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Synlett 2014; 25(13): 1847-1850
DOI: 10.1055/s-0034-1378534
DOI: 10.1055/s-0034-1378534
letter
Hyperbranched Polyamines: Tunable Catalysts for the Henry Reaction
Weitere Informationen
Publikationsverlauf
Received: 12. April 2014
Accepted after revision: 27. Mai 2014
Publikationsdatum:
09. Juli 2014 (online)
Abstract
Hyperbranched polyethylenimine derivatives were successfully employed as catalyst in the Henry reaction. The nitroalcohol products were obtained in excellent yields within short reaction times. A one-pot synthesis of β-nitrostyrenes was developed by using ZnCl2 along with hyperbranched polyethylenimine derivatives.
Key words
Henry reaction - diastereoselectivity - polyamine - homogeneous catalysis - β-nitrostyreneSupporting Information
- for this article is available online at http://www.thieme-connect.com/products/ejournals/journal/ 10.1055/s-00000083.
- Supporting Information
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References
- 1 Fitch RW, Sturgeon GD, Patel SR, Spande TF, Garraffo HM, Daly JW, Blaauw RH. J. Nat. Prod. 2009; 72: 243
- 2 Kureshy RI, Das A, Khan NH, Abdi SH. R, Bajaj HC. ACS Catal. 2011; 1: 1529
- 3 Roy A, Reddy LA, Dwivedi N, Naram J, Swapna R, Malakondaiah GC, Ravikumar M, Bhalerao D, Pratap TB, Reddy PP, Bhattacharya A, Bandichhor R. Tetrahedron Lett. 2011; 52: 6968
- 4 Das A, Kureshy RI, Prathap KJ, Choudhary MK, Rao GV. S, Khan NH, Abdi SH. R, Bajaj HC. Appl. Catal., A. 2013; 459: 97
- 5 Ballini R, Palmieri A, Righi P. Tetrahedron 2007; 63: 12099 ; and references cited therein
- 6 Alizadeh A, Khodaei MM, Kordestani D, Fallah AH, Beygzadeh M. Microporous Mesoporous Mater. 2012; 159: 9
- 7 Ballini R, Noé M, Perosa A, Selva M. J. Org. Chem. 2008; 73: 8520
- 8 Khan FA, Dash J, Satapathy R, Upadhyay SK. Tetrahedron Lett. 2004; 45: 3055
- 9 Neelakandeswari N, Sangami G, Emayavaramban P, Karvembu R, Dharmaraj N, Kim HY. Tetrahedron Lett. 2012; 53: 2980
- 10 Devi R, Borah R, Deka RC. Appl. Catal., A 2012; 433–434: 122
- 11 Ren Y, Cai C. Catal. Lett. 2007; 118: 134
- 12 Kühbeck D, Dhar BB, Schön E.-M, Cativiela C, Gotor-Fernández V, Díaz DD. Beilstein J. Org. Chem. 2013; 9: 1111
- 13 Majhi A, Kadam ST, Kim SS. Bull. Korean Chem. Soc. 2009; 30: 1767
- 14 Liu J, Ren C, Yang Z, Shi W. J. Polym. Sci., Part A: Polym. Chem. 2007; 45: 699
- 15 Magar RL, Thorat PB, Jadhav VB, Tekale SU, Dake SA, Patil BR, Pawar RP. J. Mol. Catal. A: Chem. 2013; 374–375: 118
- 16 Kano T, Konishi S, Shirakawa S, Maruoka K. Tetrahedron: Asymmetry 2004; 15: 1243
- 17 Shiraishi Y, Ichimura C, Hirai T. Tetrahedron Lett. 2007; 48: 7769
- 18a Levine M, Kenesky CS, Zheng S, Quinn J, Breslow R. Tetrahedron Lett. 2008; 49: 5746
- 18b Jurčík V, Wilhelm R. Tetrahedron 2004; 60: 3205
- 19 Rodríguez JM, Pujol MD. Tetrahedron Lett. 2011; 52: 2629
- 20 Rokhum L, Bez G. Tetrahedron Lett. 2013; 54: 5500
- 21 Bandgar BP, Uppalla LS, Sadavarte VS. Monatsh. Chem. 2000; 131: 949
- 22 Maity S, Manna S, Rana S, Naveen T, Mallick A, Maiti D. J. Am. Chem. Soc. 2013; 135: 3355
- 23 Solomonovici A, Blumberg S. Tedrahedron 1966; 22: 2505