Artigos de revistas sobre o tema "Donor-Acceptor cyclopropane"
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Craig, Alexander J., e Bill C. Hawkins. "The Bonding and Reactivity of α-Carbonyl Cyclopropanes". Synthesis 52, n.º 01 (1 de outubro de 2019): 27–39. http://dx.doi.org/10.1055/s-0039-1690695.
Texto completo da fonteBoichenko, Maksim A., Andrey Yu Plodukhin, Vitaly V. Shorokhov, Danyla S. Lebedev, Anastasya V. Filippova, Sergey S. Zhokhov, Elena A. Tarasenko, Victor B. Rybakov, Igor V. Trushkov e Olga A. Ivanova. "Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines". Molecules 27, n.º 23 (2 de dezembro de 2022): 8468. http://dx.doi.org/10.3390/molecules27238468.
Texto completo da fonteMead, Keith, e Yahaira Reyes. "Acetoxy-Substituted Cyclopropane Dicarbonyls as Stable Donor–Acceptor–Acceptor Cyclopropanes". Synthesis 47, n.º 19 (25 de junho de 2015): 3020–26. http://dx.doi.org/10.1055/s-0034-1379934.
Texto completo da fonteFadeev, Alexander A., Alexey O. Chagarovskiy, Anton S. Makarov, Irina I. Levina, Olga A. Ivanova, Maxim G. Uchuskin e Igor V. Trushkov. "Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones". Molecules 25, n.º 23 (5 de dezembro de 2020): 5748. http://dx.doi.org/10.3390/molecules25235748.
Texto completo da fonteGrover, Huck K., Michael R. Emmett e Michael A. Kerr. "Carbocycles from donor–acceptor cyclopropanes". Organic & Biomolecular Chemistry 13, n.º 3 (2015): 655–71. http://dx.doi.org/10.1039/c4ob02117g.
Texto completo da fonteReyes, Yahaira, e Keith T. Mead. "ChemInform Abstract: Acetoxy-Substituted Cyclopropane Dicarbonyls as Stable Donor-Acceptor-Acceptor Cyclopropanes." ChemInform 47, n.º 7 (janeiro de 2016): no. http://dx.doi.org/10.1002/chin.201607087.
Texto completo da fonteBudynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin e Mikhail Melnikov. "Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles". Synthesis 49, n.º 14 (18 de maio de 2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.
Texto completo da fonteIvanova, Olga, Vladimir Andronov, Irina Levina, Alexey Chagarovskiy, Leonid Voskressensky e Igor Trushkov. "Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates". Molecules 24, n.º 1 (24 de dezembro de 2018): 57. http://dx.doi.org/10.3390/molecules24010057.
Texto completo da fonteLiu, Haidong, Lifang Tian, Hui Wang, Zhi-Qiang Li, Chi Zhang, Fei Xue e Chao Feng. "A novel type of donor–acceptor cyclopropane with fluorine as the donor: (3 + 2)-cycloadditions with carbonyls". Chemical Science 13, n.º 9 (2022): 2686–91. http://dx.doi.org/10.1039/d2sc00302c.
Texto completo da fonteCavitt, Marchello A., Lien H. Phun e Stefan France. "Intramolecular donor–acceptor cyclopropane ring-opening cyclizations". Chem. Soc. Rev. 43, n.º 3 (2014): 804–18. http://dx.doi.org/10.1039/c3cs60238a.
Texto completo da fonteIvanova, Olga A., Vitaly V. Shorokhov, Ivan A. Andreev, Nina K. Ratmanova, Victor B. Rybakov, Elena D. Strel’tsova e Igor V. Trushkov. "Synthesis of 2-[2-(Ethoxymethoxy)phenyl]spiro[cyclopropane-1,2′-indene]-1′,3′-dione". Molbank 2023, n.º 1 (14 de março de 2023): M1604. http://dx.doi.org/10.3390/m1604.
Texto completo da fonteMlostoń, Grzegorz, Mateusz Kowalczyk, André U. Augustin, Peter G. Jones e Daniel B. Werz. "Ferrocenyl-substituted tetrahydrothiophenes via formal [3 + 2]-cycloaddition reactions of ferrocenyl thioketones with donor–acceptor cyclopropanes". Beilstein Journal of Organic Chemistry 16 (10 de junho de 2020): 1288–95. http://dx.doi.org/10.3762/bjoc.16.109.
Texto completo da fonteHayakawa, Kosuke, Shin-ichi Matsuoka e Masato Suzuki. "Ring-opening polymerization of donor–acceptor cyclopropanes catalyzed by Lewis acids". Polymer Chemistry 8, n.º 25 (2017): 3841–47. http://dx.doi.org/10.1039/c7py00794a.
Texto completo da fonteAugustin, André U., e Daniel B. Werz. "Exploiting Heavier Organochalcogen Compounds in Donor–Acceptor Cyclopropane Chemistry". Accounts of Chemical Research 54, n.º 6 (4 de março de 2021): 1528–41. http://dx.doi.org/10.1021/acs.accounts.1c00023.
Texto completo da fonteCavitt, Marchello A., Lien H. Phun e Stefan France. "ChemInform Abstract: Intramolecular Donor-Acceptor Cyclopropane Ring-Opening Cyclizations". ChemInform 45, n.º 17 (10 de abril de 2014): no. http://dx.doi.org/10.1002/chin.201417267.
Texto completo da fonteKreft, Alexander, Peter G. Jones e Daniel B. Werz. "The Cyclopropyl Group as a Neglected Donor in Donor–Acceptor Cyclopropane Chemistry". Organic Letters 20, n.º 7 (20 de março de 2018): 2059–62. http://dx.doi.org/10.1021/acs.orglett.8b00603.
Texto completo da fonteSliwinska, Anna, Wojciech Czardybon e John Warkentin. "Zwitterion from a Cyclopropane with Geminal Donor and Acceptor Groups". Organic Letters 9, n.º 4 (fevereiro de 2007): 695–98. http://dx.doi.org/10.1021/ol063021s.
Texto completo da fonteAlonso, Miguel E., Sarah V. Pekerar e Maria L. Borgo. "Transmission of electronic effects through 2-[donor]-1-[acceptor]-cyclopropane". Magnetic Resonance in Chemistry 28, n.º 11 (novembro de 1990): 956–62. http://dx.doi.org/10.1002/mrc.1260281110.
Texto completo da fonteCruz-Cabeza, Aurora J., e Frank H. Allen. "Geometry and conformation of cyclopropane derivatives having σ-acceptor and σ-donor substituents: a theoretical and crystal structure database study". Acta Crystallographica Section B Structural Science 68, n.º 2 (25 de fevereiro de 2012): 182–88. http://dx.doi.org/10.1107/s0108768111054991.
Texto completo da fonteAllen, F. H., J. P. M. Lommerse, V. J. Hoy, J. A. K. Howard e G. R. Desiraju. "The hydrogen-bond C–H donor and π-acceptor characteristics of three-membered rings". Acta Crystallographica Section B Structural Science 52, n.º 4 (1 de agosto de 1996): 734–45. http://dx.doi.org/10.1107/s0108768196005319.
Texto completo da fonteReissig, Hans-Ulrich, e Reinhold Zimmer. "Donor−Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis†". Chemical Reviews 103, n.º 4 (abril de 2003): 1151–96. http://dx.doi.org/10.1021/cr010016n.
Texto completo da fonteBeyzavi, M. Hassan, Carolin Nietzold, Hans-Ulrich Reissig e Arno Wiehe. "Synthesis of Functionalizedtrans-A2B2-Porphyrins Using Donor-Acceptor Cyclopropane-Derived Dipyrromethanes". Advanced Synthesis & Catalysis 355, n.º 7 (30 de abril de 2013): 1409–22. http://dx.doi.org/10.1002/adsc.201300141.
Texto completo da fonteZhang, Yanqun, Manyu Jin, Cunqi Wu, Yongxia Zhao, Hua Zhou e Jingwei Xu. "A practical and reusable catalyst for the synthesis of donor-acceptor cyclopropane". Catalysis Communications 103 (janeiro de 2018): 5–9. http://dx.doi.org/10.1016/j.catcom.2017.09.009.
Texto completo da fonteLevitskiy, Oleg A., Olga I. Aglamazova, Yuri K. Grishin e Tatiana V. Magdesieva. "Reductive opening of a cyclopropane ring in the Ni(II) coordination environment: a route to functionalized dehydroalanine and cysteine derivatives". Beilstein Journal of Organic Chemistry 18 (8 de setembro de 2022): 1166–76. http://dx.doi.org/10.3762/bjoc.18.121.
Texto completo da fonteMorales, Christian L., e Brian L. Pagenkopf. "Total Synthesis of (±)-Goniomitine via a Formal Nitrile/Donor−Acceptor Cyclopropane [3 + 2] Cyclization". Organic Letters 10, n.º 2 (janeiro de 2008): 157–59. http://dx.doi.org/10.1021/ol702376j.
Texto completo da fonteZheng, Xiaomei, e Michael A. Kerr. "Synthesis and Cross-Coupling Reactions of 7-Azaindoles via a New Donor−Acceptor Cyclopropane". Organic Letters 8, n.º 17 (agosto de 2006): 3777–79. http://dx.doi.org/10.1021/ol061379i.
Texto completo da fonteBrand, Christian, Gesche Rauch, Michele Zanoni, Birger Dittrich e Daniel B. Werz. "Synthesis of [n,5]-Spiroketals by Ring Enlargement of Donor-Acceptor-Substituted Cyclopropane Derivatives". Journal of Organic Chemistry 74, n.º 22 (20 de novembro de 2009): 8779–86. http://dx.doi.org/10.1021/jo901902g.
Texto completo da fonteBeyzavi, M. Hassan, Carolin Nietzold, Hans-Ulrich Reissig e Arno Wiehe. "ChemInform Abstract: Synthesis of Functionalized trans-A2B2-Porphyrins Using Donor-Acceptor Cyclopropane-Derived Dipyrromethanes." ChemInform 44, n.º 38 (30 de agosto de 2013): no. http://dx.doi.org/10.1002/chin.201338109.
Texto completo da fonteSabbatani, Juliette, e Nuno Maulide. "Temporary Generation of a Cyclopropyl Oxocarbenium Ion Enables Highly Diastereoselective Donor-Acceptor Cyclopropane Cycloaddition". Angewandte Chemie International Edition 55, n.º 23 (21 de abril de 2016): 6780–83. http://dx.doi.org/10.1002/anie.201601340.
Texto completo da fonteKang, Qikai, Lijia Wang, Zhongbo Zheng, Junfang Li e Yong Tang. "Sidearm as a Control in the Asymmetric Ring Opening Reaction of Donor-Acceptor Cyclopropane". Chinese Journal of Chemistry 32, n.º 8 (4 de abril de 2014): 669–72. http://dx.doi.org/10.1002/cjoc.201400053.
Texto completo da fonteLund, Elizabeth A., Isaac A. Kennedy e Alex G. Fallis. "Dihydrofurans from α-diazoketones due to facile ring opening – cyclization of donor–acceptor cyclopropane intermediates". Canadian Journal of Chemistry 74, n.º 12 (1 de dezembro de 1996): 2401–12. http://dx.doi.org/10.1139/v96-269.
Texto completo da fontePilsl, Ludwig K. A., Thomas Ertl e Oliver Reiser. "Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor–Acceptor Cyclopropane as Key Intermediate". Organic Letters 19, n.º 10 (9 de maio de 2017): 2754–57. http://dx.doi.org/10.1021/acs.orglett.7b01111.
Texto completo da fonteGharpure, Santosh J., Laxmi Narayan Nanda e Dimple Kumari. "Enantiospecific Total Synthesis of (+)-3-epi -Epohelmin A Using a Nitrogen-Substituted Donor-Acceptor Cyclopropane". European Journal of Organic Chemistry 2017, n.º 27 (18 de julho de 2017): 3917–20. http://dx.doi.org/10.1002/ejoc.201700498.
Texto completo da fonteAlford, Joshua S., e Huw M. L. Davies. "Expanding the Scope of Donor/Acceptor Carbenes to N-Phthalimido Donor Groups: Diastereoselective Synthesis of 1-Cyclopropane α-Amino Acids". Organic Letters 14, n.º 23 (15 de novembro de 2012): 6020–23. http://dx.doi.org/10.1021/ol3029127.
Texto completo da fonteGharpure, Santosh J., Laxmi Narayan Nanda e Manoj Kumar Shukla. "Donor–Acceptor Substituted Cyclopropane to Butanolide and Butenolide Natural Products: Enantiospecific First Total Synthesis of (+)-Hydroxyancepsenolide". Organic Letters 16, n.º 24 (8 de dezembro de 2014): 6424–27. http://dx.doi.org/10.1021/ol503246k.
Texto completo da fonteNovikov, Roman A., Anna V. Tarasova, Victor A. Korolev, Vladimir P. Timofeev e Yury V. Tomilov. "A New Type of Donor-Acceptor Cyclopropane Reactivity: The Generation of Formal 1,2- and 1,4-Dipoles". Angewandte Chemie 126, n.º 12 (19 de fevereiro de 2014): 3251–55. http://dx.doi.org/10.1002/ange.201306186.
Texto completo da fonteKang, Qikai, Lijia Wang, Zhongbo Zheng, Junfang Li e Yong Tang. "ChemInform Abstract: Sidearm as a Control in the Asymmetric Ring Opening Reaction of Donor-Acceptor Cyclopropane." ChemInform 46, n.º 8 (fevereiro de 2015): no. http://dx.doi.org/10.1002/chin.201508033.
Texto completo da fonteNovikov, Roman A., Anna V. Tarasova, Victor A. Korolev, Vladimir P. Timofeev e Yury V. Tomilov. "A New Type of Donor-Acceptor Cyclopropane Reactivity: The Generation of Formal 1,2- and 1,4-Dipoles". Angewandte Chemie International Edition 53, n.º 12 (19 de fevereiro de 2014): 3187–91. http://dx.doi.org/10.1002/anie.201306186.
Texto completo da fonteAlonso, Miguel E., e Sarah V. Pekerar. "Transmission of electronic effects through cyclopropane. II.—Comparative modulation of1H chemical shifts by aryloxy and aryl substituents in 2-(donor)-1-(acceptor)cyclopropanes". Magnetic Resonance in Chemistry 29, n.º 6 (junho de 1991): 587–93. http://dx.doi.org/10.1002/mrc.1260290609.
Texto completo da fonteXiao, Jun-An, Jie Li, Peng-Ju Xia, Zhao-Fang Zhou, Zhao-Xu Deng, Hao-Yue Xiang, Xiao-Qing Chen e Hua Yang. "Diastereoselective Intramolecular [3 + 2]-Annulation of Donor–Acceptor Cyclopropane with Imine-Assembling Hexahydropyrrolo[3,2-c]quinolinone Scaffolds". Journal of Organic Chemistry 81, n.º 22 (3 de novembro de 2016): 11185–94. http://dx.doi.org/10.1021/acs.joc.6b02172.
Texto completo da fonteLUND, E. A., I. A. KENNEDY e A. G. FALLIS. "ChemInform Abstract: Dihydrofurans from α-Diazoketones Due to Facile Ring Opening - Cyclization of Donor-Acceptor Cyclopropane Intermediates." ChemInform 28, n.º 27 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199727124.
Texto completo da fonteAlford, Joshua S., e Huw M. L. Davies. "ChemInform Abstract: Expanding the Scope of Donor/Acceptor Carbenes to N-Phthalimido Donor Groups: Diastereoselective Synthesis of 1-Cyclopropane α-Amino Acids." ChemInform 44, n.º 19 (18 de abril de 2013): no. http://dx.doi.org/10.1002/chin.201319048.
Texto completo da fonteGhosh, Asit, Subhajit Mandal, Pratim Kumar Chattaraj e Prabal Banerjee. "Ring Expansion of Donor–Acceptor Cyclopropane via Substituent Controlled Selective N-Transfer of Oxaziridine: Synthetic and Mechanistic Insights". Organic Letters 18, n.º 19 (29 de setembro de 2016): 4940–43. http://dx.doi.org/10.1021/acs.orglett.6b02417.
Texto completo da fonteNovikov, Roman A., Anna V. Tarasova, Victor A. Korolev, Vladimir P. Timofeev e Yury V. Tomilov. "ChemInform Abstract: A New Type of Donor-Acceptor Cyclopropane Reactivity: The Generation of Formal 1,2- and 1,4-Dipoles." ChemInform 45, n.º 36 (21 de agosto de 2014): no. http://dx.doi.org/10.1002/chin.201436034.
Texto completo da fonteVartanova, Anna E., Irina I. Levina, Victor B. Rybakov, Olga A. Ivanova e Igor V. Trushkov. "Donor–Acceptor Cyclopropane Ring Opening with 6-Amino-1,3-dimethyluracil and Its Use in Pyrimido[4,5-b]azepines Synthesis". Journal of Organic Chemistry 86, n.º 17 (12 de agosto de 2021): 12300–12308. http://dx.doi.org/10.1021/acs.joc.1c01064.
Texto completo da fonteYang, Hua, Jie Li, Jun-An Xiao, Shu-Juan Zhao e Hao-Yue Xiang. "Facile Construction of Pyrrolo[1,2-a]indolenine Scaffold via Diastereoselective [3+2] Annulation of Donor–Acceptor Cyclopropane with Indolenine". Synthesis 49, n.º 18 (19 de julho de 2017): 4292–98. http://dx.doi.org/10.1055/s-0036-1588876.
Texto completo da fonteMaslivetc, Vladimir A., Marina Rubina e Michael Rubin. "One-pot synthesis of GABA amides via the nucleophilic addition of amines to 3,3-disubstituted cyclopropenes". Organic & Biomolecular Chemistry 13, n.º 34 (2015): 8993–95. http://dx.doi.org/10.1039/c5ob01462j.
Texto completo da fonteAlonso, Miguel E., José Daniel Gómez e Sarah V. Pekerar. "Transmission of electronic effects through 2-[donor]-1-[acceptor] cyclopropanes. Part III. Conformational studies of 2-(p-x-aryl)-1-cyclopropane aldehydes with lanthanide shift reagents." Tetrahedron 49, n.º 34 (agosto de 1993): 7427–36. http://dx.doi.org/10.1016/s0040-4020(01)87219-7.
Texto completo da fonteSundaravelu, Nallappan, e Govindasamy Sekar. "Domino Synthesis of Thioflavones and Thioflavothiones by Regioselective Ring Opening of Donor–Acceptor Cyclopropane Using In-Situ-Generated Thiolate Anions". Organic Letters 21, n.º 17 (16 de agosto de 2019): 6648–52. http://dx.doi.org/10.1021/acs.orglett.9b02210.
Texto completo da fonteZheng, Zhong‐Bo, Wen‐Fu Cheng, Lijia Wang, Jun Zhu, Xiu‐Li Sun e Yong Tang. "Asymmetric Catalytic [3+2] Annulation of Donor‐Acceptor Cyclopropane with Cyclic Ketones: Facile Access to Enantioenriched 1‐Oxaspiro [4.5]decanes †". Chinese Journal of Chemistry 38, n.º 12 (6 de outubro de 2020): 1629–34. http://dx.doi.org/10.1002/cjoc.202000277.
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