SCOPUS 정보 검색 플랫폼

Organic and Biomolecular Chemistry

Volumn 11, Issue 27, 2013, Pages 4429-4432

Tandem nucleophilic addition-Oppenauer oxidation of aromatic aldehydes to aryl ketones with triorganoaluminium reagents

(7) Fu, Ying a Yang, Yanshou a Hügel, Helmut M b Du, Zhengyin a Wang, Kehu a Huang, Danfeng a Hu, Yulai a

a NORTHWEST NORMAL UNIVERSITY (China)

b RMIT UNIVERSITY (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; AROMATIC COMPOUNDS; KETONES;

AROMATIC ALDEHYDE; ARYL KETONES; HIGH YIELD; PINACOLONE;

ALDEHYDES;

EID: 84881047809 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c3ob40642c Document Type: Article

Times cited : (18)

References (35)

1
- 84863337931
- Y. Shen C.-F. Chen Chem. Rev. 2012 112 1463 1535
- (2012) Chem. Rev. , vol.112 , pp. 1463-1535
- Shen, Y.¹ Chen, C.-F.²

2
- 3543059896
- M. Chrzanowska M. D. Rozwadowska Chem. Rev. 2004 104 3341 3370
- (2004) Chem. Rev. , vol.104 , pp. 3341-3370
- Chrzanowska, M.¹ Rozwadowska, M.D.²

3
- 84869193062
- Y.-B. Wu Z.-Y. Ni Q.-W. Shi M. Dong H. Kiyota Y.-C. Gu B. Cong Chem. Rev. 2012 112 5967 6026
- (2012) Chem. Rev. , vol.112 , pp. 5967-6026
- Wu, Y.-B.¹ Ni, Z.-Y.² Shi, Q.-W.³ Dong, M.⁴ Kiyota, H.⁵ Gu, Y.-C.⁶ Cong, B.⁷

4
- 0003729256
- Marcel Dekker, New York
- R. M. Roberts and A. A. Khalaf, Friedel-Crafts Alkylation Chemistry. A Century of Discovery, Marcel Dekker, New York, 1984
- (1984) Friedel-Crafts Alkylation Chemistry. A Century of Discovery
- Roberts, R.M.¹ Khalaf, A.A.²

5
- 33845207951
- A. Takemiya J. F. Hartwig J. Am. Chem. Soc. 2006 128 14800 14801
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 14800-14801
- Takemiya, A.¹ Hartwig, J.F.²

6
- 49449117421
- J. Ruan O. Saidi J. A. Iggo J. Xiao J. Am. Chem. Soc. 2008 130 10510 10511
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 10510-10511
- Ruan, J.¹ Saidi, O.² Iggo, J.A.³ Xiao, J.⁴

7
- 0037040709
- Y.-C. Huang K. K. Majumdar C.-H. Cheng J. Org. Chem. 2002 67 1682 1684
- (2002) J. Org. Chem. , vol.67 , pp. 1682-1684
- Huang, Y.-C.¹ Majumdar, K.K.² Cheng, C.-H.³

8
- 77955708083
- P. Colbon J. Ruan M. Purdie J. Xiao Org. Lett. 2010 12 3670 3673
- (2010) Org. Lett. , vol.12 , pp. 3670-3673
- Colbon, P.¹ Ruan, J.² Purdie, M.³ Xiao, J.⁴

9
- 12344337684
- S. Ko B. Kang S. Chang Angew. Chem., Int. Ed. 2005 44 455 457
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 455-457
- Ko, S.¹ Kang, B.² Chang, S.³

10
- 38949166785
- C. Qin J. Chen H. Wua J. Cheng Q. Zhang B. Zuo W. Su J. Ding Tetrahedron Lett. 2008 49 1884 1888
- (2008) Tetrahedron Lett. , vol.49 , pp. 1884-1888
- Qin, C.¹ Chen, J.² Wua, H.³ Cheng, J.⁴ Zhang, Q.⁵ Zuo, B.⁶ Su, W.⁷ Ding, J.⁸

11
- 77349099246
- M. C. Willis Chem. Rev. 2010 110 725 748
- (2010) Chem. Rev. , vol.110 , pp. 725-748
- Willis, M.C.¹

12
- 84863451341
- S. R. Neufeldt M. S. Sanford Acc. Chem. Res. 2012 45 936 946
- (2012) Acc. Chem. Res. , vol.45 , pp. 936-946
- Neufeldt, S.R.¹ Sanford, M.S.²

13
- 67650283702
- X. Jia S. Zhang W. Wang F. Luo J. Cheng Org. Lett. 2009 11 3120 3123
- (2009) Org. Lett. , vol.11 , pp. 3120-3123
- Jia, X.¹ Zhang, S.² Wang, W.³ Luo, F.⁴ Cheng, J.⁵

14
- 77956204996
- C.-W. Chan Z. Zhou A. S. C. Chan W.-Y. Yu Org. Lett. 2010 12 3926 3929
- (2010) Org. Lett. , vol.12 , pp. 3926-3929
- Chan, C.-W.¹ Zhou, Z.² Chan, A.S.C.³ Yu, W.-Y.⁴

15
- 33845932176
- R. J. Kloetzing A. Krasovskiy P. Knochel Chem.-Eur. J. 2007 13 215 227
- (2007) Chem.-Eur. J. , vol.13 , pp. 215-227
- Kloetzing, R.J.¹ Krasovskiy, A.² Knochel, P.³

16
- 0008498578
- B. Byrne M. Karras Tetrahedron Lett. 1987 28 769 772
- (1987) Tetrahedron Lett. , vol.28 , pp. 769-772
- Byrne, B.¹ Karras, M.²

17
- 0032355222
- B. K. Wilk J. L. Helom C. W. Coughlin Org. Process Res. Dev. 1998 2 407 411
- (1998) Org. Process Res. Dev. , vol.2 , pp. 407-411
- Wilk, B.K.¹ Helom, J.L.² Coughlin, C.W.³

18
- 23844501944
- M. Schroeter Synth. Commun. 2005 35 2203 2212
- (2005) Synth. Commun. , vol.35 , pp. 2203-2212
- Schroeter, M.¹

19
- 0001143623
- J. L. Namy J. Souppe J. Collin H. B. Kagan J. Org. Chem. 1984 49 2045 2049
- (1984) J. Org. Chem. , vol.49 , pp. 2045-2049
- Namy, J.L.¹ Souppe, J.² Collin, J.³ Kagan, H.B.⁴

20
- 0001281205
- B. Zheng M. Srebnik J. Org. Chem. 1995 60 3278 3279
- (1995) J. Org. Chem. , vol.60 , pp. 3278-3279
- Zheng, B.¹ Srebnik, M.²

21
- 0037023457
- H. S. Schrekker M. W. G. de Bolster R. V. A. Orru L. A. Wessjohann J. Org. Chem. 2002 67 1975 1981
- (2002) J. Org. Chem. , vol.67 , pp. 1975-1981
- Schrekker, H.S.¹ De Bolster, M.W.G.² Orru, R.V.A.³ Wessjohann, L.A.⁴

22
- 9644295537
- M. Pucheault S. Darses J.-P. Genet J. Am. Chem. Soc. 2004 126 15356 15357
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 15356-15357
- Pucheault, M.¹ Darses, S.² Genet, J.-P.³

23
- 0037454983
- J. Augé N. Lubin-Germain L. Seghrouchni Tetrahedron Lett. 2003 44 819 821
- (2003) Tetrahedron Lett. , vol.44 , pp. 819-821
- Augé, J.¹ Lubin-Germain, N.² Seghrouchni, L.³

24
- 0037158196
- J. Augé N. Lubin-Germain L. Seghrouchni Tetrahedron Lett. 2002 43 5255 5256
- (2002) Tetrahedron Lett. , vol.43 , pp. 5255-5256
- Augé, J.¹ Lubin-Germain, N.² Seghrouchni, L.³

25
- 84874877674
- Angew. Chem., Int. Ed. 2002 41 2757 2760
- J.-X. Wang Y. Fu Y. L. Hu Angew. Chem. 2002 114 2881 2884 Angew. Chem., Int. Ed. 2002 41 2757 2760
- (2002) Angew. Chem. , vol.114 , pp. 2881-2884
- Wang, J.-X.¹ Fu, Y.² Hu, Y.L.³

26
- 0043245936
- J.-X. Wang Y. Fu Y. L. Hu Synthesis 2003 1506 1510
- (2003) Synthesis , pp. 1506-1510
- Wang, J.-X.¹ Fu, Y.² Hu, Y.L.³

27
- 84862804732
- Y. Fu X. Hu Y. Chen Y. Yang H. Hou Y. Hu Synthesis 2012 1030 1036
- (2012) Synthesis , pp. 1030-1036
- Fu, Y.¹ Hu, X.² Chen, Y.³ Yang, Y.⁴ Hou, H.⁵ Hu, Y.⁶

28
- 54549092399
- Y. Fu J.-X. Wang K. Wang Y. Hu Tetrahedron 2008 64 11124 11128
- (2008) Tetrahedron , vol.64 , pp. 11124-11128
- Fu, Y.¹ Wang, J.-X.² Wang, K.³ Hu, Y.⁴

29
- 84874819172
- Y. Fu Y. Liu Y. Chen H. M. Hügel M. Wang D. Huang Y. Hu Org. Biomol. Chem. 2012 10 7669 7672
- (2012) Org. Biomol. Chem. , vol.10 , pp. 7669-7672
- Fu, Y.¹ Liu, Y.² Chen, Y.³ Hügel, H.M.⁴ Wang, M.⁵ Huang, D.⁶ Hu, Y.⁷

30
- 69549114759
- Z.-Y. Peng F.-F. Ma L.-F. Zhu X.-M. Xie Z. Zhang J. Org. Chem. 2009 74 6855 6858
- (2009) J. Org. Chem. , vol.74 , pp. 6855-6858
- Peng, Z.-Y.¹ Ma, F.-F.² Zhu, L.-F.³ Xie, X.-M.⁴ Zhang, Z.⁵

31
- 0025021044
- M. B. Power A. R. Barron Tetrahedron Lett. 1990 31 323 324
- (1990) Tetrahedron Lett. , vol.31 , pp. 323-324
- Power, M.B.¹ Barron, A.R.²

32
- 0001278542
- C. Djerassi Org. React. 1951 VI 207 272
- (1951) Org. React. , vol.6 , pp. 207-272
- Djerassi, C.¹

33
- 0027943932
- C. F. de Graauw J. A. Peters H. van Bekkum J. Huskens Synthesis 1994 1007 1017
- (1994) Synthesis , pp. 1007-1017
- De Graauw, C.F.¹ Peters, J.A.² Van Bekkum, H.³ Huskens, J.⁴

34
- 0037458962
- T. Suzuki K. Morita M. Tsuchida K. Hiroi J. Org. Chem. 2003 68 1601 1602
- (2003) J. Org. Chem. , vol.68 , pp. 1601-1602
- Suzuki, T.¹ Morita, K.² Tsuchida, M.³ Hiroi, K.⁴

35
- 55749110750
- C.-R. Chen H.-M. Gau Acta Crystallogr., Sect. E: Struct. Rep. Online 2008 64 m1381
- (2008) Acta Crystallogr., Sect. E: Struct. Rep. Online , vol.64 , pp. 1381
- Chen, C.-R.¹ Gau, H.-M.²

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