How to cite this paper
Łapczuk-Krygier, A & Ponikiewski, . (2015). Single crystal X-ray structure of (Z)-1-bromo-1-nitro-2-phenylethene.Current Chemistry Letters, 4(1), 21-26.
Refrences
1. Łapczuk-Krygier, A., Ponikiewski, Ł., Jasi?ski, R. (2014) The Crystal Structure of (1RS,4RS,5RS,6SR)-5-cyano-5-nitro-6-phenyl-bicyclo[2.2.1]hept-2-ene. Crystallogr. Reports 59, 961–963.
2. Jasiński, R. (2012) Exploration of regiospecificity phenomenon in [2+3] cycloaddition reactions between arylnitrones and trans-substituted nitroethenes on the basis of the reactivity indices theory. Current Chem. Lett. 1, 157–162.
3. R. Jasiński, M. Kubik, A. Łapczuk-Krygier, A. Kącka, E. Dresler, and A. Boguszewska-Czubara (2014) An experimental and theoretical study of the hetero Diels–Alder reactions between (E)-2-aryl-1-cyano-1-nitroethenes and ethyl vinyl ether: one-step or zwitterionic, two-step mechanism? React. Kinet. Mech. Catal.. doi:10.1007/s11144-014-0753-8
4. Parham, W., Bleasdale, J. (1951) The Condensation of Diazo Compounds with Nitroölefins. II. 3-Bromo-and 3-Nitropyrazoles. J. Am. Chem. Soc. 73, 4664–4666.
5. R. Jasiński, M. Mikulska, O. Koifman, and A. Barański (2013) Conjugated nitroalkenes in cycloaddition reactions 18*. Regio- and stereoselectivity of (2+3) cycloaddition reactions between gem-chloronitroethene and (Z)-C,N-diarylnitrones. Chem. Heterocycl. Compd. 49, 1188–1194.
6. A. G. Clark, B. Croshaw, B. E. Leggetter, and D. F. Spooner (1974) “Synthesis and Antimicrobial Activity of Aliphatic Nitro Compounds,” J. Med. Chem., 17, 9, 977–981.
7. Schales, O., Graefe, H. A. (1952) Arylnitroalkenes: A New Group of Antibacterial Agents1. J. Am. Chem. Soc. 74, 4486–4490.
8. N. Milhazes, R. Calheiros, M. P. M. Marques, J. Garrido, M. N. D. S. Cordeiro, C. Rodrigues, S. Quinteira, C. Novais, L. Peixe, and F. Borges (2006) Beta-nitrostyrene derivatives as potential antibacterial agents: a structure-property-activity relationship study. Bioorg. Med. Chem. 14, 4078–4088.
9. P. Cheng, Z.-Y. Jiang, R.-R. Wang, X.-M. Zhang, Q. Wang, Y.-T. Zheng, J. Zhou, and J.-J. Chen (2007) Synthesis and biological evaluation of N-acetyl-beta-aryl-1,2-didehydroethylamines as new HIV-1 RT inhibitors in vitro. Bioorg. Med. Chem. Lett. 17, 4476–4480.
10. S. Kaap, I. Quentin, D. Tamiru, M. Shaheen, K. Eger, and H. J. Steinfelder (2003) Structure activity analysis of the pro-apoptotic, antitumor effect of nitrostyrene adducts and related compounds. Biochem. Pharmacol. 65, 603–610.
11. Kim, J. H. (2003) Potent Inhibition of Human Telomerase by Nitrostyrene Derivatives. Mol. Pharmacol. 63, 1117–1124.
12. Jasiński, R., Koifman, O., Barański, A. (2011) A B3LYP/6-31G(d) study of Diels-Alder reactions between cyclopentadiene and (E)-2-arylnitroethenes. Cent. Eur. J. Chem. 9, 1008–1018.
13. Jasi?ski, R., Kwiatkowska, M., Bara?ski, A. (2011) Stereoselectivity and kinetics of [4 + 2] cycloaddition reaction of cyclopentadiene to para-substituted E-2-arylnitroethenes. J. Phys. Org. Chem. 24, 843–853.
14. M. Zhang, P. Hu, J. Zhou, G. Wu, S. Huang, and W. Su (2013) Pd-catalyzed multidehydrogenative cross-coupling between (hetero)arenes and nitroethane to construct B-aryl nitroethylenes. Org. Lett. 15, 1718–1721.
15. Bláha, I., Lešetický, L. (1986) Preparation and Z-E isomerization of substituted nitrostyrenes. Collect. Czechoslov. Chem. Commun. 51, 1094–1099.
16. Program CRYSALISPRO Version 1.171 (2008) Oxford Diffraction, Abingdon, England.
17. Sheldrick, G. M. (2008) A short history of SHELX. Acta Crystallogr. A. 64, 112–122.
18. L. A. Chetkina, E. G. Popova, and G. A. Gol’der (1975) “X-ray diffraction investigation of p-dimethylamino-B,B-bromonitrostyrene,” J. Struct. Chem., 15, 5, 768–771.
19. Vogel, A. I. (1956) A textbook of practical organic chemistry, 3rd Ed., Longman, London.
20. Ganesh, M., Namboothiri, I. N. N. (2007) Stereospecific approach to α,β-disubstituted nitroalkenes via coupling of α-bromonitroalkenes with boronic acids and terminal acetylenes. Tetrahedron 63, 11973–11983.
2. Jasiński, R. (2012) Exploration of regiospecificity phenomenon in [2+3] cycloaddition reactions between arylnitrones and trans-substituted nitroethenes on the basis of the reactivity indices theory. Current Chem. Lett. 1, 157–162.
3. R. Jasiński, M. Kubik, A. Łapczuk-Krygier, A. Kącka, E. Dresler, and A. Boguszewska-Czubara (2014) An experimental and theoretical study of the hetero Diels–Alder reactions between (E)-2-aryl-1-cyano-1-nitroethenes and ethyl vinyl ether: one-step or zwitterionic, two-step mechanism? React. Kinet. Mech. Catal.. doi:10.1007/s11144-014-0753-8
4. Parham, W., Bleasdale, J. (1951) The Condensation of Diazo Compounds with Nitroölefins. II. 3-Bromo-and 3-Nitropyrazoles. J. Am. Chem. Soc. 73, 4664–4666.
5. R. Jasiński, M. Mikulska, O. Koifman, and A. Barański (2013) Conjugated nitroalkenes in cycloaddition reactions 18*. Regio- and stereoselectivity of (2+3) cycloaddition reactions between gem-chloronitroethene and (Z)-C,N-diarylnitrones. Chem. Heterocycl. Compd. 49, 1188–1194.
6. A. G. Clark, B. Croshaw, B. E. Leggetter, and D. F. Spooner (1974) “Synthesis and Antimicrobial Activity of Aliphatic Nitro Compounds,” J. Med. Chem., 17, 9, 977–981.
7. Schales, O., Graefe, H. A. (1952) Arylnitroalkenes: A New Group of Antibacterial Agents1. J. Am. Chem. Soc. 74, 4486–4490.
8. N. Milhazes, R. Calheiros, M. P. M. Marques, J. Garrido, M. N. D. S. Cordeiro, C. Rodrigues, S. Quinteira, C. Novais, L. Peixe, and F. Borges (2006) Beta-nitrostyrene derivatives as potential antibacterial agents: a structure-property-activity relationship study. Bioorg. Med. Chem. 14, 4078–4088.
9. P. Cheng, Z.-Y. Jiang, R.-R. Wang, X.-M. Zhang, Q. Wang, Y.-T. Zheng, J. Zhou, and J.-J. Chen (2007) Synthesis and biological evaluation of N-acetyl-beta-aryl-1,2-didehydroethylamines as new HIV-1 RT inhibitors in vitro. Bioorg. Med. Chem. Lett. 17, 4476–4480.
10. S. Kaap, I. Quentin, D. Tamiru, M. Shaheen, K. Eger, and H. J. Steinfelder (2003) Structure activity analysis of the pro-apoptotic, antitumor effect of nitrostyrene adducts and related compounds. Biochem. Pharmacol. 65, 603–610.
11. Kim, J. H. (2003) Potent Inhibition of Human Telomerase by Nitrostyrene Derivatives. Mol. Pharmacol. 63, 1117–1124.
12. Jasiński, R., Koifman, O., Barański, A. (2011) A B3LYP/6-31G(d) study of Diels-Alder reactions between cyclopentadiene and (E)-2-arylnitroethenes. Cent. Eur. J. Chem. 9, 1008–1018.
13. Jasi?ski, R., Kwiatkowska, M., Bara?ski, A. (2011) Stereoselectivity and kinetics of [4 + 2] cycloaddition reaction of cyclopentadiene to para-substituted E-2-arylnitroethenes. J. Phys. Org. Chem. 24, 843–853.
14. M. Zhang, P. Hu, J. Zhou, G. Wu, S. Huang, and W. Su (2013) Pd-catalyzed multidehydrogenative cross-coupling between (hetero)arenes and nitroethane to construct B-aryl nitroethylenes. Org. Lett. 15, 1718–1721.
15. Bláha, I., Lešetický, L. (1986) Preparation and Z-E isomerization of substituted nitrostyrenes. Collect. Czechoslov. Chem. Commun. 51, 1094–1099.
16. Program CRYSALISPRO Version 1.171 (2008) Oxford Diffraction, Abingdon, England.
17. Sheldrick, G. M. (2008) A short history of SHELX. Acta Crystallogr. A. 64, 112–122.
18. L. A. Chetkina, E. G. Popova, and G. A. Gol’der (1975) “X-ray diffraction investigation of p-dimethylamino-B,B-bromonitrostyrene,” J. Struct. Chem., 15, 5, 768–771.
19. Vogel, A. I. (1956) A textbook of practical organic chemistry, 3rd Ed., Longman, London.
20. Ganesh, M., Namboothiri, I. N. N. (2007) Stereospecific approach to α,β-disubstituted nitroalkenes via coupling of α-bromonitroalkenes with boronic acids and terminal acetylenes. Tetrahedron 63, 11973–11983.