Статті в журналах з теми "Donor-Acceptor cyclopropane"
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Craig, Alexander J., та Bill C. Hawkins. "The Bonding and Reactivity of α-Carbonyl Cyclopropanes". Synthesis 52, № 01 (1 жовтня 2019): 27–39. http://dx.doi.org/10.1055/s-0039-1690695.
Повний текст джерелаBoichenko, 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, and Olga A. Ivanova. "Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines." Molecules 27, no. 23 (December 2, 2022): 8468. http://dx.doi.org/10.3390/molecules27238468.
Повний текст джерелаMead, Keith, and Yahaira Reyes. "Acetoxy-Substituted Cyclopropane Dicarbonyls as Stable Donor–Acceptor–Acceptor Cyclopropanes." Synthesis 47, no. 19 (June 25, 2015): 3020–26. http://dx.doi.org/10.1055/s-0034-1379934.
Повний текст джерелаFadeev, Alexander A., Alexey O. Chagarovskiy, Anton S. Makarov, Irina I. Levina, Olga A. Ivanova, Maxim G. Uchuskin, and Igor V. Trushkov. "Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones." Molecules 25, no. 23 (December 5, 2020): 5748. http://dx.doi.org/10.3390/molecules25235748.
Повний текст джерелаGrover, Huck K., Michael R. Emmett, and Michael A. Kerr. "Carbocycles from donor–acceptor cyclopropanes." Organic & Biomolecular Chemistry 13, no. 3 (2015): 655–71. http://dx.doi.org/10.1039/c4ob02117g.
Повний текст джерелаReyes, Yahaira, and Keith T. Mead. "ChemInform Abstract: Acetoxy-Substituted Cyclopropane Dicarbonyls as Stable Donor-Acceptor-Acceptor Cyclopropanes." ChemInform 47, no. 7 (January 2016): no. http://dx.doi.org/10.1002/chin.201607087.
Повний текст джерелаBudynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin, and Mikhail Melnikov. "Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles." Synthesis 49, no. 14 (May 18, 2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.
Повний текст джерелаIvanova, Olga, Vladimir Andronov, Irina Levina, Alexey Chagarovskiy, Leonid Voskressensky, and Igor Trushkov. "Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates." Molecules 24, no. 1 (December 24, 2018): 57. http://dx.doi.org/10.3390/molecules24010057.
Повний текст джерелаLiu, Haidong, Lifang Tian, Hui Wang, Zhi-Qiang Li, Chi Zhang, Fei Xue, and Chao Feng. "A novel type of donor–acceptor cyclopropane with fluorine as the donor: (3 + 2)-cycloadditions with carbonyls." Chemical Science 13, no. 9 (2022): 2686–91. http://dx.doi.org/10.1039/d2sc00302c.
Повний текст джерелаCavitt, Marchello A., Lien H. Phun, and Stefan France. "Intramolecular donor–acceptor cyclopropane ring-opening cyclizations." Chem. Soc. Rev. 43, no. 3 (2014): 804–18. http://dx.doi.org/10.1039/c3cs60238a.
Повний текст джерелаIvanova, Olga A., Vitaly V. Shorokhov, Ivan A. Andreev, Nina K. Ratmanova, Victor B. Rybakov, Elena D. Strel’tsova, and Igor V. Trushkov. "Synthesis of 2-[2-(Ethoxymethoxy)phenyl]spiro[cyclopropane-1,2′-indene]-1′,3′-dione." Molbank 2023, no. 1 (March 14, 2023): M1604. http://dx.doi.org/10.3390/m1604.
Повний текст джерелаMlostoń, Grzegorz, Mateusz Kowalczyk, André U. Augustin, Peter G. Jones, and 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 (June 10, 2020): 1288–95. http://dx.doi.org/10.3762/bjoc.16.109.
Повний текст джерелаHayakawa, Kosuke, Shin-ichi Matsuoka, and Masato Suzuki. "Ring-opening polymerization of donor–acceptor cyclopropanes catalyzed by Lewis acids." Polymer Chemistry 8, no. 25 (2017): 3841–47. http://dx.doi.org/10.1039/c7py00794a.
Повний текст джерелаAugustin, André U., and Daniel B. Werz. "Exploiting Heavier Organochalcogen Compounds in Donor–Acceptor Cyclopropane Chemistry." Accounts of Chemical Research 54, no. 6 (March 4, 2021): 1528–41. http://dx.doi.org/10.1021/acs.accounts.1c00023.
Повний текст джерелаCavitt, Marchello A., Lien H. Phun, and Stefan France. "ChemInform Abstract: Intramolecular Donor-Acceptor Cyclopropane Ring-Opening Cyclizations." ChemInform 45, no. 17 (April 10, 2014): no. http://dx.doi.org/10.1002/chin.201417267.
Повний текст джерелаKreft, Alexander, Peter G. Jones, and Daniel B. Werz. "The Cyclopropyl Group as a Neglected Donor in Donor–Acceptor Cyclopropane Chemistry." Organic Letters 20, no. 7 (March 20, 2018): 2059–62. http://dx.doi.org/10.1021/acs.orglett.8b00603.
Повний текст джерелаSliwinska, Anna, Wojciech Czardybon, and John Warkentin. "Zwitterion from a Cyclopropane with Geminal Donor and Acceptor Groups." Organic Letters 9, no. 4 (February 2007): 695–98. http://dx.doi.org/10.1021/ol063021s.
Повний текст джерелаAlonso, Miguel E., Sarah V. Pekerar, and Maria L. Borgo. "Transmission of electronic effects through 2-[donor]-1-[acceptor]-cyclopropane." Magnetic Resonance in Chemistry 28, no. 11 (November 1990): 956–62. http://dx.doi.org/10.1002/mrc.1260281110.
Повний текст джерелаCruz-Cabeza, Aurora J., та 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, № 2 (25 лютого 2012): 182–88. http://dx.doi.org/10.1107/s0108768111054991.
Повний текст джерелаAllen, F. H., J. P. M. Lommerse, V. J. Hoy, J. A. K. Howard та G. R. Desiraju. "The hydrogen-bond C–H donor and π-acceptor characteristics of three-membered rings". Acta Crystallographica Section B Structural Science 52, № 4 (1 серпня 1996): 734–45. http://dx.doi.org/10.1107/s0108768196005319.
Повний текст джерелаReissig, Hans-Ulrich, and Reinhold Zimmer. "Donor−Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis†." Chemical Reviews 103, no. 4 (April 2003): 1151–96. http://dx.doi.org/10.1021/cr010016n.
Повний текст джерелаBeyzavi, M. Hassan, Carolin Nietzold, Hans-Ulrich Reissig, and Arno Wiehe. "Synthesis of Functionalizedtrans-A2B2-Porphyrins Using Donor-Acceptor Cyclopropane-Derived Dipyrromethanes." Advanced Synthesis & Catalysis 355, no. 7 (April 30, 2013): 1409–22. http://dx.doi.org/10.1002/adsc.201300141.
Повний текст джерелаZhang, Yanqun, Manyu Jin, Cunqi Wu, Yongxia Zhao, Hua Zhou, and Jingwei Xu. "A practical and reusable catalyst for the synthesis of donor-acceptor cyclopropane." Catalysis Communications 103 (January 2018): 5–9. http://dx.doi.org/10.1016/j.catcom.2017.09.009.
Повний текст джерелаLevitskiy, Oleg A., Olga I. Aglamazova, Yuri K. Grishin, and 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 (September 8, 2022): 1166–76. http://dx.doi.org/10.3762/bjoc.18.121.
Повний текст джерелаMorales, Christian L., and Brian L. Pagenkopf. "Total Synthesis of (±)-Goniomitine via a Formal Nitrile/Donor−Acceptor Cyclopropane [3 + 2] Cyclization." Organic Letters 10, no. 2 (January 2008): 157–59. http://dx.doi.org/10.1021/ol702376j.
Повний текст джерелаZheng, Xiaomei, and Michael A. Kerr. "Synthesis and Cross-Coupling Reactions of 7-Azaindoles via a New Donor−Acceptor Cyclopropane." Organic Letters 8, no. 17 (August 2006): 3777–79. http://dx.doi.org/10.1021/ol061379i.
Повний текст джерелаBrand, Christian, Gesche Rauch, Michele Zanoni, Birger Dittrich, and Daniel B. Werz. "Synthesis of [n,5]-Spiroketals by Ring Enlargement of Donor-Acceptor-Substituted Cyclopropane Derivatives." Journal of Organic Chemistry 74, no. 22 (November 20, 2009): 8779–86. http://dx.doi.org/10.1021/jo901902g.
Повний текст джерелаBeyzavi, M. Hassan, Carolin Nietzold, Hans-Ulrich Reissig, and Arno Wiehe. "ChemInform Abstract: Synthesis of Functionalized trans-A2B2-Porphyrins Using Donor-Acceptor Cyclopropane-Derived Dipyrromethanes." ChemInform 44, no. 38 (August 30, 2013): no. http://dx.doi.org/10.1002/chin.201338109.
Повний текст джерелаSabbatani, Juliette, and Nuno Maulide. "Temporary Generation of a Cyclopropyl Oxocarbenium Ion Enables Highly Diastereoselective Donor-Acceptor Cyclopropane Cycloaddition." Angewandte Chemie International Edition 55, no. 23 (April 21, 2016): 6780–83. http://dx.doi.org/10.1002/anie.201601340.
Повний текст джерелаKang, Qikai, Lijia Wang, Zhongbo Zheng, Junfang Li, and Yong Tang. "Sidearm as a Control in the Asymmetric Ring Opening Reaction of Donor-Acceptor Cyclopropane." Chinese Journal of Chemistry 32, no. 8 (April 4, 2014): 669–72. http://dx.doi.org/10.1002/cjoc.201400053.
Повний текст джерелаLund, Elizabeth A., Isaac A. Kennedy та Alex G. Fallis. "Dihydrofurans from α-diazoketones due to facile ring opening – cyclization of donor–acceptor cyclopropane intermediates". Canadian Journal of Chemistry 74, № 12 (1 грудня 1996): 2401–12. http://dx.doi.org/10.1139/v96-269.
Повний текст джерелаPilsl, Ludwig K. A., Thomas Ertl та Oliver Reiser. "Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor–Acceptor Cyclopropane as Key Intermediate". Organic Letters 19, № 10 (9 травня 2017): 2754–57. http://dx.doi.org/10.1021/acs.orglett.7b01111.
Повний текст джерелаGharpure, Santosh J., Laxmi Narayan Nanda, and Dimple Kumari. "Enantiospecific Total Synthesis of (+)-3-epi -Epohelmin A Using a Nitrogen-Substituted Donor-Acceptor Cyclopropane." European Journal of Organic Chemistry 2017, no. 27 (July 18, 2017): 3917–20. http://dx.doi.org/10.1002/ejoc.201700498.
Повний текст джерелаAlford, Joshua S., та 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, № 23 (15 листопада 2012): 6020–23. http://dx.doi.org/10.1021/ol3029127.
Повний текст джерелаGharpure, Santosh J., Laxmi Narayan Nanda, and Manoj Kumar Shukla. "Donor–Acceptor Substituted Cyclopropane to Butanolide and Butenolide Natural Products: Enantiospecific First Total Synthesis of (+)-Hydroxyancepsenolide." Organic Letters 16, no. 24 (December 8, 2014): 6424–27. http://dx.doi.org/10.1021/ol503246k.
Повний текст джерелаNovikov, Roman A., Anna V. Tarasova, Victor A. Korolev, Vladimir P. Timofeev, and Yury V. Tomilov. "A New Type of Donor-Acceptor Cyclopropane Reactivity: The Generation of Formal 1,2- and 1,4-Dipoles." Angewandte Chemie 126, no. 12 (February 19, 2014): 3251–55. http://dx.doi.org/10.1002/ange.201306186.
Повний текст джерелаKang, Qikai, Lijia Wang, Zhongbo Zheng, Junfang Li, and Yong Tang. "ChemInform Abstract: Sidearm as a Control in the Asymmetric Ring Opening Reaction of Donor-Acceptor Cyclopropane." ChemInform 46, no. 8 (February 2015): no. http://dx.doi.org/10.1002/chin.201508033.
Повний текст джерелаNovikov, Roman A., Anna V. Tarasova, Victor A. Korolev, Vladimir P. Timofeev, and 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, no. 12 (February 19, 2014): 3187–91. http://dx.doi.org/10.1002/anie.201306186.
Повний текст джерелаAlonso, Miguel E., and 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, no. 6 (June 1991): 587–93. http://dx.doi.org/10.1002/mrc.1260290609.
Повний текст джерелаXiao, Jun-An, Jie Li, Peng-Ju Xia, Zhao-Fang Zhou, Zhao-Xu Deng, Hao-Yue Xiang, Xiao-Qing Chen, and 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, no. 22 (November 3, 2016): 11185–94. http://dx.doi.org/10.1021/acs.joc.6b02172.
Повний текст джерелаLUND, E. A., I. A. KENNEDY та A. G. FALLIS. "ChemInform Abstract: Dihydrofurans from α-Diazoketones Due to Facile Ring Opening - Cyclization of Donor-Acceptor Cyclopropane Intermediates." ChemInform 28, № 27 (3 серпня 2010): no. http://dx.doi.org/10.1002/chin.199727124.
Повний текст джерелаAlford, Joshua S., та 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, № 19 (18 квітня 2013): no. http://dx.doi.org/10.1002/chin.201319048.
Повний текст джерелаGhosh, Asit, Subhajit Mandal, Pratim Kumar Chattaraj, and Prabal Banerjee. "Ring Expansion of Donor–Acceptor Cyclopropane via Substituent Controlled Selective N-Transfer of Oxaziridine: Synthetic and Mechanistic Insights." Organic Letters 18, no. 19 (September 29, 2016): 4940–43. http://dx.doi.org/10.1021/acs.orglett.6b02417.
Повний текст джерелаNovikov, Roman A., Anna V. Tarasova, Victor A. Korolev, Vladimir P. Timofeev, and 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, no. 36 (August 21, 2014): no. http://dx.doi.org/10.1002/chin.201436034.
Повний текст джерелаVartanova, Anna E., Irina I. Levina, Victor B. Rybakov, Olga A. Ivanova, and 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, no. 17 (August 12, 2021): 12300–12308. http://dx.doi.org/10.1021/acs.joc.1c01064.
Повний текст джерелаYang, Hua, Jie Li, Jun-An Xiao, Shu-Juan Zhao, and 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, no. 18 (July 19, 2017): 4292–98. http://dx.doi.org/10.1055/s-0036-1588876.
Повний текст джерелаMaslivetc, Vladimir A., Marina Rubina, and Michael Rubin. "One-pot synthesis of GABA amides via the nucleophilic addition of amines to 3,3-disubstituted cyclopropenes." Organic & Biomolecular Chemistry 13, no. 34 (2015): 8993–95. http://dx.doi.org/10.1039/c5ob01462j.
Повний текст джерелаAlonso, Miguel E., José Daniel Gómez, and 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, no. 34 (August 1993): 7427–36. http://dx.doi.org/10.1016/s0040-4020(01)87219-7.
Повний текст джерелаSundaravelu, Nallappan, and 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, no. 17 (August 16, 2019): 6648–52. http://dx.doi.org/10.1021/acs.orglett.9b02210.
Повний текст джерелаZheng, Zhong‐Bo, Wen‐Fu Cheng, Lijia Wang, Jun Zhu, Xiu‐Li Sun, and 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, no. 12 (October 6, 2020): 1629–34. http://dx.doi.org/10.1002/cjoc.202000277.
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