Literatura académica sobre el tema "Azetines"
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Artículos de revistas sobre el tema "Azetines"
Baumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw y Dorian Didier. "Methods for the Synthesis of Substituted Azetines". Organic Letters 19, n.º 20 (4 de octubre de 2017): 5681–84. http://dx.doi.org/10.1021/acs.orglett.7b02847.
Texto completoHodgson, David M., Christopher I. Pearson y Madiha Kazmi. "Generation and Electrophile Trapping of N-Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines". Organic Letters 16, n.º 3 (10 de enero de 2014): 856–59. http://dx.doi.org/10.1021/ol403626k.
Texto completoHodgson, David M., Christopher I. Pearson y Madiha Kazmi. "ChemInform Abstract: Generation and Electrophile Trapping of N-Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines." ChemInform 45, n.º 29 (3 de julio de 2014): no. http://dx.doi.org/10.1002/chin.201429118.
Texto completoDidier, Dorian y Felix Reiners. "Uncommon Four‐Membered Building Blocks – Cyclobutenes, Azetines and Thietes". Chemical Record 21, n.º 5 (18 de marzo de 2021): 1144–60. http://dx.doi.org/10.1002/tcr.202100011.
Texto completoBaumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw y Dorian Didier. "Correction to Methods for the Synthesis of Substituted Azetines". Organic Letters 19, n.º 24 (22 de noviembre de 2017): 6763. http://dx.doi.org/10.1021/acs.orglett.7b03520.
Texto completoDejaegher, Yves, Sven Mangelinckx y Norbert De Kimpe. "Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines". Journal of Organic Chemistry 67, n.º 7 (abril de 2002): 2075–81. http://dx.doi.org/10.1021/jo010914j.
Texto completoMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman y 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, n.º 45 (24 de septiembre de 2019): 16188–92. http://dx.doi.org/10.1002/anie.201909929.
Texto completoMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman y 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, n.º 45 (24 de septiembre de 2019): 16334–38. http://dx.doi.org/10.1002/ange.201909929.
Texto completoDejaegher, Yves, Sven Mangelinckx y Norbert De Kimpe. "ChemInform Abstract: Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines." ChemInform 33, n.º 36 (20 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200236110.
Texto completoMacNevin, Christopher J., Rhonda L. Moore y Dennis C. Liotta. "Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β-Amino Acid Derivatives". Journal of Organic Chemistry 73, n.º 4 (febrero de 2008): 1264–69. http://dx.doi.org/10.1021/jo7018202.
Texto completoTesis sobre el tema "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.
Texto completoHemming, 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.
Texto completoO'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/.
Texto completoPitard, 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/.
Texto completoLosa, 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.
Texto completoThis 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.
Texto completoYoshizawa, Akina. "Azetidines for asymmetric synthesis". Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8719/.
Texto completoThaxton, Amber. "Synthesis of Novel Azetidines". ScholarWorks@UNO, 2013. http://scholarworks.uno.edu/td/1764.
Texto completoKloesges, Johannes. "Novel Chemistry of aziridines and azetidines". Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509969.
Texto completoPancholi, Alpa Kishor. "Synthesis of substituted azetidines and spirocyclic diazetidines". Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/102606/.
Texto completoLibros sobre el tema "Azetines"
Luheshi, Abdul-Basset Nuri. Cycloadditions to 1-Azetines and 1-Azetin-4-ones. Salford: University of Salford, 1988.
Buscar texto completoHemming, Karl. Studies in the chemistry of 1-azetines and 1-azetin-4-ones. Salford: University of Salford, 1993.
Buscar texto completoKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Buscar texto completoKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Buscar texto completoCapítulos de libros sobre el tema "Azetines"
Khlebnikov, Alexander F. y Mikhail S. Novikov. "Ring Expansions of Azirines and Azetines". En Topics in Heterocyclic Chemistry, 143–232. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_154.
Texto completoMoore, James A. y Rita Seelig Ayers. "Azetidines". En 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.
Texto completoLi, Jie Jack y Minmin Yang. "Azetidines". En Drug Discovery with Privileged Building Blocks, 29–32. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-3.
Texto completoCouty, François y Olivier R. P. David. "Ring Expansions of Nonactivated Aziridines and Azetidines". En Topics in Heterocyclic Chemistry, 1–47. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_146.
Texto completoGhorai, Manas K., Aditya Bhattacharyya, Subhomoy Das y Navya Chauhan. "Ring Expansions of Activated Aziridines and Azetidines". En Topics in Heterocyclic Chemistry, 49–142. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_159.
Texto completoBeatriz, Adilson, Mirta Gladis Mondino y Dênis Pires de Lima. "Lactams, Azetidines, Penicillins, and Cephalosporins: An Overview on the Synthesis and Their Antibacterial Activity". En N-Heterocycles, 97–142. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_3.
Texto completoSingh, G. S., M. D’hooghe y N. De Kimpe. "Azetidines, Azetines and Azetes: Monocyclic". En Comprehensive Heterocyclic Chemistry III, 1–110. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00201-7.
Texto completode Kimpe, Norbert. "Azetidines, Azetines, and Azetes: Monocyclic". En Comprehensive Heterocyclic Chemistry II, 507–89. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00018-6.
Texto completoAndresini, Michael, Leonardo Degennaro y Renzo Luisi. "Azetidines, Azetines and Azetes: Monocyclic". En Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-818655-8.00155-4.
Texto completoMehta, L. K. y J. Parrick. "Other Fused Azetidines, Azetines and Azetes". En Comprehensive Heterocyclic Chemistry III, 239–319. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00204-2.
Texto completoActas de conferencias sobre el tema "Azetines"
Kaufman, Teodoro y Marcela Amongero. "ORGANOCATALYTIC APPROACH TO THE SYNTHESIS OF OPTICALLY ACTIVE 1,2,3-TRISUBSTITUTED AZETIDINES". En 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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