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Tetrahedron Letters

Volumn 53, Issue 32, 2012, Pages 4199-4201

Enantioselective reductive aldol reaction using tertiary amine as hydride donor

(4) Osakama, Kazuki a Sugiura, Masaharu a Nakajima, Makoto a Kotani, Shunsuke a

a KUMAMOTO UNIVERSITY (Japan)

Author keywords

Aldol reaction; Asymmetric catalysis; Conjugate reduction; Phosphine oxide; Tertiary amine

Indexed keywords

CHALCONE DERIVATIVE; HYDROCHLORIC ACID; KETONE DERIVATIVE; LEWIS BASE; PHOSPHINE OXIDE DERIVATIVE; TERTIARY AMINE;

ALDOL REACTION; ARTICLE; CATALYST; ENANTIOSELECTIVITY; NUCLEAR OVERHAUSER EFFECT; REACTION TIME; STEREOCHEMISTRY;

EID: 84863613652 PISSN: 00404039 EISSN: 18733581 Source Type: Journal
DOI: 10.1016/j.tetlet.2012.05.147 Document Type: Article

Times cited : (28)

References (35)

1
- 33750995215
- For reviews on reductive aldol reaction, see: Angew. Chem., Int. Ed. 2006, 45, 354-366
- For reviews on reductive aldol reaction, see: H.-C. Guo, and J.-A. Ma Angew. Chem. 118 2006 362 375 Angew. Chem., Int. Ed. 2006, 45, 354-366
- (2006) Angew. Chem. , vol.118 , pp. 362-375
- Guo, H.-C.¹ Ma, J.-A.²

2
- 34347225080
- H. Nishiyama, and T. Shiomi Top. Curr. Chem. 279 2007 105 137
- (2007) Top. Curr. Chem. , vol.279 , pp. 105-137
- Nishiyama, H.¹ Shiomi, T.²

3
- 0034630894
- For enantioselective reductive aldol reaction, see
- For enantioselective reductive aldol reaction, see: S.J. Taylor, M.O. Duffey, and J.P. Morken J. Am. Chem. Soc. 122 2000 4528 4529
- (2000) J. Am. Chem. Soc. , vol.122 , pp. 4528-4529
- Taylor, S.J.¹ Duffey, M.O.² Morken, J.P.³

4
- 0001494417
- C.-X. Zhao, M.O. Duffey, S.J. Taylor, and J.P. Morken Org. Lett. 3 2001 1829 1831
- (2001) Org. Lett. , vol.3 , pp. 1829-1831
- Zhao, C.-X.¹ Duffey, M.O.² Taylor, S.J.³ Morken, J.P.⁴

5
- 3242725326
- A.E. Russell, N.O. Fuller, S.J. Taylor, P. Aurriset, and J.P. Morken Org. Lett. 6 2004 2309 2312
- (2004) Org. Lett. , vol.6 , pp. 2309-2312
- Russell, A.E.¹ Fuller, N.O.² Taylor, S.J.³ Aurriset, P.⁴ Morken, J.P.⁵

6
- 1842631430
- B.M. Bocknack, L.-C. Wang, and M. Krische J. Proc. Natl. Acad. Sci. 101 2004 5421 5424
- (2004) J. Proc. Natl. Acad. Sci. , vol.101 , pp. 5421-5424
- Bocknack, B.M.¹ Wang, L.-C.² Krische, M.³

7
- 18744395482
- H. Nishiyama, T. Shiomi, Y. Tsuchiya, and I. Matsuda J. Am. Chem. Soc. 127 2005 6972 6973
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 6972-6973
- Nishiyama, H.¹ Shiomi, T.² Tsuchiya, Y.³ Matsuda, I.⁴

8
- 20544434073
- N.O. Fuller, and J.P. Morken Synlett 2005 1459 1461
- (2005) Synlett , pp. 1459-1461
- Fuller, N.O.¹ Morken, J.P.²

9
- 25444446131
- H.W. Lam, and P.M. Joensuu Org. Lett. 7 2005 4225 4228
- (2005) Org. Lett. , vol.7 , pp. 4225-4228
- Lam, H.W.¹ Joensuu, P.M.²

10
- 33746247943
- Angew. Chem., Int. Ed., 2006, 45, 1292-1297
- J. Deschamp, O. Chuzel, J. Hannedouche, and O. Riant Angew. Chem. 118 2006 1314 1319 Angew. Chem., Int. Ed., 2006, 45, 1292-1297
- (2006) Angew. Chem. , vol.118 , pp. 1314-1319
- Deschamp, J.¹ Chuzel, O.² Hannedouche, J.³ Riant, O.⁴

11
- 31444451603
- D. Zhao, K. Oisaki, M. Kanai, and M. Shibasaki Tetrahedron Lett. 47 2006 1403 1407
- (2006) Tetrahedron Lett. , vol.47 , pp. 1403-1407
- Zhao, D.¹ Oisaki, K.² Kanai, M.³ Shibasaki, M.⁴

12
- 33750969372
- D. Zhao, K. Oisaki, M. Kanai, and M. Shibasaki J. Am. Chem. Soc. 128 2006 14440 14441
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 14440-14441
- Zhao, D.¹ Oisaki, K.² Kanai, M.³ Shibasaki, M.⁴

13
- 33846137282
- O. Chuzel, J. Deschamp, C. Chausteur, and O. Riant Org. Lett. 8 2006 5943 5946
- (2006) Org. Lett. , vol.8 , pp. 5943-5946
- Chuzel, O.¹ Deschamp, J.² Chausteur, C.³ Riant, O.⁴

14
- 33746763858
- J. Ito, T. Shiomi, and H. Nishiyama Adv. Synth. Catal. 348 2006 1235 1240
- (2006) Adv. Synth. Catal. , vol.348 , pp. 1235-1240
- Ito, J.¹ Shiomi, T.² Nishiyama, H.³

15
- 33845936678
- T. Shiomi, J. Ito, Y. Yamamoto, and H. Nishiyama Eur. J. Org. Chem. 2006 5594 5600
- (2006) Eur. J. Org. Chem. , pp. 5594-5600
- Shiomi, T.¹ Ito, J.² Yamamoto, Y.³ Nishiyama, H.⁴

16
- 34248360397
- T. Shiomi, and H. Nishiyama Org. Lett. 9 2007 1651 1654
- (2007) Org. Lett. , vol.9 , pp. 1651-1654
- Shiomi, T.¹ Nishiyama, H.²

17
- 40949114623
- C. Bee, S.B. Han, A. Hassan, H. Iida, and M.J. Krische J. Am. Chem. Soc. 130 2008 2746 2747
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 2746-2747
- Bee, C.¹ Han, S.B.² Hassan, A.³ Iida, H.⁴ Krische, M.J.⁵

18
- 55549102693
- B.H. Lipshutz, B. Amorelli, and J.B. Unger J. Am. Chem. Soc. 130 2008 14378 14379
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 14378-14379
- Lipshutz, B.H.¹ Amorelli, B.² Unger, J.B.³

19
- 64349119751
- T. Shiomi, T. Adachi, J. Ito, and H. Nishiyama Org. Lett. 11 2009 1011 1014
- (2009) Org. Lett. , vol.11 , pp. 1011-1014
- Shiomi, T.¹ Adachi, T.² Ito, J.³ Nishiyama, H.⁴

20
- 64049112847
- J. Deschamp, and O. Riant Org. Lett. 11 2009 1217 1220
- (2009) Org. Lett. , vol.11 , pp. 1217-1220
- Deschamp, J.¹ Riant, O.²

21
- 67649442807
- M. Kato, H. Oki, K. Ogata, and S. Fukuzawa Synlett 2009 1299 1302
- (2009) Synlett , pp. 1299-1302
- Kato, M.¹ Oki, H.² Ogata, K.³ Fukuzawa, S.⁴

22
- 52649107590
- M. Sugiura, N. Sato, S. Kotani, and M. Nakajima Chem. Commun. 2008 4309 4311
- (2008) Chem. Commun. , pp. 4309-4311
- Sugiura, M.¹ Sato, N.² Kotani, S.³ Nakajima, M.⁴

23
- 77749296044
- M. Sugiura, N. Sato, Y. Sonoda, S. Kotani, and M. Nakajima Chem. Asian J. 5 2010 478 481
- (2010) Chem. Asian J. , vol.5 , pp. 478-481
- Sugiura, M.¹ Sato, N.² Sonoda, Y.³ Kotani, S.⁴ Nakajima, M.⁵

24
- 79961067087
- S. Kotani, K. Osakama, M. Sugiura, and M. Nakajima Org. Lett. 13 2011 3968 3971
- (2011) Org. Lett. , vol.13 , pp. 3968-3971
- Kotani, S.¹ Osakama, K.² Sugiura, M.³ Nakajima, M.⁴

25
- 54749122929
- For reviews on Lewis base organocatalysts, see: Angew. Chem., Int. Ed. 2008, 47, 1560-1638
- For reviews on Lewis base organocatalysts, see: S.E. Denmark, and G.L. Beutner Angew. Chem. 120 2008 1584 1663 Angew. Chem., Int. Ed. 2008, 47, 1560-1638
- (2008) Angew. Chem. , vol.120 , pp. 1584-1663
- Denmark, S.E.¹ Beutner, G.L.²

26
- 33646555477
- Y. Orito, and M. Nakajima Synthesis 2006 1391 1401
- (2006) Synthesis , pp. 1391-1401
- Orito, Y.¹ Nakajima, M.²

27
- 33846104288
- A.V. Malkov, and P. Kočovský Eur. J. Org. Chem. 2007 29 36
- (2007) Eur. J. Org. Chem. , pp. 29-36
- Malkov, A.V.¹ Kočovský, P.²

28
- 77955502679
- M. Benaglia, and S. Rossi Org. Biomol. Chem. 8 2010 3824 3830
- (2010) Org. Biomol. Chem. , vol.8 , pp. 3824-3830
- Benaglia, M.¹ Rossi, S.²

29
- 33646557046
- For phosphine oxide-catalyzed enantioselective aldol reactions, see
- For phosphine oxide-catalyzed enantioselective aldol reactions, see: S. Kotani, S. Hashimoto, and M. Nakajima Synlett 2006 1116 1118
- (2006) Synlett , pp. 1116-1118
- Kotani, S.¹ Hashimoto, S.² Nakajima, M.³

30
- 33847632961
- S. Kotani, S. Hashimoto, and M. Nakajima Tetrahedron 63 2007 3122 3132
- (2007) Tetrahedron , vol.63 , pp. 3122-3132
- Kotani, S.¹ Hashimoto, S.² Nakajima, M.³

31
- 67449088256
- S. Kotani, Y. Shimoda, M. Sugiura, and M. Nakajima Tetrahedron Lett. 50 2009 4602 4605
- (2009) Tetrahedron Lett. , vol.50 , pp. 4602-4605
- Kotani, S.¹ Shimoda, Y.² Sugiura, M.³ Nakajima, M.⁴

32
- 79955560732
- S. Kotani, S. Aoki, M. Sugiura, and M. Nakajima Tetrahedron Lett. 52 2011 2834 2836
- (2011) Tetrahedron Lett. , vol.52 , pp. 2834-2836
- Kotani, S.¹ Aoki, S.² Sugiura, M.³ Nakajima, M.⁴

33
- 78649790892
- S. Rossi, M. Benaglia, A. Genoni, T. Benincori, and G. Celentano Tetrahedron 67 2011 158 166
- (2011) Tetrahedron , vol.67 , pp. 158-166
- Rossi, S.¹ Benaglia, M.² Genoni, A.³ Benincori, T.⁴ Celentano, G.⁵

34
- 79955378501
- S. Rossi, M. Benaglia, F. Cozzi, A. Genoni, and T. Benincori Adv. Synth. Catal. 353 2011 848 854
- (2011) Adv. Synth. Catal. , vol.353 , pp. 848-854
- Rossi, S.¹ Benaglia, M.² Cozzi, F.³ Genoni, A.⁴ Benincori, T.⁵

35
- 0037073229
- Low reactivity of non-conjugated aldehydes has been observed for Lewis base-catalyzed reactions with trichlorosilylated reagents due to the formation of the corresponding O-silylated chlorohydrins, see
- Low reactivity of non-conjugated aldehydes has been observed for Lewis base-catalyzed reactions with trichlorosilylated reagents due to the formation of the corresponding O-silylated chlorohydrins, see: S.E. Denmark, T. Wynn, and G.L. Beutner J. Am. Chem. Soc. 124 2002 13405 13407
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 13405-13407
- Denmark, S.E.¹ Wynn, T.² Beutner, G.L.³

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