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Keybot 114 Results  doktori.bme.hu  Page 5
  Könczöl Là¡szlà³  
[3] a) G. H. Spikes, J. C. Fettinger, P. P. Power, J. Am. Chem. Soc. 2005, 127, 12232–12233. b) Y. Peng, M. Brynda, B. D. Ellis, J. C. Fettinger, E. Rivard, P. P. Power Chem. Commun. 2008, 6042–6044. c) Y. Peng, B. D. Ellis, X. Wang, P. P. Power, J. Am.
[3] a) G. H. Spikes, J. C. Fettinger, P. P. Power, J. Am. Chem. Soc. 2005, 127, 12232–12233. b) Y. Peng, M. Brynda, B. D. Ellis, J. C. Fettinger, E. Rivard, P. P. Power Chem. Commun. 2008, 6042–6044. c) Y. Peng, B. D. Ellis, X. Wang, P. P. Power, J. Am. Chem. Soc. 2008, 130, 12268–12269. d) Y. Peng, J.-D. Guo, B. D. Ellis, Z. Zhu, J. C. Fettinger, S. Nagase, P. P. Power, J. Am. Chem. Soc. 2009, 131, 16272–16282. e) Z. Zhu, X. Wang, Y. Peng, H. Lei, J. C. Fettinger, E. Rivard, P. P. Power, Angew. Chem. 2009, 121, 2065–2068; Angew. Chem. Int. Ed. 2009, 48, 2031–2034.
  Könczöl Là¡szlà³  
[6] D. W. Stephan, G. Erker, Angew. Chem. 2010, 122, 50–81; Angew. Chem. Int. Ed. 2010, 49, 46–76
[6] D. W. Stephan, G. Erker, Angew. Chem. 2010, 122, 50–81; Angew. Chem. Int. Ed. 2010, 49, 46–76.
  Könczöl Là¡szlà³  
[6] D. W. Stephan, G. Erker, Angew. Chem. 2010, 122, 50–81; Angew. Chem. Int. Ed. 2010, 49, 46–76
[6] D. W. Stephan, G. Erker, Angew. Chem. 2010, 122, 50–81; Angew. Chem. Int. Ed. 2010, 49, 46–76.
  Vass Mà¡rton  
Tarcsay, Á. , Paragi, G., Vass, M., Jójárt, B., Bogár, F., Keserű, G. M. : The impact of molecular dynamics sampling on the performance of virtual screening against GPCRs. J. Chem. Inf. Model. , 2013, 53, pp. 2990-2999 (IF: 4.304)
T1. Tarcsay, Á., Paragi, G., Vass, M., Jójárt, B., Bogár, F., Keserű, G.M. The impact of molecular dynamics sampling on the performance of virtual screening against GPCRs. J. Chem. Inf. Model. 2013, 53, 2990-2999. (IF: 4.304)
  Könczöl Là¡szlà³  
[12] S. Bontemps, G. Bouhadir, P. W. Dyer, K. Miqueu, D. Bourissou, Inorg. Chem. 2007, 46, 5149–5151
[12] S. Bontemps, G. Bouhadir, P. W. Dyer, K. Miqueu, D. Bourissou, Inorg. Chem. 2007, 46, 5149–5151.
  Könczöl Là¡szlà³  
[9] a) T. A. Rokob, A. Hamza, A. Stirling, T. Soós, I. Papai, Angew. Chem. 2008, 120, 2469–2472; Angew. Chem. Int. Ed. 2008, 47, 2435–2438. b) R. Rajeev, R. B. Sunoj, Chem. Eur. J. 2009, 15, 12846–12855.
[9] a) T. A. Rokob, A. Hamza, A. Stirling, T. Soós, I. Papai, Angew. Chem. 2008, 120, 2469–2472; Angew. Chem. Int. Ed. 2008, 47, 2435–2438. b) R. Rajeev, R. B. Sunoj, Chem. Eur. J. 2009, 15, 12846–12855. c) S. Grimme, H. Kruse, L. Goerigk, G. Erker, Angew. Chem. 2010, 122, 1444–1447; Angew. Chem. Int. Ed. 2010, 49, 1402–1405.
  Könczöl Là¡szlà³  
[2] a) A. L. Kenward, W. E. Piers, Angew. Chem. 2008, 120, 38–42; Angew. Chem. Int. Ed. 2008, 47, 38–41. b) D. W. Stephan, Chem. Commun. 2010, 46, 8526–8533. c) P. P. Power, Nature 2010, 463, 171–177.
[2] a) A. L. Kenward, W. E. Piers, Angew. Chem. 2008, 120, 38–42; Angew. Chem. Int. Ed. 2008, 47, 38–41. b) D. W. Stephan, Chem. Commun. 2010, 46, 8526–8533. c) P. P. Power, Nature 2010, 463, 171–177. d) P. P. Power, Acc. Chem. Res. 2011, 44, 627–637.
  Vass Mà¡rton  
7. Chen, D., Ranganathan, A. et al.: Complementarity between in silico and biophysical screening approaches in fragment-based lead discovery against the A2A adenosine receptor, J. Chem. Inf. Model, 2013, 53, 2701
7. Chen, D., Ranganathan, A. et al. Complementarity between in silico and biophysical screening approaches in fragment-based lead discovery against the A2A adenosine receptor. J. Chem. Inf. Model. 2013, 53, 2701.
  Könczöl Là¡szlà³  
[9] a) T. A. Rokob, A. Hamza, A. Stirling, T. Soós, I. Papai, Angew. Chem. 2008, 120, 2469–2472; Angew. Chem. Int. Ed. 2008, 47, 2435–2438. b) R. Rajeev, R. B. Sunoj, Chem. Eur. J. 2009, 15, 12846–12855.
[9] a) T. A. Rokob, A. Hamza, A. Stirling, T. Soós, I. Papai, Angew. Chem. 2008, 120, 2469–2472; Angew. Chem. Int. Ed. 2008, 47, 2435–2438. b) R. Rajeev, R. B. Sunoj, Chem. Eur. J. 2009, 15, 12846–12855. c) S. Grimme, H. Kruse, L. Goerigk, G. Erker, Angew. Chem. 2010, 122, 1444–1447; Angew. Chem. Int. Ed. 2010, 49, 1402–1405.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  MEZEI Pà¡l Dà¡niel  
[O6] Mezei, P. D.; Csonka, G. I. Struct. Chem. 2015, 26, 1367–1379. (IF = 1.837)
[S6] Mezei, P. D.; Csonka, G. I. Struct. Chem. 2015, 26, 1367-1379. (IF = 1,837)
  MEZEI Pà¡l Dà¡niel  
[O7] Mezei, P. D.; Csonka, G. I. Struct. Chem. 2016, STUC-D-16-00037R1 (accepted).
[S7] Mezei, P. D.; Csonka, G. I. Struct. Chem. 2016, STUC-D-16-00037R1 (elfogadva).
  MEZEI Pà¡l Dà¡niel  
[O8] Mezei, P. D.; Ruzsinszky, A.; Csonka, G. I. J. Chem. Theory Comput. 2016,
[S8] Mezei, P. D.; Ruzsinszky, A.; Csonka, G. I. J. Chem. Theory Comput. 2016,
  Tarcsay àkos  
J Med Chem. 2013, 56, pp. 1789-1795. (IF: 5.248)
J Med Chem. 2013, 56, 1789-1795. old. (IF: 5.248)
  MEZEI Pà¡l Dà¡niel  
[O3] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A. J. Chem. Theory Comput. 2015, 11,
[S3] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A. J. Chem. Theory Comput. 2015, 11,
  MEZEI Pà¡l Dà¡niel  
[O4] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Kállay, M. J. Chem. Theory Comput.
[S4] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Kállay, M. J. Chem. Theory Comput.
  MEZEI Pà¡l Dà¡niel  
Chem. Eng. 2016, 60, 2–7. (IF = 0.296, CT =2)
Chem. Eng. 2016, 60, 2-7. (IF = 0,296, ID =2)
  MEZEI Pà¡l Dà¡niel  
[O2] Mezei, P. D.; Csonka, G. I.; Kállay, M. J. Chem. Theory Comput. 2015, 11, 2879–2888.
[S2] Mezei, P. D.; Csonka, G. I.; Kállay, M. J. Chem. Theory Comput. 2015, 11, 2879-2888.
  Gyarmati Benjà¡min  
[GY8] Gyarmati B, Szilágyi A. Preface for papers presented at AMSALS 2012. Period. Polytech. Chem. Eng. 2013; 58(1):47-48. (IF 2012: 0.269, IC:0)
[GY8] Gyarmati B, Szilágyi A. Preface for papers presented at AMSALS 2012. Period. Polytech. Chem. Eng. 2013; 58(1):47-48. (IF 2012: 0,269, IC:0)
  Tarcsay àkos  
[11] Gleeson, M.P., Generation of a set of simple, interpretable ADMET rules of thumb. J Med Chem. 2008, 51 (4), pp. 817-834..
[11] Gleeson, M.P., Generation of a set of simple, interpretable ADMET rules of thumb.J Med Chem. 2008, 51 (4), 817-834. old.
  MEZEI Pà¡l Dà¡niel  
[O1] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Sun, J. J. Chem. Theory Comput. 2015,
[S1] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Sun, J. J. Chem. Theory Comput. 2015,
  Tarcsay àkos  
[T7] Tarcsay, A.; Nyíri, K.; Keserű, G.M., Impact of lipophilic efficiency on compound quality. J Med Chem. 2012, 55, pp. 1252-1260. (IF: 5.248)
[T7] Tarcsay, A.; Nyíri, K.; Keserű, G.M., Impact of lipophilic efficiency on compound quality. J Med Chem. 2012, 55, 1252-1260. old. (IF: 5.248)
  Tarcsay àkos  
[T4] Tarcsay, A.; Keserű, G.M., Homology modelling and binding site assessment of the human P-glycoprotein. Future Med Chem. 2011, 3,pp. 297-307. (IF:2.522)
[T4] Tarcsay, A., Keserű, G.M. Homology modeling and binding site assessment of the human P-glycoprotein. Future Med Chem. 2011, 3, 297-307. old. (IF:2.522)
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Tarcsay àkos  
[10] McGaughey, G.B.; Sheridan, R.P.; Bayly, C.I.; Culberson, J.C.; Kreatsoulas, C. ; Lindsley, S. ; Maiorov, V. ; Truchon, J.F.; Cornell, W.D., Comparison of topological, shape, and docking methods in virtual screening. J Chem Inf Model, 2007, 47, pp. 1504–1519.
[10] McGaughey, G.B.; Sheridan, R.P.; Bayly, C.I.; Culberson, J.C.; Kreatsoulas, C.; Lindsley, S.; Maiorov, V.; Truchon, J.F.; Cornell, W.D., Comparison of topological, shape, and docking methods in virtual screening. J Chem Inf Model, 2007, 47, 1504–1519. old.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am. Chem. Soc. 1995, 117, 825–826. d) S. Fau, G. Frenking, Mol. Phys. 1999, 96, 519–527. e) O. A. Filippov, A. M. Filin, V. N. Tsupreva, N. V. Belkova, A. Lledós, G. Ujaque, L. M. Epstein, E. S. Shubina, Inorg. Chem. 2006, 45, 3086–3096. f) C. Fan, L. G. Mercier, W. E. Piers, H. M. Tuononen, M. Parvez, J. Am. Chem. Soc. 2010, 132, 9604–9606. g) Z. Lu, Z. Cheng, Z. Chen, L. Weng, Z. H. Li, H. Wang, Angew. Chem. 2011, 123, 12435–12439; Angew. Chem. Int. Ed. 2011, 50, 12227–12231. h) G. I. Nikonov, S. F. Vyboishchikov, O. G. Shirobokov, J. Am. Chem. Soc. 2012, 134, 5488–5491. d) J.-L. M. Abboud, B. Németh, J.-C. Guillemin, P.Burk, A. Adamson, E. R. Nerut, Chem. Eur. J. 2012, 18, 3981–3991.
  Könczöl Là¡szlà³  
[10] a) T. J. Tague Jr., L. Andrews, J. Am. Chem. Soc. 1994, 116, 4970–4976. b) P. R. Schreiner, H. F. Schaefer III, P. v. R. Schleyer, J. Chem. Phys. 1994, 101, 7625–7632. c) J. D. Watts, R. J. Bartlett, J. Am.
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  Kiss Nà³ra Zsuzsa  
[7] D. R. Baghurst, D. M. P. Mingos, Chem. Soc. Rev., 1991, 20, 1-47.
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[K12] N. Zs. Kiss. É. V. Böttger, L. Drahos, G. Keglevich, Heteroatom Chem, 2013, 24, 283-288. page
[K13] Keglevich, G.; Kiss, N. Zs.; Körtvélyesi, T.; Mucsi Z., Phosphorus, Sulfur 2013, 188, 29-32. old.
  Kiss Nà³ra Zsuzsa  
[6] C. O. Kappe, Angew. Chem. Int. Ed., 2004, 43, 6250-628.
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[4] C. O. Kappe, B. Pieber, D. Dallinger, Angew. Chem. 2013, 52, 1088.
[4] C. O. Kappe, B. Pieber, D. Dallinger., Angew. Chem. 2013, 52, 1088.
  Mezei Pà¡l Dà¡niel  
[O4] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Kállay, M. J. Chem. Theory Comput. 2015 under revision. ct–2015–00420z
[S4] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Kállay, M. J. Chem. Theory Comput. 2015 felülvizsgálaton. ct–2015–00420z
  Kiss Nà³ra Zsuzsa  
[K8] G. Keglevich, A. Grün, E. Bálint, N. Zs. Kiss, E. Jablonkai, Curr. Org. Chem. 2013, 17, pp. 545-554.
[K9] Keglevich, G.; Kiss, N. Zs.; Körtvélyesi, T., Heteroatom Chem. 2013, nyomdában
  Kiss Nà³ra Zsuzsa  
[K9] G. Keglevich, N. Zs. Kiss, T. Körtvélyesi, Heteroatom Chem. 2013, in press
[K10] Keglevich, G.; Kiss, N. Zs.; Drahos, L.; Körtvélyesi, T., Tetrahedron Lett. 2013, 54, 466-469. old.
  Mà¡rkus Bence Gà¡bor  
[16] C. A. Kraus: Solutions of metals in non-metallic solvents; i. general properties of solutions of metals in liquid ammonia, J. Am. Chem. Soc. 29 (11), 1557–1571 (1907)
[16] C. A. Kraus: Solutions of metals in non-metallic solvents; i. general properties of solutions of metals in liquid ammonia, J. Am. Chem. Soc. 29 (11), 1557–1571 (1907).
  Kiss Nà³ra Zsuzsa  
[K5] G. Keglevich, N. Zs. Kiss, G.K. Menyhárd, A. Fehérvári, I. Csontos, Heteroatom Chem 2012, 23, pp. 171-178.
[K6] Kiss, N. Zs.; Kaszás A.; Drahos, L.; Mucsi, Z.; Keglevich, G., Tetrahedron Lett. 2012, 53, 207–209. old.
  Kiss Nà³ra Zsuzsa  
[K7] G. Keglevich, N. Zs. Kiss, Z. Mucsi, T. Körtvélyesi, Org. Biomol. Chem. 2012, 10, pp. 2011-2018.
[K8] Keglevich, G.; Grün, A.; Bálint, E.; Kiss, N. Zs.; Jablonkai, E., Curr. Org. Chem. 2013, 17, 545-554. old.
  Vigh Tamà¡s  
[2] S. Ferguson, G. Morris, H. Hao, M. Barrett, B. Glennon: Characterization of the anti-solvent batch, plug flow and MSMPR crystallization of benzoic acid, Chem. Eng. Sci. 104 (2013) pp. 44-54
[2] S. Ferguson, G. Morris, H. Hao, M. Barrett, B. Glennon, Characterization of the anti-solvent batch, plug flow and MSMPR crystallization of benzoic acid, Chem. Eng. Sci. 104 (2013) 44–54.
  Boros Zoltà¡n  
[B] E. Abaháziová, Z. Boros, P. Kovács, L. Poppe: Surface modification of silica gels for selective adsorption of bacterial lipases, Stud. Univ. Babes-Bolyai, Chem, 2012, accepted for publication
[A] M. Oláh, Z. Boros, P. Sátorhelyi, V. Bódai, E. Balázs, L. Poppe: Kinetic resolution of racemic 1-phenylethanamine catalyzed by lipase B from Candida antarctica – Effect of the acylating agent and the mode of enzyme immobilization, Stud. Univ. Babes-Bolyai, Chem, 2012, közlésre elfogadva
  Boros Zoltà¡n  
[G] Z. Boros, M. Szigeti, A. Tomin, P. Kovács, L. Ürge, F. Darvas, L. Poppe: Asymmetric biotransformations in continuous flow reactors, Stud. Univ. Babes-Bolyai, Chem, 2009, 54, 69-75.
[F] J. Brem, M. Naghi, M. Tosa, Z. Boros, L. Poppe, F. Irimie, C. Paizs: Lipase mediated sequential resolution of aromatic β-hydroxy esters using fatty acid derivatives, Tetrahedron: Asymmetry, 2011, 22, 1672-1679.
  Kiss Nà³ra Zsuzsa  
[K2] G. Keglevich, E. Bálint, N. Zs. Kiss, E. Jablonkai, L. Hegedűs, A. Grün, I. Greiner, Curr Org Chem 2011, 15, pp. 1802-1810.
[K3] Keglevich, G.; Kiss, N. Zs.; Balint E.; Jablonkai E.; Grün A.; Milen M.; Frigyes D.; Greiner I., Phosphorus, Sulfur, 2011, 186, 802-803. old.
  Mezei Pà¡l Dà¡niel  
[O3] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A. J. Chem. Theory Comput. 2015 just accepted, published online. ct–2015–00269g
[S3] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A. J. Chem. Theory Comput. 2015 most elfogadott, online közzétéve. ct–2015–00269g
  Mezei Pà¡l Dà¡niel  
[O1] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Sun, J. J. Chem. Theory Comput. 2015, 11, 360–371.
[S1] Mezei, P. D.; Csonka, G. I.; Ruzsinszky, A.; Sun, J. J. Chem. Theory Comput. 2015, 11, 360–371.
  Boros Zoltà¡n  
[E] P. Falus, Z. Boros, G. Hornyánszky, J. Nagy, L. Ürge, F. Darvas. L. Poppe: Synthesis and lipase catalysed kinetic resolution of racemic amines, Stud. Univ. Babes-Bolyai, Chem, 2010, 55, 289-296.
[D] G. Hellner, Z. Boros, A. Tomin, L. Poppe: Novel sol-gel lipases by designed bioimprinting for continuous-flow kinetic resolutions, Advanced Synthesis & Catalysis, 2011, 353, 2481-2491.
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