Gotowa bibliografia na temat „Azetines”
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Artykuły w czasopismach na temat "Azetines"
Baumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw i Dorian Didier. "Methods for the Synthesis of Substituted Azetines". Organic Letters 19, nr 20 (4.10.2017): 5681–84. http://dx.doi.org/10.1021/acs.orglett.7b02847.
Pełny tekst źródłaHodgson, David M., Christopher I. Pearson i 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.
Pełny tekst źródłaHodgson, David M., Christopher I. Pearson i 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 (3.07.2014): no. http://dx.doi.org/10.1002/chin.201429118.
Pełny tekst źródłaDidier, Dorian, i 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.
Pełny tekst źródłaBaumann, Andreas N., Michael Eisold, Arif Music, Geoffrey Haas, Yu Min Kiw i 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.
Pełny tekst źródłaDejaegher, Yves, Sven Mangelinckx i Norbert De Kimpe. "Rearrangement of 2-Aryl-3,3-dichloroazetidines: Intermediacy of 2-Azetines". Journal of Organic Chemistry 67, nr 7 (kwiecień 2002): 2075–81. http://dx.doi.org/10.1021/jo010914j.
Pełny tekst źródłaMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman i 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.
Pełny tekst źródłaMarichev, Kostiantyn O., Kan Wang, Kuiyong Dong, Nicole Greco, Lynée A. Massey, Yongming Deng, Hadi Arman i 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.
Pełny tekst źródłaDejaegher, Yves, Sven Mangelinckx i 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.
Pełny tekst źródłaMacNevin, Christopher J., Rhonda L. Moore i Dennis C. Liotta. "Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β-Amino Acid Derivatives". Journal of Organic Chemistry 73, nr 4 (luty 2008): 1264–69. http://dx.doi.org/10.1021/jo7018202.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaHemming, 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.
Pełny tekst źródłaO'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/.
Pełny tekst źródłaPitard, 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/.
Pełny tekst źródłaLosa, 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.
Pełny tekst źródłaThis 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.
Pełny tekst źródłaYoshizawa, Akina. "Azetidines for asymmetric synthesis". Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8719/.
Pełny tekst źródłaThaxton, Amber. "Synthesis of Novel Azetidines". ScholarWorks@UNO, 2013. http://scholarworks.uno.edu/td/1764.
Pełny tekst źródłaKloesges, Johannes. "Novel Chemistry of aziridines and azetidines". Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509969.
Pełny tekst źródłaPancholi, Alpa Kishor. "Synthesis of substituted azetidines and spirocyclic diazetidines". Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/102606/.
Pełny tekst źródłaKsiążki na temat "Azetines"
Luheshi, Abdul-Basset Nuri. Cycloadditions to 1-Azetines and 1-Azetin-4-ones. Salford: University of Salford, 1988.
Znajdź pełny tekst źródłaHemming, Karl. Studies in the chemistry of 1-azetines and 1-azetin-4-ones. Salford: University of Salford, 1993.
Znajdź pełny tekst źródłaKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Znajdź pełny tekst źródłaKaur, Navjeet. Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023.
Znajdź pełny tekst źródłaCzęści książek na temat "Azetines"
Khlebnikov, Alexander F., i Mikhail S. Novikov. "Ring Expansions of Azirines and Azetines". W Topics in Heterocyclic Chemistry, 143–232. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_154.
Pełny tekst źródłaMoore, James A., i Rita Seelig Ayers. "Azetidines". W 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.
Pełny tekst źródłaLi, Jie Jack, i Minmin Yang. "Azetidines". W Drug Discovery with Privileged Building Blocks, 29–32. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-3.
Pełny tekst źródłaCouty, François, i Olivier R. P. David. "Ring Expansions of Nonactivated Aziridines and Azetidines". W Topics in Heterocyclic Chemistry, 1–47. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_146.
Pełny tekst źródłaGhorai, Manas K., Aditya Bhattacharyya, Subhomoy Das i Navya Chauhan. "Ring Expansions of Activated Aziridines and Azetidines". W Topics in Heterocyclic Chemistry, 49–142. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_159.
Pełny tekst źródłaBeatriz, Adilson, Mirta Gladis Mondino i Dênis Pires de Lima. "Lactams, Azetidines, Penicillins, and Cephalosporins: An Overview on the Synthesis and Their Antibacterial Activity". W N-Heterocycles, 97–142. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_3.
Pełny tekst źródłaSingh, G. S., M. D’hooghe i N. De Kimpe. "Azetidines, Azetines and Azetes: Monocyclic". W Comprehensive Heterocyclic Chemistry III, 1–110. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00201-7.
Pełny tekst źródłade Kimpe, Norbert. "Azetidines, Azetines, and Azetes: Monocyclic". W Comprehensive Heterocyclic Chemistry II, 507–89. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00018-6.
Pełny tekst źródłaAndresini, Michael, Leonardo Degennaro i Renzo Luisi. "Azetidines, Azetines and Azetes: Monocyclic". W Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-818655-8.00155-4.
Pełny tekst źródłaMehta, L. K., i J. Parrick. "Other Fused Azetidines, Azetines and Azetes". W Comprehensive Heterocyclic Chemistry III, 239–319. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00204-2.
Pełny tekst źródłaStreszczenia konferencji na temat "Azetines"
Kaufman, Teodoro, i Marcela Amongero. "ORGANOCATALYTIC APPROACH TO THE SYNTHESIS OF OPTICALLY ACTIVE 1,2,3-TRISUBSTITUTED AZETIDINES". W 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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