Cite the Following Article
Stereo- and regioselectivity of the hetero-Diels–Alder reaction of nitroso derivatives with conjugated dienes
Lucie Brulíková, Aidan Harrison, Marvin J. Miller and Jan Hlaváč
Beilstein J. Org. Chem. 2016, 12, 1949–1980.
https://doi.org/10.3762/bjoc.12.184
How to Cite
Brulíková, L.; Harrison, A.; Miller, M. J.; Hlaváč, J. Beilstein J. Org. Chem. 2016, 12, 1949–1980. doi:10.3762/bjoc.12.184
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: 113.0 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Jia, L.; Liu, H.; Shi, W.; Xu, Y.; Sun, R.; Zuo, J.; Wang, B.; Huang, J.; Zhong, F.; Wang, D. A bifunctional recyclable Gemini surfactant catalyst for oxidative nitroso Diels–Alder reactions in water. Green Chemistry 2025, 27, 13885–13892. doi:10.1039/d5gc03912f
- Zhu, M.; Liu, L.; Zhi, Y.; Hou, H. Visible-light mediated oxidative Diels-Alder reaction of hydroxylamines and 1,3-dienes. Tetrahedron 2025, 184, 134752. doi:10.1016/j.tet.2025.134752
- Yu, L.; Diaz, J.; Kroeger, A. A.; Coote, M. L.; Chan, P. W. H. Chiral Brønsted Acid-Catalyzed Regio-, Diastereo-, and Enantioselective Formal [2 + 2 + 2] Cycloaddition of 3-Vinyl-1H-indoles with Nitrosobenzenes. ACS Catalysis 2024, 14, 13269–13282. doi:10.1021/acscatal.3c05041
- Pairas, G. N.; Tsoungas, P. G. Highlighting the Underrated Side of the High Profile Nitroso Entity as a Nucleophile. ChemistrySelect 2023, 8. doi:10.1002/slct.202302671
- Fouad, M. A.; Ferretti, F.; Galiè, S.; Ragaini, F. Use of Formic Acid as a CO Surrogate for the Reduction of Nitroarenes in the Presence of Dienes: A Two‐Step Synthesis of N‐Arylpyrroles via 1,2‐Oxazines. European Journal of Organic Chemistry 2023, 26. doi:10.1002/ejoc.202300809
- Antonova, Y. A.; Nelyubina, Y. V.; Ioffe, S. L.; Tabolin, A. A. [3+3]-Annulation of Cyclic Nitronates with Vinyl Diazoacetates: Diastereoselective Synthesis of Partially Saturated [1,2]Oxazino[2,3-b][1,2]oxazines and Their Base-Promoted Ring Contraction to Pyrrolo[1,2-b][1,2]oxazine Derivatives. Molecules (Basel, Switzerland) 2023, 28, 3025. doi:10.3390/molecules28073025
- Hamzehloueian, M.; Haghdadi, M.; Lotfi, M. A Theoretical Evaluation of the Behavior of Nitrosoamidine upon Reacting with Methoxy Butadiene as Potential Heterodiene or Heterodienophile. Letters in Organic Chemistry 2022, 19, 857–866. doi:10.2174/1570178619666220113113638
- Yu, L.; Li, W.; Tapdara, A.; Kyne, S. H.; Harode, M.; Babaahmadi, R.; Ariafard, A.; Chan, P. W. H. Chiral Gold Complex Catalyzed Cycloisomerization/Regio- and Enantioselective Nitroso-Diels–Alder Reaction of 1,6-Diyne Esters with Nitrosobenzenes. ACS Catalysis 2022, 12, 7288–7299. doi:10.1021/acscatal.2c01680
- Majireck, M. M.; Bennett, J. M. Comprehensive Heterocyclic Chemistry IV - 1,2-Oxazines and Their Benzo Derivatives. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 283–415. doi:10.1016/b978-0-12-818655-8.00013-5
- Bianchi, P.; Monbaliu, J.-C. Three decades of unveiling the complex chemistry of C-nitroso species with computational chemistry. Organic Chemistry Frontiers 2021, 9, 223–264. doi:10.1039/d1qo01415c
- Hadavi, D.; Han, P.; Honing, M. Ion mobility spectrometry-tandem mass spectrometry strategies for the on-line monitoring of a continuous microflow reaction. Journal of Flow Chemistry 2021, 12, 175–184. doi:10.1007/s41981-021-00209-7
- Zhao, F.; Yu, P.; Chen, Y.; Liu, F.; Houk, K. N. π-Facial Stereoselectivity in Acyl Nitroso Cycloadditions to 5,5-Unsymmetrically Substituted Cyclopentadienes: Computational Exploration of Origins of Selectivity and the Role of Substituent Conformations on Selectivity. The Journal of organic chemistry 2021, 86, 17082–17089. doi:10.1021/acs.joc.1c02191
- Hilt, G.; Hermann, L.; Fährmann, J. The Application of 1,2-Oxazinanes as Chiral Cyclic Weinreb Amide-type Auxiliaries Leading to a Three Component One-Pot Reaction. Synthesis 2021, 54, 2005–2018. doi:10.1055/a-1683-0484
- Ticli, V.; Zhao, Z.; Du, L.; Kornienko, A.; Hudlicky, T. Synthesis and biological evaluation of 10-benzyloxy-Narciclasine. Tetrahedron 2021, 101, 132505. doi:10.1016/j.tet.2021.132505
- Zhai, L.; Tang, Y.; Zhang, Y.; Huang, S.-H.; Zhu, L.; Hong, R. A Bridge to Alkaloid Synthesis. Chemical record (New York, N.Y.) 2021, 22, e202100197. doi:10.1002/tcr.202100197
- Hilt, G.; Fährmann, J. Alternating Current Electrolysis as Efficient Tool for the Direct Electrochemical Oxidation of Hydroxamic Acids for Acyl Nitroso Diels-Alder Reactions. Angewandte Chemie (International ed. in English) 2021, 60, 20313–20317. doi:10.1002/anie.202107148
- Fährmann, J.; Hilt, G. Wechselstromelektrolyse als effizientes Instrument für die direkte elektrochemische Oxidation von Hydroxamsäuren für die Acyl‐Nitroso Diels‐Alder‐Reaktion. Angewandte Chemie 2021, 133, 20476–20480. doi:10.1002/ange.202107148
- Han, J.; Jiang, L.; Zhang, L.; Quinn, R. J.; Liu, X.; Feng, Y. Peculiarities of meroterpenoids and their bioproduction. Applied microbiology and biotechnology 2021, 105, 3987–4003. doi:10.1007/s00253-021-11312-z
- Kassin, V.-E.; Morodo, R.; Toupy, T.; Jacquemin, I.; Van Hecke, K.; Robiette, R.; Monbaliu, J.-C. A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones. Green Chemistry 2021, 23, 2336–2351. doi:10.1039/d0gc04395h
- Wang, D.; Song, Z.; Zhang, J.; Xu, T. Remote methylene C(sp3)–H functionalization enabled by organophosphine-catalyzed alkyne isomerization. Organic Chemistry Frontiers 2021, 8, 1125–1131. doi:10.1039/d0qo01399d