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Volumn 15, Issue 2, 2013, Pages 490-495

Solvent-free Huisgen cyclization using heterogeneous copper catalysts supported on chelate resins

(8) Monguchi, Yasunari a Nozaki, Kei a Maejima, Toshihide a Shimoda, Yutaka a Sawama, Yoshinari a Kitamura, Yoshiaki b Kitade, Yukio b Sajiki, Hironao a

a GIFU PHARMACEUTICAL UNIVERSITY (Japan)

b GIFU UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84873324490 PISSN: 14639262 EISSN: 14639270 Source Type: Journal
DOI: 10.1039/c2gc36584g Document Type: Article

Times cited : (34)

References (58)

1
- 84981452695
- R. Huisgen G. Szeimies L. Moebius Chem. Ber. 1967 100 2494 2507
- (1967) Chem. Ber. , vol.100 , pp. 2494-2507
- Huisgen, R.¹ Szeimies, G.² Moebius, L.³

2
- 0002490493
- in, ed. A. Padowa, Wiley, New York
- R. Huisgen, in 1,3-Dipolar Cycloaddition Chemistry, ed., A. Padowa, Wiley, New York, 1984, pp. 1-176
- (1984) 1,3-Dipolar Cycloaddition Chemistry , pp. 1-176
- Huisgen, R.¹

3
- 0037012920
- C. W. Tornøe C. Christensen M. Meldal J. Org. Chem. 2002 67 3057 3064
- (2002) J. Org. Chem. , vol.67 , pp. 3057-3064
- Tornøe, C.W.¹ Christensen, C.² Meldal, M.³

4
- 0013064237
- Angew. Chem., Int. Ed. 2002 41 2596 2599 For reviews
- V. V. Rostovtsev L. G. Green V. V. Fokin K. B. Sharpless Angew. Chem. 2002 114 2708 2711 Angew. Chem., Int. Ed. 2002 41 2596 2599
- (2002) Angew. Chem. , vol.114 , pp. 2708-2711
- Rostovtsev, V.V.¹ Green, L.G.² Fokin, V.V.³ Sharpless, K.B.⁴

5
- 84867726453
- V. D. Bock H. Hiemstra J. H. van Maarseveen Eur. J. Org. Chem. 2006 51 68
- (2006) Eur. J. Org. Chem. , pp. 51-68
- Bock, V.D.¹ Hiemstra, H.² Van Maarseveen, J.H.³

6
- 51049094897
- M. Meldal C. W. Tornøe Chem. Rev. 2008 108 2952 3015
- (2008) Chem. Rev. , vol.108 , pp. 2952-3015
- Meldal, M.¹ Tornøe, C.W.²

7
- 0000749443
- Angew. Chem., Int. Ed. 2001 40 2004 2021
- H. C. Kolb M. G. Finn K. B. Sharpless Angew. Chem. 2001 113 2056 2075 Angew. Chem., Int. Ed. 2001 40 2004 2021
- (2001) Angew. Chem. , vol.113 , pp. 2056-2075
- Kolb, H.C.¹ Finn, M.G.² Sharpless, K.B.³

8
- 0348109450
- H. C. Kolb K. B. Sharpless Drug Discovery Today 2003 8 1128 1137
- (2003) Drug Discovery Today , vol.8 , pp. 1128-1137
- Kolb, H.C.¹ Sharpless, K.B.²

9
- 33846893890
- L. Yin J. Liebscher Chem. Rev. 2007 107 133 173
- (2007) Chem. Rev. , vol.107 , pp. 133-173
- Yin, L.¹ Liebscher, J.²

10
- 79951685909
- M. J. Climent A. Corma S. Iborra Chem. Rev. 2011 111 1072 1133
- (2011) Chem. Rev. , vol.111 , pp. 1072-1133
- Climent, M.J.¹ Corma, A.² Iborra, S.³

11
- 84890664985
- 2nd edn ed., Wiley-VCH, Weinheim
- Solvent-free Organic Synthesis, ed., K. Tanaka, 2nd edn, Wiley-VCH, Weinheim, 2008
- (2008) Solvent-free Organic Synthesis
- Tanaka, K.¹

12
- 80053584926
- ed., Springer, Berlin
- Topics Current Chemistry 254, Organic Solid State Reactions, ed., F. Toda, Springer, Berlin, 2005
- (2005) Topics Current Chemistry 254, Organic Solid State Reactions
- Toda, F.¹

13
- 0000361316
- D. C. Dittmer Chem. Ind. 1997 19 779 784
- (1997) Chem. Ind. , vol.19 , pp. 779-784
- Dittmer, D.C.¹

14
- 0033444261
- R. S. Varma Green Chem. 1999 1 43 55
- (1999) Green Chem. , vol.1 , pp. 43-55
- Varma, R.S.¹

15
- 0000884192
- K. Tanaka F. Toda Chem. Rev. 2000 100 1025 1074
- (2000) Chem. Rev. , vol.100 , pp. 1025-1074
- Tanaka, K.¹ Toda, F.²

16
- 0035742525
- R. S. Varma Pure Appl. Chem. 2001 73 193 198
- (2001) Pure Appl. Chem. , vol.73 , pp. 193-198
- Varma, R.S.¹

17
- 34447102708
- P. J. Walsh H. Li C. A. de Parrodi Chem. Rev. 2007 107 2503 2545
- (2007) Chem. Rev. , vol.107 , pp. 2503-2545
- Walsh, P.J.¹ Li, H.² De Parrodi, C.A.³

18
- 70349386397
- M. A. P. Martins C. P. Frizzo D. N. Moreira L. Buriol P. Machado Chem. Rev. 2009 109 4140 4182
- (2009) Chem. Rev. , vol.109 , pp. 4140-4182
- Martins, M.A.P.¹ Frizzo, C.P.² Moreira, D.N.³ Buriol, L.⁴ MacHado, P.⁵

19
- 80053593399
- For non-supported heterogeneous copper catalysts
- Y. Monguchi Y. Fujita S. Hashimoto M. Ina T. Takahashi R. Ito K. Nozaki T. Maegawa H. Sajiki Tetrahedron 2011 67 8628 8634
- (2011) Tetrahedron , vol.67 , pp. 8628-8634
- Monguchi, Y.¹ Fujita, Y.² Hashimoto, S.³ Ina, M.⁴ Takahashi, T.⁵ Ito, R.⁶ Nozaki, K.⁷ Maegawa, T.⁸ Sajiki, H.⁹

20
- 77956377240
- S. K. Yousuf D. Mukherjee B. Singh S. Maity S. C. Taneja Green Chem. 2010 12 1568 1572
- (2010) Green Chem. , vol.12 , pp. 1568-1572
- Yousuf, S.K.¹ Mukherjee, D.² Singh, B.³ Maity, S.⁴ Taneja, S.C.⁵

21
- 77949723565
- B. R. Buckley S. E. Dann D. P. Harris H. Heaney E. C. Stubbs Chem. Commun. 2010 46 2274 2276
- (2010) Chem. Commun. , vol.46 , pp. 2274-2276
- Buckley, B.R.¹ Dann, S.E.² Harris, D.P.³ Heaney, H.⁴ Stubbs, E.C.⁵

22
- 78049329140
- I. Luz F. X. L. i Xamena A. Corma J. Catal. 2010 276 134 140
- (2010) J. Catal. , vol.276 , pp. 134-140
- Luz, I.¹ Xamena, F.X.L.I.² Corma, A.³

23
- 34948874398
- Angew. Chem., Int. Ed. 2006 45 8235 8238
- B. H. Lipshuz B. R. Taft Angew. Chem. 2006 118 8415 8418 Angew. Chem., Int. Ed. 2006 45 8235 8238
- (2006) Angew. Chem. , vol.118 , pp. 8415-8418
- Lipshuz, B.H.¹ Taft, B.R.²

24
- 34948861725
- P. Cintas K. Martina B. Robaldo D. Garella L. Boffa G. Cravotto Collect. Czech. Chem. Commun. 2007 72 1014 1024
- (2007) Collect. Czech. Chem. Commun. , vol.72 , pp. 1014-1024
- Cintas, P.¹ Martina, K.² Robaldo, B.³ Garella, D.⁴ Boffa, L.⁵ Cravotto, G.⁶

25
- 58549087740
- H. Sharghi R. Khalifeh M. M. Doroodmand Adv. Synth. Catal. 2009 351 207 218
- (2009) Adv. Synth. Catal. , vol.351 , pp. 207-218
- Sharghi, H.¹ Khalifeh, R.² Doroodmand, M.M.³

26
- 78049291325
- H. Kang H. J. Lee J. C. Park H. Song K. H. Park Top. Catal. 2010 53 523 528
- (2010) Top. Catal. , vol.53 , pp. 523-528
- Kang, H.¹ Lee, H.J.² Park, J.C.³ Song, H.⁴ Park, K.H.⁵

27
- 80052217450
- F. Alonso Y. Noglie G. Radivoy M. Yus Org. Biomol. Chem. 2011 9 6385 6395
- (2011) Org. Biomol. Chem. , vol.9 , pp. 6385-6395
- Alonso, F.¹ Noglie, Y.² Radivoy, G.³ Yus, M.⁴

28
- 33947099937
- S. Chassaing M. Kumarraja A. S. S. Sido P. Pale J. Sommer Org. Lett. 2007 9 883 886
- (2007) Org. Lett. , vol.9 , pp. 883-886
- Chassaing, S.¹ Kumarraja, M.² Sido, A.S.S.³ Pale, P.⁴ Sommer, J.⁵

29
- 48049096809
- A. Alix S. Chassaing P. Pale J. Sommer Tetrahedron 2008 64 8922 8929
- (2008) Tetrahedron , vol.64 , pp. 8922-8929
- Alix, A.¹ Chassaing, S.² Pale, P.³ Sommer, J.⁴

30
- 53849092694
- S. Chassaing A. S. S. Sido A. Alix M. Kumarraja P. Pale J. Sommer Chem.-Eur. J. 2008 14 6713 6721
- (2008) Chem.-Eur. J. , vol.14 , pp. 6713-6721
- Chassaing, S.¹ Sido, A.S.S.² Alix, A.³ Kumarraja, M.⁴ Pale, P.⁵ Sommer, J.⁶

31
- 77955362853
- S. Chassaing A. Alix T. Boningari K. S. S. Sido M. Keller P. Kuhn B. Louis J. Sommer P. Pale Synthesis 2010 1557 1567
- (2010) Synthesis , pp. 1557-1567
- Chassaing, S.¹ Alix, A.² Boningari, T.³ Sido, K.S.S.⁴ Keller, M.⁵ Kuhn, P.⁶ Louis, B.⁷ Sommer, J.⁸ Pale, P.⁹

32
- 77954348910
- V. Bénéteau A. Olmos T. Boningari J. Sommer P. Pale Tetrahedron Lett. 2010 51 3673 3677
- (2010) Tetrahedron Lett. , vol.51 , pp. 3673-3677
- Bénéteau, V.¹ Olmos, A.² Boningari, T.³ Sommer, J.⁴ Pale, P.⁵

33
- 39349087593
- T. Miao L. Wang Synthesis 2008 363 368
- (2008) Synthesis , pp. 363-368
- Miao, T.¹ Wang, L.²

34
- 77952878761
- T. Shamin S. Paul Catal. Lett. 2010 136 260 265
- (2010) Catal. Lett. , vol.136 , pp. 260-265
- Shamin, T.¹ Paul, S.²

35
- 80055031952
- P. Veerakumar M. Velayudham K.-L. Lu S. Rajagopal Catal. Sci. Technol. 2011 1 1512 1525
- (2011) Catal. Sci. Technol. , vol.1 , pp. 1512-1525
- Veerakumar, P.¹ Velayudham, M.² Lu, K.-L.³ Rajagopal, S.⁴

36
- 77952776547
- B. S. Lee M. Yi S. Y. Chu J. Y. Lee R. Kwon K. R. Lee D. Kang W. S. Kim H. B. Lim J. Lee H.-J. Youn D. Y. Chi N. H. Hur Chem. Commun. 2010 46 3935 3937
- (2010) Chem. Commun. , vol.46 , pp. 3935-3937
- Lee, B.S.¹ Yi, M.² Chu, S.Y.³ Lee, J.Y.⁴ Kwon, R.⁵ Lee, K.R.⁶ Kang, D.⁷ Kim, W.S.⁸ Lim, H.B.⁹ Lee, J.¹⁰ Youn, H.-J.¹¹ Chi, D.Y.¹² Hur, N.H.¹³

37
- 38949181290
- I. S. Park M. S. Kwon Y. Kim J. S. Lee J. Park Org. Lett. 2008 10 497 500
- (2008) Org. Lett. , vol.10 , pp. 497-500
- Park, I.S.¹ Kwon, M.S.² Kim, Y.³ Lee, J.S.⁴ Park, J.⁵

38
- 61349130803
- T. Katayama K. Kamata K. Yamaguchi N. Mizuno ChemSusChem 2009 2 59 62
- (2009) ChemSusChem , vol.2 , pp. 59-62
- Katayama, T.¹ Kamata, K.² Yamaguchi, K.³ Mizuno, N.⁴

39
- 70349895735
- K. Yamaguchi T. Oishi T. Katayama N. Mizuno Chem.-Eur. J. 2009 15 10464 10472
- (2009) Chem.-Eur. J. , vol.15 , pp. 10464-10472
- Yamaguchi, K.¹ Oishi, T.² Katayama, T.³ Mizuno, N.⁴

40
- 62449182752
- K. Namitharan M. Kumarraja K. Pitchumani Chem.-Eur. J. 2009 15 2755 2758
- (2009) Chem.-Eur. J. , vol.15 , pp. 2755-2758
- Namitharan, K.¹ Kumarraja, M.² Pitchumani, K.³

41
- 62249208036
- H. Hagiwara H. Sasaki T. Hoshi T. Suzuki Synlett 2009 643 647
- (2009) Synlett , pp. 643-647
- Hagiwara, H.¹ Sasaki, H.² Hoshi, T.³ Suzuki, T.⁴

42
- 78549235418
- M. Lammens J. Skey S. Wallyn R. O'Reilly F. D. Prez Chem. Commun. 2010 46 8719 8721
- (2010) Chem. Commun. , vol.46 , pp. 8719-8721
- Lammens, M.¹ Skey, J.² Wallyn, S.³ O'Reilly, R.⁴ Prez, F.D.⁵

43
- 77954796069
- Z. Zhang C. Dong C. Yang D. Hu J. Long L. Wang H. Li Y. Chen D. Kong Adv. Synth. Catal. 2010 352 1600 1604
- (2010) Adv. Synth. Catal. , vol.352 , pp. 1600-1604
- Zhang, Z.¹ Dong, C.² Yang, C.³ Hu, D.⁴ Long, J.⁵ Wang, L.⁶ Li, H.⁷ Chen, Y.⁸ Kong, D.⁹

44
- 84861850402
- Y. M. A. Yamada S. M. Sarkar Y. Uozumi J. Am. Chem. Soc. 2012 134 9285 9290
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 9285-9290
- Yamada, Y.M.A.¹ Sarkar, S.M.² Uozumi, Y.³

45
- 84857519029
- T. Suzuka Y. Kawahara K. Ooshiro T. Nagamine K. Ogihara M. Higa Heterocycles 2012 85 615 626
- (2012) Heterocycles , vol.85 , pp. 615-626
- Suzuka, T.¹ Kawahara, Y.² Ooshiro, K.³ Nagamine, T.⁴ Ogihara, K.⁵ Higa, M.⁶

46
- 84860482181
- A. Kumar S. Aerry A. Saxena A. De S. Mozumdar Green Chem. 2012 14 1298 1301
- (2012) Green Chem. , vol.14 , pp. 1298-1301
- Kumar, A.¹ Aerry, S.² Saxena, A.³ De, A.⁴ Mozumdar, S.⁵

47
- 33646444425
- C. Girard E. Önen M. Aufort S. Beauvière E. Samson J. Herscovici Org. Lett. 2006 8 1689 1692
- (2006) Org. Lett. , vol.8 , pp. 1689-1692
- Girard, C.¹ Önen, E.² Aufort, M.³ Beauvière, S.⁴ Samson, E.⁵ Herscovici, J.⁶

48
- 59349112512
- I. Jlalia F. Meganem J. Herscovici C. Girard Molecules 2009 14 528 539
- (2009) Molecules , vol.14 , pp. 528-539
- Jlalia, I.¹ Meganem, F.² Herscovici, J.³ Girard, C.⁴

49
- 52949124445
- U. Sirion Y. J. Bae B. S. Lee D. Y. Chi Synlett 2008 2326 2330
- (2008) Synlett , pp. 2326-2330
- Sirion, U.¹ Bae, Y.J.² Lee, B.S.³ Chi, D.Y.⁴

50
- 0037168978
- For palladium on DIAION HP20, see
- T. Adachi S. Ando J. Watanabe J. Chromatogr., A 2002 944 41 59
- (2002) J. Chromatogr., A , vol.944 , pp. 41-59
- Adachi, T.¹ Ando, S.² Watanabe, J.³

51
- 58449124884
- Y. Monguchi Y. Fujita K. Endo S. Takao M. Yoshimura Y. Takagi T. Maegawa H. Sajiki Chem.-Eur. J. 2009 15 834 837
- (2009) Chem.-Eur. J. , vol.15 , pp. 834-837
- Monguchi, Y.¹ Fujita, Y.² Endo, K.³ Takao, S.⁴ Yoshimura, M.⁵ Takagi, Y.⁶ Maegawa, T.⁷ Sajiki, H.⁸

52
- 84859112331
- Y. Monguchi K. Sakai K. Endo Y. Fujita M. Niimura M. Yoshimura T. Mizusaki Y. Sawama H. Sajiki ChemCatChem 2012 4 546 558
- (2012) ChemCatChem , vol.4 , pp. 546-558
- Monguchi, Y.¹ Sakai, K.² Endo, K.³ Fujita, Y.⁴ Niimura, M.⁵ Yoshimura, M.⁶ Mizusaki, T.⁷ Sawama, Y.⁸ Sajiki, H.⁹

53
- 65549153031
- Y. Kitamura K. Taniguchi T. Maegawa Y. Monguchi Y. Kitade H. Sajiki Heterocycles 2009 77 521 532
- (2009) Heterocycles , vol.77 , pp. 521-532
- Kitamura, Y.¹ Taniguchi, K.² Maegawa, T.³ Monguchi, Y.⁴ Kitade, Y.⁵ Sajiki, H.⁶

54
- 84873290989
- Home page for DIAION of Mitsubishi Chemical Co.
- Home page for DIAION of Mitsubishi Chemical Co., see http://www.diaion. com/Index-E.htm

55
- 0033749878
- R. Koivula J. Lehto L. Pajo T. Gale H. Leinonen Hydrometallurgy 2000 56 93 108
- (2000) Hydrometallurgy , vol.56 , pp. 93-108
- Koivula, R.¹ Lehto, J.² Pajo, L.³ Gale, T.⁴ Leinonen, H.⁵

56
- 34248996225
- A. Cavaco S. Fernandes M. M. Quina L. M. Ferreira J. Hazard. Mater. 2007 144 634 638
- (2007) J. Hazard. Mater. , vol.144 , pp. 634-638
- Cavaco, A.¹ Fernandes, S.² Quina, M.M.³ Ferreira, L.M.⁴

57
- 67649743521
- S. A. Cavaco S. Fernandes C. M. Augusto M. J. Quina L. M. Gando-Ferreira J. Hazard. Mater. 2009 169 516 523
- (2009) J. Hazard. Mater. , vol.169 , pp. 516-523
- Cavaco, S.A.¹ Fernandes, S.² Augusto, C.M.³ Quina, M.J.⁴ Gando-Ferreira, L.M.⁵

58
- 79960976946
- The scanning transmission electron microscopy (STEM) images, electron probe microanalyses (EPMA), and X-ray photoelectron spectroscopy (XPS) spectra are shown in the supplementary data Although the copper-catalyzed homo-coupling (Glaser coupling) or/and polymerization of ethynylbenzene based on the acidic alkyne hydrogen strongly activated by the electron-withdrawing ester moiety might have taken place, the identification of each of the products was impossible because of the excessive complexity of the reaction
- L. M. Gando-Ferreira I. S. Romao M. J. Quina Chem. Eng. J. 2011 172 277 286
- (2011) Chem. Eng. J. , vol.172 , pp. 277-286
- Gando-Ferreira, L.M.¹ Romao, I.S.² Quina, M.J.³

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