SynOpen, Inhaltsverzeichnis CC BY-NC-ND 4.0 · SynOpen 2021; 05(03): 229-231DOI: 10.1055/a-1577-4661 spotlight Synthesis of Nitroolefins via the Direct Nitration of Alkenes Mohamed Hassan a Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663 Kaiserslautern, Germany b Department of Chemistry, Faculty of Science, Aswan University, Aswan 81528, Egypt , Cedric Ndefo Nde a Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663 Kaiserslautern, Germany , Georg Manolikakes ∗ a Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663 Kaiserslautern, Germany› InstitutsangabenArtikel empfehlen Abstract Alle Artikel dieser RubrikKey words Key wordsnitrooelfin - Michael acceptor - synthetic methodology - nitration - alkenes Volltext Referenzen References 1 Barrett AG. M, Graboski GG. Chem. Rev. 1986; 86: 751 2 Ono N. The Nitro Group in Organic Synthesis . Wiley-VCH; New York: 2001 3 Piesche M, Roos J, Kühn B, Fettel J, Hellmuth N, Brat C, Maucher IV, Awad O, Matrone C, Comerma SteffensenS. G, Manolikakes G, Heinicke U, Zacharowski KD, Steinhilber D, Maier T. J. Front. Pharmacol. 2020; 11: 1297 4 Yan G, Borah AJ, Wang L. Org. Biomol. Chem. 2014; 12: 6094 For two recent examples, see: 5a Hassan M, Krieg S.-C, Ndefo Nde C, Roos J, Maier TJ, El Rady EA, Raslan MA, Sadek KU, Manolikakes G. Eur. J. Org. Chem. 2021; 2239 5b Ishitani H, Saito Y, Tsubogo T, Kobayashi S. Org. Lett. 2016; 18: 1346 6 Freeman BA, Baker PR. S, Schopfer FJ, Woodcock SR, Napolitano A, d’Ischia M. J. Chem. Biol. 2008; 283: 15515 7 Tinsley SW. J. Org. Chem. 1961; 26: 4723 8a Maity S, Manna S, Rana S, Naveen T, Mallick A, Maiti D. J. Am. Chem. Soc. 2013; 135: 3355 8b Naveen T, Maity S, Sharma U, Maiti D. J. Org. Chem. 2013; 78: 59545 9 Begari E, Singh C, Nookaraju U, Kumar P. Synlett 2014; 25: 1997 10a Maity S, Naveen T, Sharma U, Maiti D. Org. Lett. 2013; 15: 3384 10b Zhao A, Jiang Q, Jia J, Xu B, Liu Y, Zhang M, Liu Q, Luo W, Guo C. Tetrahedron Lett. 2016; 57: 80 11a Hlekhlai S, Samakkanad N, Sawangphon T, Pohmakotr M, Reutrakul V, Soorukram D, Jaipetch T, Kuhakarn C. Eur. J. Org. Chem. 2014; 7433 11b Ambala S, Singh R, Singh M, Cham PS, Gupta R, Munagala G, Yempalla KR, Vishwakarma RA, Singh PP. RSC Adv. 2019; 9: 30428 12 Mir BA, Singh SJ, Kumar R, Patel BK. Adv. Synth. Catal. 2018; 360: 3801 13 Reddy GS, Corey EJ. Org. Lett. 2021; 23: 3399 14 Casiello M, Caputo D, Fusco C, Cotugno P, Rizzi V, Dell’Anna MM, D’Accolti L, Nacci A. Eur. J. Org. Chem. 2020; 6012 15 Zhang K, Jelier B, Passera A, Jeschke G, Katayev D. Chem. Eur. J. 2019; 25: 12929