Добірка наукової літератури з теми "Azetines"
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Статті в журналах з теми "Azetines":
Baumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw, and Dorian Didier. "Methods for the Synthesis of Substituted Azetines." Organic Letters 19, no. 20 (October 4, 2017): 5681–84. http://dx.doi.org/10.1021/acs.orglett.7b02847.
Hodgson, David M., Christopher I. Pearson, and Madiha Kazmi. "Generation and Electrophile Trapping of N-Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines." Organic Letters 16, no. 3 (January 10, 2014): 856–59. http://dx.doi.org/10.1021/ol403626k.
Hodgson, David M., Christopher I. Pearson, and Madiha Kazmi. "ChemInform Abstract: Generation and Electrophile Trapping of N-Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines." ChemInform 45, no. 29 (July 3, 2014): no. http://dx.doi.org/10.1002/chin.201429118.
Didier, Dorian, and Felix Reiners. "Uncommon Four‐Membered Building Blocks – Cyclobutenes, Azetines and Thietes." Chemical Record 21, no. 5 (March 18, 2021): 1144–60. http://dx.doi.org/10.1002/tcr.202100011.
Baumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw, and Dorian Didier. "Correction to Methods for the Synthesis of Substituted Azetines." Organic Letters 19, no. 24 (November 22, 2017): 6763. http://dx.doi.org/10.1021/acs.orglett.7b03520.
Dejaegher, Yves, Sven Mangelinckx, and Norbert De Kimpe. "Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines." Journal of Organic Chemistry 67, no. 7 (April 2002): 2075–81. http://dx.doi.org/10.1021/jo010914j.
Marichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman, and 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, no. 45 (September 24, 2019): 16188–92. http://dx.doi.org/10.1002/anie.201909929.
Marichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman, and 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, no. 45 (September 24, 2019): 16334–38. http://dx.doi.org/10.1002/ange.201909929.
Dejaegher, Yves, Sven Mangelinckx, and Norbert De Kimpe. "ChemInform Abstract: Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines." ChemInform 33, no. 36 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200236110.
MacNevin, Christopher J., Rhonda L. Moore та Dennis C. Liotta. "Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β-Amino Acid Derivatives". Journal of Organic Chemistry 73, № 4 (лютий 2008): 1264–69. http://dx.doi.org/10.1021/jo7018202.
Дисертації з теми "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.
Hemming, 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.
O'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/.
Pitard, 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/.
Losa, 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.
This 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.
Yoshizawa, Akina. "Azetidines for asymmetric synthesis." Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8719/.
Thaxton, Amber. "Synthesis of Novel Azetidines." ScholarWorks@UNO, 2013. http://scholarworks.uno.edu/td/1764.
Kloesges, Johannes. "Novel Chemistry of aziridines and azetidines." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509969.
Pancholi, Alpa Kishor. "Synthesis of substituted azetidines and spirocyclic diazetidines." Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/102606/.
Книги з теми "Azetines":
Luheshi, Abdul-Basset Nuri. Cycloadditions to 1-Azetines and 1-Azetin-4-ones. Salford: University of Salford, 1988.
Hemming, Karl. Studies in the chemistry of 1-azetines and 1-azetin-4-ones. Salford: University of Salford, 1993.
Kaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Kaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Частини книг з теми "Azetines":
Khlebnikov, Alexander F., and 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.
Moore, James A., and 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.
Li, Jie Jack, and 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.
Couty, François, and 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.
Ghorai, Manas K., Aditya Bhattacharyya, Subhomoy Das, and 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.
Beatriz, Adilson, Mirta Gladis Mondino, and 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.
Singh, G. S., M. D’hooghe, and 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.
de 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.
Andresini, Michael, Leonardo Degennaro, and 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.
Mehta, L. K., and 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.
Тези доповідей конференцій з теми "Azetines":
Kaufman, Teodoro, and 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.