Cite the Following Article
Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective
Yaroslav D. Boyko, Valentin S. Dorokhov, Alexey Yu. Sukhorukov and Sema L. Ioffe
Beilstein J. Org. Chem. 2017, 13, 2214–2234.
https://doi.org/10.3762/bjoc.13.220
How to Cite
Boyko, Y. D.; Dorokhov, V. S.; Sukhorukov, A. Y.; Ioffe, S. L. Beilstein J. Org. Chem. 2017, 13, 2214–2234. doi:10.3762/bjoc.13.220
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
Picture with graphical abstract, title and authors for social media postings and presentations. | ||
Format: PNG | Size: 133.5 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Pospelov, E. V.; Sukhorukov, A. Y. Building Up a Piperazine Ring from a Primary Amino Group via Catalytic Reductive Cyclization of Dioximes. International journal of molecular sciences 2023, 24, 11794. doi:10.3390/ijms241411794
- Wang, T.; Liu, C.; Xu, D.; Xu, J.; Yang, Z. Iridium-Catalyzed and pH-Dependent Reductions of Nitroalkenes to Ketones. Molecules (Basel, Switzerland) 2022, 27, 7822. doi:10.3390/molecules27227822
- Schuppe, A. W.; Liu, Y.; Gonzalez-Hurtado, E.; Zhao, Y.; Jiang, X.; Ibarraran, S.; Huang, D.; Wang, E.; Lee, J.; Loria, J. P.; Dixit, V. D.; Li, X.; Newhouse, T. R. Unified Total Synthesis of the Limonoid Alkaloids: Strategies for the De Novo Synthesis of Highly Substituted Pyridine Scaffolds. Chem 2022, 8, 2856–2887. doi:10.1016/j.chempr.2022.09.012
- Pospelov, E. V.; Boyko, Y. D.; Ioffe, S. L.; Sukhorukov, A. Y. Synthesis of Bis(β‐Oximinoalkyl)malonates and Their Catalytic Reductive Cyclization to Piperidines. Advanced Synthesis & Catalysis 2022, 364, 2557–2564. doi:10.1002/adsc.202200424
- Mamatha Jyothi, R. S.; Sripathi, M. P.; Thirupathi, P. Recent Advances in Base-assisted Michael Addition Reactions. Current Organic Chemistry 2022, 26, 1264–1293. doi:10.2174/1385272826666220827095110
- Shen, L.-W.; Wang, Z.-H.; You, Y.; Zhao, J.-Q.; Zhou, M.-Q.; Yuan, W.-C. α-Nitrosostyrenes as Three-Atom Units for the (3+1) Cyclization Reaction: Facile Access to 2,3-Dihydrodiazete N-Oxides and Their Diversified Synthetic Conversions. Organic letters 2022, 24, 1094–1099. doi:10.1021/acs.orglett.2c00024
- Schuppe, A. W.; Liu, Y.; Zhao, Y.; Ibarraran, S.; Huang, D.; Wang, E.; Lee, J.; Loria, J. P.; Newhouse, T. Strategies for the De Novo Synthesis of Highly Substituted Pyridine Scaffolds: Unified Total Synthesis of the Limonoid Alkaloids. SSRN Electronic Journal 2022. doi:10.2139/ssrn.4012183
- Akhmirov, R. T.; Ioffe, S. L.; Sukhorukov, A. Y. Stereoselective approach to conjugated enone oximes from aliphatic nitro compounds and sulfur ylides. Mendeleev Communications 2021, 31, 686–689. doi:10.1016/j.mencom.2021.09.031
- Cardoso, A. L.; Lopes, S.; Grosso, C.; Pineiro, M.; Lemos, A.; Pinho e Melo, T. M. V. D. One-Pot Synthetic Approach to Dipyrromethanes and Bis(indolyl)methanes via Nitrosoalkene Chemistry. Journal of Chemical Education 2021, 98, 2661–2666. doi:10.1021/acs.jchemed.1c00184
- Hua, T.-B.; Liu, C.-X.; Weimin, H.; Wang, L.; Yang, Q.-Q. Mild synthesis of isoxazoline derivatives via an efficient [4 + 1] annulation reaction of transient nitrosoalkenes and sulfur ylides. Scientific reports 2021, 11, 2078. doi:10.1038/s41598-021-81370-w
- De, S. K. doi:10.1002/9783527828166.ch4
- Jadhav, P. D.; Chen, J.-X.; Liu, R.-S. Gold(I)-Catalyzed Highly Enantioselective [4 + 2]-Annulations of Cyclopentadienes with Nitrosoarenes via Nitroso-Povarov versus Oxidative Nitroso-Povarov Reactions. ACS Catalysis 2020, 10, 5840–5845. doi:10.1021/acscatal.0c01293
- Ling, T.; Hadi, V.; Bollinger, J. C.; Rivas, F. Identification of rapid access to polycyclic systems via a base-catalyzed cascade cyclization reaction and their biological evaluation. Bioorganic chemistry 2020, 99, 103846. doi:10.1016/j.bioorg.2020.103846
- Curti, C.; Battistini, L.; Sartori, A.; Zanardi, F. New Developments of the Principle of Vinylogy as Applied to π-Extended Enolate-Type Donor Systems. Chemical reviews 2020, 120, 2448–2612. doi:10.1021/acs.chemrev.9b00481
- Sukhorukov, A. Y. Umpolung of Enamines: An Overview on Strategies and Synthons. Synlett 2020, 31, 439–449. doi:10.1055/s-0037-1610741
- Sukhorukov, A. Y. C−H Reactivity of the α‐Position in Nitrones and Nitronates. Advanced Synthesis & Catalysis 2019, 362, 724–754. doi:10.1002/adsc.201900718
- Chen, C.-N.; Liu, R.-S. Gold‐catalyzed [4+2]‐Annulations of Dienes with Nitrosoarenes that Serve as 4‐π‐donors to Enable Nitroso‐Povarov Reactions. Angewandte Chemie 2019, 131, 9936–9940. doi:10.1002/ange.201903615
- Chen, C.-N.; Liu, R.-S. Gold-catalyzed [4+2] Annulations of Dienes with Nitrosoarenes as 4 π Donors: Nitroso-Povarov Reactions. Angewandte Chemie (International ed. in English) 2019, 58, 9831–9835. doi:10.1002/anie.201903615
- Naumovich, Y. A.; Ioffe, S. L.; Sukhorukov, A. Y. Michael Addition of P-Nucleophiles to Conjugated Nitrosoalkenes. The Journal of organic chemistry 2019, 84, 7244–7254. doi:10.1021/acs.joc.9b00924
- Ushakov, P. Y.; Tabolin, A. A.; Ioffe, S. L.; Sukhorukov, A. Y. In Situ Generated Magnesium Cyanide as an Efficient Reagent for Nucleophilic Cyanation of Nitrosoalkenes and Parent Nitronates. European Journal of Organic Chemistry 2019, 2019, 1888–1892. doi:10.1002/ejoc.201801761