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Volumn 3, Issue 2, 2013, Pages 386-389

Solvent-controlled, regio-switchable formation of 3-/5-arylaminopyrazole isomer in cyclocondensation of β-aminoenones with hydrazides: Intermolecular hydrogen bonding plays a role

(7) Xiang, Dexuan a Bi, Xihe b,c Liao, Peiqiu b Fang, Guichun b Wang, Zikun b Xin, Xiaoqing a Dong, Dewen a,b

a CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY (China)

b NORTHEAST NORMAL UNIVERSITY (China)

c NANKAI UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOCONDENSATION; HYDRAZINE HYDRATE; INTERMOLECULAR HYDROGEN BONDING; PYRAZOLES; REACTION SOLVENTS; REGIOISOMERS;

HYDRATES; HYDROGEN BONDS;

SOLVENTS;

EID: 84870923961 PISSN: None EISSN: 20462069 Source Type: Journal
DOI: 10.1039/c2ra22647b Document Type: Article

Times cited : (12)

References (40)

1
- 79958200235
- See aslo
- A. Schmidt A. Dreger Curr. Org. Chem. 2011 15 1423 1463
- (2011) Curr. Org. Chem. , vol.15 , pp. 1423-1463
- Schmidt, A.¹ Dreger, A.²

2
- 20944448138
- P. Pevarello M. G. Brasca P. Orsini G. Traquandi A. Longo M. Nesi F. Orzi C. Piutti P. Sansonna M. Varasi A. Cameron A. Vulpetti F. Roletto R. Alzani M. Ciomei C. Albanese W. Pastori A. Marsiglio E. Pesenti F. Fiorentini J. R. Bischoff C. Mercurio J. Med. Chem. 2005 48 2944 2956
- (2005) J. Med. Chem. , vol.48 , pp. 2944-2956
- Pevarello, P.¹ Brasca, M.G.² Orsini, P.³ Traquandi, G.⁴ Longo, A.⁵ Nesi, M.⁶ Orzi, F.⁷ Piutti, C.⁸ Sansonna, P.⁹ Varasi, M.¹⁰ Cameron, A.¹¹ Vulpetti, A.¹² Roletto, F.¹³ Alzani, R.¹⁴ Ciomei, M.¹⁵ Albanese, C.¹⁶ Pastori, W.¹⁷ Marsiglio, A.¹⁸ Pesenti, E.¹⁹ Fiorentini, F.²⁰ Bischoff, J.R.²¹ Mercurio, C.²² more..

3
- 44149100766
- A. Hall A. Billinton S. H. Brown N. M. Clayton A. Chowdhury G. M. P. Giblin P. Goldsmith T. G. Hayhow D. N. Hurst I. R. Kilford A. Naylor B. Passingham L. Winyard Bioorg. Med. Chem. Lett. 2008 18 3392 3399
- (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 3392-3399
- Hall, A.¹ Billinton, A.² Brown, S.H.³ Clayton, N.M.⁴ Chowdhury, A.⁵ Giblin, G.M.P.⁶ Goldsmith, P.⁷ Hayhow, T.G.⁸ Hurst, D.N.⁹ Kilford, I.R.¹⁰ Naylor, A.¹¹ Passingham, B.¹² Winyard, L.¹³

4
- 67649984195
- For general reviews on the synthesis of pyrazoles, please see
- P. J. Skinner P. J. Webb C. R. Sage H. T. Dang C. C. Pride R. Chen S. Y. Tamura J. G. Richman D. T. Connolly G. Semple Bioorg. Med. Chem. Lett. 2009 19 4207 4209
- (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 4207-4209
- Skinner, P.J.¹ Webb, P.J.² Sage, C.R.³ Dang, H.T.⁴ Pride, C.C.⁵ Chen, R.⁶ Tamura, S.Y.⁷ Richman, J.G.⁸ Connolly, D.T.⁹ Semple, G.¹⁰

5
- 80755168455
- S. Fustero M. Sánchez-Roselló P. Barrio A. Simón-Fuentes Chem. Rev. 2011 111 6984 7034
- (2011) Chem. Rev. , vol.111 , pp. 6984-7034
- Fustero, S.¹ Sánchez-Roselló, M.² Barrio, P.³ Simón-Fuentes, A.⁴

6
- 84865089156
- For a review focused on regioselective synthesis of pyrazoles, please see
- Y. L. Janin Chem. Rev. 2012 112 3924 3958
- (2012) Chem. Rev. , vol.112 , pp. 3924-3958
- Janin, Y.L.¹

7
- 79951704638
- J.-Y. Yoon S.-G. Lee H. Shin Curr. Org. Chem. 2011 15 657 674
- (2011) Curr. Org. Chem. , vol.15 , pp. 657-674
- Yoon, J.-Y.¹ Lee, S.-G.² Shin, H.³

8
- 84980107215
- For recent examples, see
- L. Knorr Ber 1883 16 2597 2599
- (1883) Ber , vol.16 , pp. 2597-2599
- Knorr, L.¹

9
- 68049092045
- Y. Zhao A. Bacher B. Illarionov M. Fischer G. Georg Q.-Z. Ye P. E. Fanwick S. G. Franzblau B. Wan M. Cushman J. Org. Chem. 2009 74 5297 5303
- (2009) J. Org. Chem. , vol.74 , pp. 5297-5303
- Zhao, Y.¹ Bacher, A.² Illarionov, B.³ Fischer, M.⁴ Georg, G.⁵ Ye, Q.-Z.⁶ Fanwick, P.E.⁷ Franzblau, S.G.⁸ Wan, B.⁹ Cushman, M.¹⁰

10
- 51549101998
- J. P. Waldo S. Mehta R. C. Larock J. Org. Chem. 2008 73 6666 6670
- (2008) J. Org. Chem. , vol.73 , pp. 6666-6670
- Waldo, J.P.¹ Mehta, S.² Larock, R.C.³

11
- 67651172803
- G. A. Idrees O. M. Aly G. E.-D. A. A. Abuo-Rahma M. F. Radwan Eur. J. Med. Chem. 2009 44 3973 3980
- (2009) Eur. J. Med. Chem. , vol.44 , pp. 3973-3980
- Idrees, G.A.¹ Aly, O.M.² Abuo-Rahma, G.E.-D.A.A.³ Radwan, M.F.⁴

12
- 77950327393
- For selected examples, please see
- M. A. P. Martins P. H. Beck D. N. Moreira L. Buriol C. P. Frizzo N. Zanatta H. G. Bonacorso J. Heterocycl. Chem. 2010 47 301 308
- (2010) J. Heterocycl. Chem. , vol.47 , pp. 301-308
- Martins, M.A.P.¹ Beck, P.H.² Moreira, D.N.³ Buriol, L.⁴ Frizzo, C.P.⁵ Zanatta, N.⁶ Bonacorso, H.G.⁷

13
- 74049124899
- L. Meng B. A. Lorsbach T. C. Sparks J. C. Fettinger M. J. Kurth J. Comb. Chem. 2010 12 129 136
- (2010) J. Comb. Chem. , vol.12 , pp. 129-136
- Meng, L.¹ Lorsbach, B.A.² Sparks, T.C.³ Fettinger, J.C.⁴ Kurth, M.J.⁵

14
- 84864619097
- S. Guo J. Wang D. Guo X. Zhang X. Fan Tetrahedron 2012 68 7768 7774
- (2012) Tetrahedron , vol.68 , pp. 7768-7774
- Guo, S.¹ Wang, J.² Guo, D.³ Zhang, X.⁴ Fan, X.⁵

15
- 33746105769
- S. T. Heller S. R. Natarajan Org. Lett. 2006 8 2675 2678
- (2006) Org. Lett. , vol.8 , pp. 2675-2678
- Heller, S.T.¹ Natarajan, S.R.²

16
- 10044290716
- R. Kowalczyk J. Skarzewski Tetrahedron 2005 61 623 628
- (2005) Tetrahedron , vol.61 , pp. 623-628
- Kowalczyk, R.¹ Skarzewski, J.²

17
- 84856722589
- G. C. Nandi M. S. Singh H. Ila H. Junjappa Eur. J. Org. Chem. 2012 967 974
- (2012) Eur. J. Org. Chem. , pp. 967-974
- Nandi, G.C.¹ Singh, M.S.² Ila, H.³ Junjappa, H.⁴

18
- 80054967867
- W. Jin H. Yu Z. Yu Tetrahedron Lett. 2011 52 5884 5887
- (2011) Tetrahedron Lett. , vol.52 , pp. 5884-5887
- Jin, W.¹ Yu, H.² Yu, Z.³

19
- 40949162436
- L. J. Kennedy Synlett 2008 600 604
- (2008) Synlett , pp. 600-604
- Kennedy, L.J.¹

20
- 27744591612
- S. Peruncheralathan A. K. Yadav H. Ila H. Junjappa J. Org. Chem. 2005 70 9644 9647
- (2005) J. Org. Chem. , vol.70 , pp. 9644-9647
- Peruncheralathan, S.¹ Yadav, A.K.² Ila, H.³ Junjappa, H.⁴

21
- 0004018410
- Eds, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim For examples of solvent-controlled selective organic reactions, see
- Solvents and Solvent Effects in Organic Chemistry, Fourth Edition, C. Reichardt, and, T. Welton, Eds, 2011, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
- (2011) Solvents and Solvent Effects in Organic Chemistry, Fourth Edition
- Reichardt, C.¹ Welton, T.²

22
- 67650323881
- Y. Ye C. Zheng R. Fan Org. Lett. 2009 11 3156 3159
- (2009) Org. Lett. , vol.11 , pp. 3156-3159
- Ye, Y.¹ Zheng, C.² Fan, R.³

23
- 79251510252
- A. W. Garner C. F. Harris D. A. K. Vezzu R. D. Pike S. Huo Chem. Commun. 2011 47 1902 1904
- (2011) Chem. Commun. , vol.47 , pp. 1902-1904
- Garner, A.W.¹ Harris, C.F.² Vezzu, D.A.K.³ Pike, R.D.⁴ Huo, S.⁵

24
- 60949092352
- For an example of regulating the ratio of isomers by the solvent, see
- L. Hintermann R. Masuo K. Suzuki Org. Lett. 2008 10 4859 4862
- (2008) Org. Lett. , vol.10 , pp. 4859-4862
- Hintermann, L.¹ Masuo, R.² Suzuki, K.³

25
- 33845603533
- F. Gosselin P. D. O'Shea R. A. Webster R. A. Reamer R. D. Tillyer E. J. J. Grabowski Synlett 2006 3267 3270
- (2006) Synlett , pp. 3267-3270
- Gosselin, F.¹ O'Shea, P.D.² Webster, R.A.³ Reamer, R.A.⁴ Tillyer, R.D.⁵ Grabowski, E.J.J.⁶

26
- 83455218228
- Y. Hu X. Fu B.-D. Barry X. Bi D. Dong Chem. Commun. 2012 48 690 692
- (2012) Chem. Commun. , vol.48 , pp. 690-692
- Hu, Y.¹ Fu, X.² Barry, B.-D.³ Bi, X.⁴ Dong, D.⁵

27
- 84862535442
- Z. Wang X. Bi P. Liao R. Zhang Y. Liang D. Dong Chem. Commun. 2012 48 7076 7078
- (2012) Chem. Commun. , vol.48 , pp. 7076-7078
- Wang, Z.¹ Bi, X.² Liao, P.³ Zhang, R.⁴ Liang, Y.⁵ Dong, D.⁶

28
- 84862917313
- D. Xiang X. Xin X. Liu R. Zhang J. Yang D. Dong Org. Lett. 2012 14 644 647
- (2012) Org. Lett. , vol.14 , pp. 644-647
- Xiang, D.¹ Xin, X.² Liu, X.³ Zhang, R.⁴ Yang, J.⁵ Dong, D.⁶

29
- 84855504645
- P. Huang N. Zhang R. Zhang D. Dong Org. Lett. 2012 14 370 373
- (2012) Org. Lett. , vol.14 , pp. 370-373
- Huang, P.¹ Zhang, N.² Zhang, R.³ Dong, D.⁴

30
- 78651406983
- Y. Wang X. Bi D. Li P. Liao Y. Wang J. Yang Q. Zhang Q. Liu Chem. Commun. 2011 47 809 811
- (2011) Chem. Commun. , vol.47 , pp. 809-811
- Wang, Y.¹ Bi, X.² Li, D.³ Liao, P.⁴ Wang, Y.⁵ Yang, J.⁶ Zhang, Q.⁷ Liu, Q.⁸

31
- 77956306336
- Y. Wang W.-Q. Li G. Che X. Bi P. Liao Q. Zhang Q. Liu Chem. Commun. 2010 46 6843 6845
- (2010) Chem. Commun. , vol.46 , pp. 6843-6845
- Wang, Y.¹ Li, W.-Q.² Che, G.³ Bi, X.⁴ Liao, P.⁵ Zhang, Q.⁶ Liu, Q.⁷

32
- 62749094399
- K. Wang X. Fu J. Liu Y. Liang D. Dong Org. Lett. 2009 11 1015 1018
- (2009) Org. Lett. , vol.11 , pp. 1015-1018
- Wang, K.¹ Fu, X.² Liu, J.³ Liang, Y.⁴ Dong, D.⁵

33
- 48849112035
- K. Wang D. Xiang J. Liu W. Pan D. Dong Org. Lett. 2008 10 1691 1694
- (2008) Org. Lett. , vol.10 , pp. 1691-1694
- Wang, K.¹ Xiang, D.² Liu, J.³ Pan, W.⁴ Dong, D.⁵

34
- 35948940824
- X. Bi J. Zhang Q. Liu J. Tan B. Li Adv. Synth. Catal. 2007 349 2301 2306
- (2007) Adv. Synth. Catal. , vol.349 , pp. 2301-2306
- Bi, X.¹ Zhang, J.² Liu, Q.³ Tan, J.⁴ Li, B.⁵

35
- 16844377947
- For a similar pyrazole derivative, see
- X. Bi D. Dong Q. Liu W. Pan L. Zhao B. Li J. Am. Chem. Soc. 2005 127 4578 4579
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 4578-4579
- Bi, X.¹ Dong, D.² Liu, Q.³ Pan, W.⁴ Zhao, L.⁵ Li, B.⁶

36
- 0035188179
- L. Song Q. Chu S. Zhu J. Fluor. Chem. 2001 107 107 112
- (2001) J. Fluor. Chem. , vol.107 , pp. 107-112
- Song, L.¹ Chu, Q.² Zhu, S.³

37
- 81255147926
- H. Khalilullah S. Khan M. J. Ahsan B. Ahmed Bioorg. Med. Chem. Lett. 2011 21 7251 7254
- (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 7251-7254
- Khalilullah, H.¹ Khan, S.² Ahsan, M.J.³ Ahmed, B.⁴

38
- 80955145694
- D. Zhang G. Wang G. Zhao W. Xu L. Huo Eur. J. Med. Chem. 2011 46 5868 5877
- (2011) Eur. J. Med. Chem. , vol.46 , pp. 5868-5877
- Zhang, D.¹ Wang, G.² Zhao, G.³ Xu, W.⁴ Huo, L.⁵

39
- 80655144324
- M. Pitucha U. Kosikowska L. Urszula A. Malm Med. Chem. 2011 7 697 703
- (2011) Med. Chem. , vol.7 , pp. 697-703
- Pitucha, M.¹ Kosikowska, U.² Urszula, L.³ Malm, A.⁴

40
- 84961980498
- references cited therein
- A. Lévai A. M. S. Silva J. A. S. Cavaleiro I. Alkorta J. Elguero J. Jekö Eur. J. Org. Chem. 2006 2825 2832
- (2006) Eur. J. Org. Chem. , pp. 2825-2832
- Lévai, A.¹ Silva, A.M.S.² Cavaleiro, J.A.S.³ Alkorta, I.⁴ Elguero, J.⁵ Jekö, J.⁶

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