Thema "Azetines"
Luheshi, Abdul-Basset Nuri. Cycloadditions to 1-Azetines and 1-Azetin-4-ones. Salford: University of Salford, 1988.
Den vollen Inhalt der Quelle findenHemming, Karl. Studies in the chemistry of 1-azetines and 1-azetin-4-ones. Salford: University of Salford, 1993.
Den vollen Inhalt der Quelle findenKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Den vollen Inhalt der Quelle findenKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Azetines"
Khlebnikov, Alexander F., und Mikhail S. Novikov. „Ring Expansions of Azirines and Azetines“. In Topics in Heterocyclic Chemistry, 143–232. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_154.
Der volle Inhalt der QuelleMoore, James A., und Rita Seelig Ayers. „Azetidines“. In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 1–217. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187197.ch1.
Der volle Inhalt der QuelleLi, Jie Jack, und Minmin Yang. „Azetidines“. In Drug Discovery with Privileged Building Blocks, 29–32. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-3.
Der volle Inhalt der QuelleCouty, François, und Olivier R. P. David. „Ring Expansions of Nonactivated Aziridines and Azetidines“. In Topics in Heterocyclic Chemistry, 1–47. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_146.
Der volle Inhalt der QuelleGhorai, Manas K., Aditya Bhattacharyya, Subhomoy Das und Navya Chauhan. „Ring Expansions of Activated Aziridines and Azetidines“. In Topics in Heterocyclic Chemistry, 49–142. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_159.
Der volle Inhalt der QuelleBeatriz, Adilson, Mirta Gladis Mondino und Dênis Pires de Lima. „Lactams, Azetidines, Penicillins, and Cephalosporins: An Overview on the Synthesis and Their Antibacterial Activity“. In N-Heterocycles, 97–142. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_3.
Der volle Inhalt der QuelleSingh, G. S., M. D’hooghe und N. De Kimpe. „Azetidines, Azetines and Azetes: Monocyclic“. In Comprehensive Heterocyclic Chemistry III, 1–110. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00201-7.
Der volle Inhalt der Quellede Kimpe, Norbert. „Azetidines, Azetines, and Azetes: Monocyclic“. In Comprehensive Heterocyclic Chemistry II, 507–89. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00018-6.
Der volle Inhalt der QuelleAndresini, Michael, Leonardo Degennaro und Renzo Luisi. „Azetidines, Azetines and Azetes: Monocyclic“. In Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-818655-8.00155-4.
Der volle Inhalt der QuelleMehta, L. K., und J. Parrick. „Other Fused Azetidines, Azetines and Azetes“. In Comprehensive Heterocyclic Chemistry III, 239–319. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00204-2.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Azetines"
Kaufman, Teodoro, und Marcela Amongero. „ORGANOCATALYTIC APPROACH TO THE SYNTHESIS OF OPTICALLY ACTIVE 1,2,3-TRISUBSTITUTED AZETIDINES“. In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00211.
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