Literatura científica selecionada sobre o tema "Azetines"
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Artigos de revistas sobre o assunto "Azetines"
Baumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw e Dorian Didier. "Methods for the Synthesis of Substituted Azetines". Organic Letters 19, n.º 20 (4 de outubro de 2017): 5681–84. http://dx.doi.org/10.1021/acs.orglett.7b02847.
Texto completo da fonteHodgson, David M., Christopher I. Pearson e 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 janeiro de 2014): 856–59. http://dx.doi.org/10.1021/ol403626k.
Texto completo da fonteHodgson, David M., Christopher I. Pearson e 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 julho de 2014): no. http://dx.doi.org/10.1002/chin.201429118.
Texto completo da fonteDidier, Dorian, e Felix Reiners. "Uncommon Four‐Membered Building Blocks – Cyclobutenes, Azetines and Thietes". Chemical Record 21, n.º 5 (18 de março de 2021): 1144–60. http://dx.doi.org/10.1002/tcr.202100011.
Texto completo da fonteBaumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw e Dorian Didier. "Correction to Methods for the Synthesis of Substituted Azetines". Organic Letters 19, n.º 24 (22 de novembro de 2017): 6763. http://dx.doi.org/10.1021/acs.orglett.7b03520.
Texto completo da fonteDejaegher, Yves, Sven Mangelinckx e 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 completo da fonteMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman e 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 setembro de 2019): 16188–92. http://dx.doi.org/10.1002/anie.201909929.
Texto completo da fonteMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman e 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 setembro de 2019): 16334–38. http://dx.doi.org/10.1002/ange.201909929.
Texto completo da fonteDejaegher, Yves, Sven Mangelinckx e Norbert De Kimpe. "ChemInform Abstract: Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines." ChemInform 33, n.º 36 (20 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200236110.
Texto completo da fonteMacNevin, Christopher J., Rhonda L. Moore e Dennis C. Liotta. "Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β-Amino Acid Derivatives". Journal of Organic Chemistry 73, n.º 4 (fevereiro de 2008): 1264–69. http://dx.doi.org/10.1021/jo7018202.
Texto completo da fonteTeses / dissertações sobre o assunto "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 completo da fonteHemming, 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 completo da fonteO'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 completo da fontePitard, 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 completo da fonteLosa, 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 completo da fonteThis 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 completo da fonteYoshizawa, Akina. "Azetidines for asymmetric synthesis". Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8719/.
Texto completo da fonteThaxton, Amber. "Synthesis of Novel Azetidines". ScholarWorks@UNO, 2013. http://scholarworks.uno.edu/td/1764.
Texto completo da fonteKloesges, Johannes. "Novel Chemistry of aziridines and azetidines". Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509969.
Texto completo da fontePancholi, Alpa Kishor. "Synthesis of substituted azetidines and spirocyclic diazetidines". Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/102606/.
Texto completo da fonteLivros sobre o assunto "Azetines"
Luheshi, Abdul-Basset Nuri. Cycloadditions to 1-Azetines and 1-Azetin-4-ones. Salford: University of Salford, 1988.
Encontre o texto completo da fonteHemming, Karl. Studies in the chemistry of 1-azetines and 1-azetin-4-ones. Salford: University of Salford, 1993.
Encontre o texto completo da fonteKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Encontre o texto completo da fonteKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Azetines"
Khlebnikov, Alexander F., e 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.
Texto completo da fonteMoore, James A., e 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.
Texto completo da fonteLi, Jie Jack, e 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.
Texto completo da fonteCouty, François, e 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.
Texto completo da fonteGhorai, Manas K., Aditya Bhattacharyya, Subhomoy Das e 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.
Texto completo da fonteBeatriz, Adilson, Mirta Gladis Mondino e 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.
Texto completo da fonteSingh, G. S., M. D’hooghe e 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.
Texto completo da fontede 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.
Texto completo da fonteAndresini, Michael, Leonardo Degennaro e 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.
Texto completo da fonteMehta, L. K., e 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.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Azetines"
Kaufman, Teodoro, e 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.
Texto completo da fonte