Three consecutive steps over the chirally modified Pt surface: Asymmetric catalytic cascade reaction of 2-nitrophenylpyruvates

Catalysis Science and Technology

Volumn 5, Issue 2, 2015, Pages 697-704

  Szollosi, György ^a   Kovács, Lenke ^b   Makra, Zsolt ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

^b UNIVERSITY OF SZEGED   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS;

CASCADE REACTIONS; EFFECT OF H; ENANTIOSELECTIVE HYDROGENATION; KETO GROUPS; NITRO-GROUP REDUCTIONS; PT CATALYSTS; REACTION CONDITIONS; SUBSTRATE CONCENTRATIONS;

PLATINUM;

EID: 84927802607     PISSN: 20444753     EISSN: 20444761     Source Type: Journal    
DOI: 10.1039/c4cy00883a     Document Type: Article

References (44)

1. Heterocycles in Natural Product Synthesis, ed. K. C. Majumdar and S. K. Chattopadhyay, Wiley-VCH, Weinheim, 2011.
2. Chiral Drugs: Chemistry and Biological Action, ed. G.-Q. Lin, Q.-D. You and J.-F. Cheng, John Wiley & Sons, Hoboken, New Jersey, 2011.
3. V. Sridharan, P. A. Suryavanshi and J. C. Menéndez, Chem. Rev., 2011, 111, 7157-7259.
4. Y.-G. Zhou, Acc. Chem. Res., 2007, 40, 1357-1366.
5. H. Pellissier, Adv. Synth. Catal., 2012, 354, 237-294.
6. H. Clavier and H. Pellissier, Adv. Synth. Catal., 2012, 354, 3347-3403.
7. L.-Q. Lu, J.-R. Chen and W.-J. Xiao, Acc. Chem. Res., 2012, 45, 1278-1293.
8. Handbook of Asymmetric Heterogeneous Catalysis, ed. K. Ding and Y. Uozumi, Wiley-VCH, Weinheim, 2008.
9. T. Mallat, E. Orglmeister and A. Baiker, Chem. Rev., 2007, 107, 4863-4890.
10. D. Yu. Murzin, P. Mäki-Arvela, E. Toukoniitty and T. Salmi, Catal. Rev.: Sci. Eng., 2005, 47, 175-256.
11. M. Bartók, Curr. Org. Chem., 2006, 10, 1533-1567.
12. H.-U. Blaser and M. Studer, Acc. Chem. Res., 2007, 40, 1348-1356.
13. Gy. Szocombining double acute accentllocombining double acute accentsi, B. Hermán, K. Felföldi, F. Fülöp and M. Bartók, Adv. Synth. Catal., 2008, 350, 2804-2814.
14. J. Muzart, F. Hénin and S. J. Aboulhoda, Tetrahedron: Asymmetry, 1997, 8, 381-389.
15. L. Deiana, S. Afewerki, C. Palo-Nieto, O. Verho, E. V. Johnston and A. Córdova, Sci. Rep., 2012, 2, 851.
16. K. Felföldi, K. Szocombining double acute accentri and M. Bartók, Appl. Catal., A, 2003, 251, 457-460.
17. Gy. Szocombining double acute accentllocombining double acute accentsi and M. Bartók, ARKIVOC, 2012, (v), 16-27.
18. Gy. Szocombining double acute accentllocombining double acute accentsi, Zs. Makra, L. Kovács, F. Fülöp and M. Bartók, Adv. Synth. Catal., 2013, 355, 1623-1629.
19. H. Suzuki, H. Gyoutoku, H. Yokoo, M. Shinba, Y. Sato, H. Yamada and Y. Murakami, Synlett, 2000, 1196-1198.
20. M. Garland and H.-U. Blaser, J. Am. Chem. Soc., 1990, 112, 7048-7050.
21. Gy. Szocombining double acute accentllocombining double acute accentsi, Sz. Cserényi, F. Fülöp and M. Bartók, J. Catal., 2008, 260, 245-253.
22. M. von Arx, T. Mallat and A. Baiker, J. Catal., 2000, 193, 161-164.
23. C. Exner, A. Pfaltz, S. Studer and H.-U. Blaser, Adv. Synth. Catal., 2003, 345, 1253-1260.
24. B. Schimmoeller, F. Hoxha, T. Mallat, F. Krumeich, S. E. Pratsinis and A. Baiker, Appl. Catal., A, 2010, 374, 48-57.
25. T. Cseri, S. Békássy, F. Figueras, E. Cseke, L.-C. de Menorval and R. Dutartre, Appl. Catal., A, 1995, 132, 141-155.
26. M. A. Harmer and Q. Sun, Appl. Catal., A, 2001, 221, 45-62.
27. J. A. Cecilia, I. Jiménez-Morales, A. Infantes-Molina, E. Rodríguez-Castellón and A. Jiménez-López, J. Mol. Catal. A: Chem., 2013, 368-369, 78-87.
28. Gy. Szocombining double acute accentllocombining double acute accentsi, Á. Mastalir, Á. Molnár and M. Bartók, React. Kinet. Catal. Lett., 1996, 57, 29-36.
29. Gy. Szocombining double acute accentllocombining double acute accentsi, B. Török, L. Baranyi and M. Bartók, J. Catal., 1998, 179, 619-623.
30. S. Nishimura, Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis, John Wiley & Sons, Hoboken, New Jersey, 2011, ch. 9, pp. 315-389.
31. H. U. Blaser, U. Siegrist, H. Steiner and M. Studer, Fine Chemicals through Heterogeneous Catalysis, ed. R. A. Sheldon and H. van Bekkum, Wiley-VCH, Weinheim, 2001, pp. 389-406.
32. H. U. Blaser, H. P. Jalett and J. Wiehl, J. Mol. Catal., 1991, 68, 215-222.
33. K. Balázsik, K. Szocombining double acute accentri, Gy. Szocombining double acute accentllocombining double acute accentsi and M. Bartók, Chem. Commun., 2011, 47, 1551-1552.
34. K. Balázsik, K. Szocombining double acute accentri, Gy. Szocombining double acute accentllocombining double acute accentsi and M. Bartók, Catal. Commun., 2011, 12, 1410-1414.
35. U. K. Singh, R. N. Landau, Y. Sun, C. LeBlond, D. G. Blackmond, S. K. Tanielyan and R. L. Augustine, J. Catal., 1995, 154, 91-97.
36. Q. Chen, S. Haq, B. G. Frederick and N. V. Richardson, Surf. Sci., 1996, 368, 310-317.
37. A. Vargas, S. Reimann, S. Diezi, T. Mallat and A. Baiker, J. Mol. Catal. A: Chem., 2008, 282, 1-8.
38. M. Casagrande, S. Franceschini, M. Lenarda, O. Piccolo and A. Vaccari, J. Mol. Catal. A: Chem., 2006, 246, 263-267.
39. E. R. Blout and D. C. Silverman, J. Am. Chem. Soc., 1944, 66, 1442-1443.
40. S. Santiago-Pedro, V. Tamayo-Galván and T. Viveros-García, Catal. Today, 2013, 213, 101-108.
41. Gy. Szocombining double acute accentllocombining double acute accentsi, P. Forgó and M. Bartók, Chirality, 2003, 15, S82-S89.
42. D. Ferri and T. Bürgi, J. Am. Chem. Soc., 2001, 123, 12074-12084.
43. D. Ferri, T. Bürgi and A. Baiker, J. Catal., 2002, 210, 160-170.
44. M. Bartók, M. Sutyinszki, K. Balázsik and G. Szocombining double acute accentllocombining double acute accentsi, Catal. Lett., 2005, 100, 161-167.