Artículos de revistas sobre el tema "Azetines"
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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 completoHemming, Karl, Musharraf N. Khan, Paul A. O'Gorman y Arnaud Pitard. "1,2,4-Oxadiazoles from cycloreversions of oxadiazabicyclo[3.2.0]heptenes: 1-azetines as thiocyanate equivalents". Tetrahedron 69, n.º 4 (enero de 2013): 1279–84. http://dx.doi.org/10.1016/j.tet.2012.12.007.
Texto completoLuheshi, Abdul-Basset N., Robert K. Smalley, P. D. Kennewell y R. Westwood. "1,3-Dipolar cycloadditions of 2-ethoxy- and 2-(ethylthio)-1-azetines with nitrilimines". Tetrahedron Letters 31, n.º 1 (enero de 1990): 127–30. http://dx.doi.org/10.1016/s0040-4039(00)94352-1.
Texto completoGiubellina, Nicola, Wim Aelterman y Norbert De Kimpe. "Use of 3-halo-1-azaallylic anions in heterocyclic chemistry". Pure and Applied Chemistry 75, n.º 10 (1 de enero de 2003): 1433–42. http://dx.doi.org/10.1351/pac200375101433.
Texto completoHara, Shunya y Shigekazu Ito. "TiCl 4 ‐Mediated [2+2] Cycloaddition for Synthesis of Isolable CF 3 ‐Substituted 2‐Azetines". Asian Journal of Organic Chemistry 10, n.º 4 (17 de marzo de 2021): 788–92. http://dx.doi.org/10.1002/ajoc.202100082.
Texto completoLopez, Steven A. y K. N. Houk. "Substituent Effects on Rates and Torquoselectivities of Electrocyclic Ring-Openings of N-Substituted 2-Azetines". Journal of Organic Chemistry 79, n.º 13 (12 de junio de 2014): 6189–95. http://dx.doi.org/10.1021/jo500919s.
Texto completoMangelinckx, Sven, Veronique Van Speybroeck, Peter Vansteenkiste, Michel Waroquier y Norbert De Kimpe. "Experimental and Computational Study of the Conrotatory Ring Opening of Various 3-Chloro-2-azetines". Journal of Organic Chemistry 73, n.º 14 (julio de 2008): 5481–88. http://dx.doi.org/10.1021/jo800522b.
Texto completoBarluenga, José, Lorena Riesgo, Giacomo Lonzi, Miguel Tomás y Luis A. López. "Copper(I)-Catalyzed [3+1] Cycloaddition of Alkenyldiazoacetates and Iminoiodinanes: Easy Access to Substituted 2-Azetines". Chemistry - A European Journal 18, n.º 30 (21 de junio de 2012): 9221–24. http://dx.doi.org/10.1002/chem.201200998.
Texto completoSantos, Bruna S., Ana L. Cardoso, Ana Matos Beja, Manuela Ramos Silva, José A. Paixão, Francisco Palacios y Teresa M. V. D. Pinho e Melo. "Diastereoselective Aza-Baylis-Hillman Reactions: Synthesis of Chiral α-Allenylamines and 2-Azetines from Allenic Esters". European Journal of Organic Chemistry 2010, n.º 17 (30 de abril de 2010): 3249–56. http://dx.doi.org/10.1002/ejoc.200901415.
Texto completoSingh, Atul K., Ruchi Chawla y Lal Dhar S. Yadav. "Retracted article: Convenient access to strained trisubstituted 2-azetines from enals and chloramine-T in aqueous media". Green Chemistry 14, n.º 12 (2012): 3325. http://dx.doi.org/10.1039/c2gc36331c.
Texto completoLuheshi, Abdul-Basset N., Robert K. Smalley, Peter D. Kennewell y Robert Westwood. "1,3-Dipolar cycloadditions of 2-ethoxy- and 2-(ethylthio)-1-azetines with nitrile oxides and nitrile ylides". Tetrahedron Letters 31, n.º 1 (enero de 1990): 123–26. http://dx.doi.org/10.1016/s0040-4039(00)94351-x.
Texto completoSingh, Atul K., Ruchi Chawla y Lal Dhar S. Yadav. "ChemInform Abstract: Convenient Access to Strained Trisubstituted 2-Azetines from Enals and Chloramine-T in Aqueous Media." ChemInform 44, n.º 15 (25 de marzo de 2013): no. http://dx.doi.org/10.1002/chin.201315087.
Texto completoSantos, Bruna S., Ana L. Cardoso, Ana Matos Beja, Manuela Ramos Silva, Jose A. Paixao, Francisco Palacios y Teresa M. V. D. Pinho e Melo. "ChemInform Abstract: Diastereoselective Aza-Baylis-Hillman Reactions: Synthesis of Chiral α-Allenylamines and 2-Azetines from Allenic Esters." ChemInform 41, n.º 44 (7 de octubre de 2010): no. http://dx.doi.org/10.1002/chin.201044029.
Texto completoBarluenga, Jose, Lorena Riesgo, Giacomo Lonzi, Miguel Tomas y Luis A. Lopez. "ChemInform Abstract: Copper(I)-Catalyzed [3 + 1] Cycloaddition of Alkenyldiazoacetates and Iminoiodinanes: Easy Access to Substituted 2-Azetines." ChemInform 43, n.º 50 (29 de noviembre de 2012): no. http://dx.doi.org/10.1002/chin.201250101.
Texto completoFunes-Ardoiz, Ignacio, Jairo González, Javier Santamaría y Diego Sampedro. "Understanding the Mechanism of the Divergent Reactivity of Non-Heteroatom-Stabilized Chromium Carbene Complexes with Furfural Imines: Formation of Benzofurans and Azetines". Journal of Organic Chemistry 81, n.º 4 (4 de febrero de 2016): 1565–70. http://dx.doi.org/10.1021/acs.joc.5b02729.
Texto completoShindoh, Naoya, Kazuo Kitaura, Yoshiji Takemoto y Kiyosei Takasu. "Catalyst-Controlled Torquoselectivity Switch in the 4π Ring-Opening Reaction of 2-Amino-2-azetines Giving β-Substituted α,β-Unsaturated Amidines". Journal of the American Chemical Society 133, n.º 22 (8 de junio de 2011): 8470–73. http://dx.doi.org/10.1021/ja202576e.
Texto completoMarchand, Alan P., D. Rajagopal, Simon G. Bott y Thomas G. Archibald. "Reactions of 1-ethyl-3-azabicyclo[1.1.0]butane with electrophiles. A facile entry into new, N-substituted 3-ethylideneazetidines and 2-azetines". Journal of Organic Chemistry 59, n.º 7 (abril de 1994): 1608–12. http://dx.doi.org/10.1021/jo00086a008.
Texto completoHemming, Karl, Paul A. O’Gorman y Michael I. Page. "The synthesis of azabicyclo[4.2.1]nonenes by the addition of a cyclopropenone to 4-vinyl substituted 1-azetines—isomers of the homotropane nucleus". Tetrahedron Letters 47, n.º 4 (enero de 2006): 425–28. http://dx.doi.org/10.1016/j.tetlet.2005.11.081.
Texto completoHemming, Karl, Abdul-Bassett N. Luheshi, Alan D. Redhouse, Robert K. Smalley, J. Robin Thompson, Peter D. Kennewell y R. Westwood. "1,3-dipolar cycloadditions of 2-Ethoxy- and 2-(ethylthio)-1-azetines with nitrile oxides, nitrile ylides and nitrilimines: An unexpected 1,2,4-triazole formation." Tetrahedron 49, n.º 20 (enero de 1993): 4383–408. http://dx.doi.org/10.1016/s0040-4020(01)85755-0.
Texto completoJung, Michael E. y Yong Mi Choi. "New synthesis of 2-azetines and 1-azabutadienes and the use of the latter in Diels-Alder reactions: total synthesis of (.+-.)-.delta.-coniceine". Journal of Organic Chemistry 56, n.º 24 (noviembre de 1991): 6729–30. http://dx.doi.org/10.1021/jo00024a001.
Texto completoMARCHAND, A. P., D. RAJAGOPAL, S. G. BOTT y T. G. ARCHIBALD. "ChemInform Abstract: Reactions of 1-Aza-3-ethylbicyclo(1.1.0)butane with Electrophiles. A Facile Entry into New, N-Substituted 3-Ethylideneazetidines and 2- Azetines." ChemInform 25, n.º 36 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199436134.
Texto completoJUNG, M. E. y Y. M. CHOI. "ChemInform Abstract: New Synthesis of 2-Azetines and 1-Azabutadienes and the Use of the Latter in Diels-Alder Reactions: Total Synthesis of (.+-.)-δ- Coniceine." ChemInform 23, n.º 18 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199218169.
Texto completoHEMMING, K., A. B. N. LUHESHI, A. D. REDHOUSE, R. K. SMALLEY, J. R. THOMPSON, P. D. KENNEWELL y R. WESTWOOD. "ChemInform Abstract: 1,3-Dipolar Cycloadditions of 2-Ethoxy- and 2-(Ethylthio)-1-azetines with Nitrile Oxides, Nitrile Ylides and Nitrilimines: An Unexpected 1, 2,4-Triazole Formation." ChemInform 24, n.º 39 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199339086.
Texto completoYan, Hao, Xincheng Li, Chunxiang Wang y Boshun Wan. "Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines". Organic Chemistry Frontiers 4, n.º 9 (2017): 1833–38. http://dx.doi.org/10.1039/c7qo00405b.
Texto completoMughal, Haseeb y Michal Szostak. "Recent advances in the synthesis and reactivity of azetidines: strain-driven character of the four-membered heterocycle". Organic & Biomolecular Chemistry 19, n.º 15 (2021): 3274–86. http://dx.doi.org/10.1039/d1ob00061f.
Texto completoReidl, Tyler W. y Laura L. Anderson. "Divergent Functionalizations of Azetidines and Unsaturated Azetidines". Asian Journal of Organic Chemistry 8, n.º 7 (3 de junio de 2019): 931–45. http://dx.doi.org/10.1002/ajoc.201900229.
Texto completoBrianna Barbu. "Azetidines, assemble!" C&EN Global Enterprise 102, n.º 20 (1 de julio de 2024): 5. http://dx.doi.org/10.1021/cen-10220-scicon7.
Texto completoMehra, Vishu, Isha Lumb, Amit Anand y Vipan Kumar. "Recent advances in synthetic facets of immensely reactive azetidines". RSC Adv. 7, n.º 72 (2017): 45763–83. http://dx.doi.org/10.1039/c7ra08884a.
Texto completoPeipiņš, Vilnis, Krista Suta y Māris Turks. "Study on Synthesis of N-Protected 2-Triazolyl Azetidines". Key Engineering Materials 762 (febrero de 2018): 19–24. http://dx.doi.org/10.4028/www.scientific.net/kem.762.19.
Texto completoFawcett, Alexander. "Recent advances in the chemistry of bicyclo- and 1-azabicyclo[1.1.0]butanes". Pure and Applied Chemistry 92, n.º 5 (26 de mayo de 2020): 751–65. http://dx.doi.org/10.1515/pac-2019-1007.
Texto completoGhorai, Manas K., Subhomoy Das, Kalpataru Das y Amit Kumar. "Stereoselective synthesis of activated 2-arylazetidines via imino-aldol reaction". Organic & Biomolecular Chemistry 13, n.º 34 (2015): 9042–49. http://dx.doi.org/10.1039/c5ob01140j.
Texto completoMusci, Pantaleo, Marco Colella, Angela Altomare, Giuseppe Romanazzi, Nadeem S. Sheikh, Leonardo Degennaro y Renzo Luisi. "Dynamic Phenomena and Complexation Effects in the α-Lithiation and Asymmetric Functionalization of Azetidines". Molecules 27, n.º 9 (29 de abril de 2022): 2847. http://dx.doi.org/10.3390/molecules27092847.
Texto completoVinayak, Sumiti, Rajiv S. Jumani, Peter Miller, Muhammad M. Hasan, Briana I. McLeod, Jayesh Tandel, Erin E. Stebbins et al. "Bicyclic azetidines kill the diarrheal pathogen Cryptosporidium in mice by inhibiting parasite phenylalanyl-tRNA synthetase". Science Translational Medicine 12, n.º 563 (30 de septiembre de 2020): eaba8412. http://dx.doi.org/10.1126/scitranslmed.aba8412.
Texto completoRoy, Tony, Sachin Suresh Bhojgude, Trinadh Kaicharla, Manikandan Thangaraj, Bikash Garai y Akkattu T. Biju. "Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines". Organic Chemistry Frontiers 3, n.º 1 (2016): 71–76. http://dx.doi.org/10.1039/c5qo00328h.
Texto completoParmar, Dixit, Lena Henkel, Josef Dib y Magnus Rueping. "Iron catalysed cross-couplings of azetidines – application to the formal synthesis of a pharmacologically active molecule". Chemical Communications 51, n.º 11 (2015): 2111–13. http://dx.doi.org/10.1039/c4cc09337b.
Texto completoGomathy, Subramanian. "MOLECULAR DOCKING STUDIES, IN SILICO ADMET SCREENING OF SELECTED NOVEL AZETIDINE SUBSTITUTED NAPHTHALENE’S TARGETING PROTEASE ENZYME AGAINST SARS COV-19". Journal of Medical pharmaceutical and allied sciences 10, n.º 6 (15 de noviembre de 2021): 3986–91. http://dx.doi.org/10.22270/jmpas.v10i6.2505.
Texto completoAndresini, Michael, Leonardo Degennaro y Renzo Luisi. "The renaissance of strained 1-azabicyclo[1.1.0]butanes as useful reagents for the synthesis of functionalized azetidines". Organic & Biomolecular Chemistry 18, n.º 30 (2020): 5798–810. http://dx.doi.org/10.1039/d0ob01251c.
Texto completoDave, Paritosh R., Rajagopal Duddu, Rao Surapaneni y Richard Gilardi. "Diels-Alder reactions ofN-acetyl-2-azetine". Tetrahedron Letters 40, n.º 3 (enero de 1999): 443–46. http://dx.doi.org/10.1016/s0040-4039(98)02506-4.
Texto completoCrunkhorn, Sarah. "Bicyclic azetidines treat cryptosporidiosis". Nature Reviews Drug Discovery 19, n.º 12 (2 de noviembre de 2020): 838. http://dx.doi.org/10.1038/d41573-020-00193-y.
Texto completoChristmann, M., R. de Figueiredo y R. Fröhlich. "Synthesis of Chiral Azetidines". Synfacts 2006, n.º 9 (septiembre de 2006): 0879. http://dx.doi.org/10.1055/s-2006-942066.
Texto completoAntermite, Daniele, Leonardo Degennaro y Renzo Luisi. "Recent advances in the chemistry of metallated azetidines". Organic & Biomolecular Chemistry 15, n.º 1 (2017): 34–50. http://dx.doi.org/10.1039/c6ob01665k.
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