SCOPUS 정보 검색 플랫폼

European Journal of Organic Chemistry

Volumn 2015, Issue 24, 2015, Pages 5293-5303

Substrate Activation in the Catalytic Asymmetric Hydrogenation of N-Heteroarenes

(3) Balakrishna, Bugga a Núñez Rico, José Luis a Vidal Ferran, Anton a,b

a INSTITUTE OF CHEMICAL RESEARCH OF CATALONIA ICIQ (Spain)

b INSTITUCIÓ CATALANA DE RECERCA I ESTUDIS AVANÇATS ICREA (Spain)

Author keywords

Asymmetric catalysis; Enantioselectivity; Hydrogenation; Iridium; Nitrogen heterocycles; Palladium

Indexed keywords

EID: 84939272027 PISSN: 1434193X EISSN: 10990690 Source Type: Journal
DOI: 10.1002/ejoc.201500588 Document Type: Review

Times cited : (57)

References (87)

1
- 84939294471
- Biological Significance - Pharmacology, Pharmaceutical Agrochemical in Comprehensive Chirality, 1 (Eds.:, Elsevier, Oxford, UK
- Biological Significance-Pharmacology, Pharmaceutical Agrochemical in Comprehensive Chirality, vol. 1 (Eds.:, E. M. Carreira, H. Yamamoto), Elsevier, Oxford, UK, 2012.
- (2012)
- Carreira, E.M.¹ Yamamoto, H.²

2
- 0003400107
- Wiley, New York, USA
- R. Noyori, in: Asymmetric Catalysis in Organic Synthesis Wiley, New York, USA, 1994.
- (1994) Asymmetric Catalysis in Organic Synthesis
- Noyori, R.¹

3
- 0003889420
- Wiley, New York, USA
- G. Q. Lin, Y. M. Li, A. S. C. Chan, in: Principles and Applications of Asymmetric Synthesis Wiley, New York, USA, 2001.
- (2001) Principles and Applications of Asymmetric Synthesis
- Lin, G.Q.¹ Li, Y.M.² Chan, A.S.C.³

4
- 84939294472
- Comprehensive Asymmetric Catalysis (Eds.:, Springer-Verlag, Heidelberg, Germany
- Comprehensive Asymmetric Catalysis (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer-Verlag, Heidelberg, Germany, 2012.
- (2012)
- Jacobsen, E.N.¹ Pfaltz, A.² Yamamoto, H.³

5
- 84902422003
- Comprehensive Chirality, Vols. 1-9 (Eds.:, Elsevier, Oxford, UK
- Comprehensive Chirality, Vols. 1-9 (Eds.:, E. M. Carreira, H. Yamamoto), Elsevier, Oxford, UK, 2012.
- (2012)
- Carreira, E.M.¹ Yamamoto, H.²

6
- 84939294474
- Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions (Eds.:, Wiley-VCH, Weinheim, Germany
- Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions (Eds.:, H.-U. Blaser, E. Schmidt), Wiley-VCH, Weinheim, Germany, 2004.
- (2004)
- Blaser, H.-U.¹ Schmidt, E.²

7
- 38049036296
- H.-U. Blaser, B. Pugin, F. Spindler, M. Thommen, Acc. Chem. Res. 2007, 40, 1240-1250.
- (2007) Acc. Chem. Res. , vol.40 , pp. 1240-1250
- Blaser, H.-U.¹ Pugin, B.² Spindler, F.³ Thommen, M.⁴

8
- 84891569347
- Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions, 2nd ed. (Eds.:, Wiley-VCH, Weinheim, Germany
- Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions, 2nd ed. (Eds.:, H.-U. Blaser, H.-J. Federsel), Wiley-VCH, Weinheim, Germany, 2010.
- (2010)
- Blaser, H.-U.¹ Federsel, H.-J.²

9
- 84890985460
- Handbook of Homogeneous Hydrogenation (Eds.:, Wiley-VCH, Weinheim, Germany
- Handbook of Homogeneous Hydrogenation (Eds.:, J. G. de Vries, C. J. Elsevier), Wiley-VCH, Weinheim, Germany, 2004.
- (2004)
- De Vries, J.G.¹ Elsevier, C.J.²

10
- 84867050896
- in:, in: Organometallics as Catalysts in the Fine Chemical Industry (Eds.:, Springer-Verlag, Berlin/Heidelberg, Germany
- H.-U. Blaser, B. Pugin, F. Spindler, in: Asymmetric Hydrogenation, in: Organometallics as Catalysts in the Fine Chemical Industry (Eds.:, M. Beller, H.-U. Blaser), Springer-Verlag, Berlin/Heidelberg, Germany, 2012.
- (2012) Asymmetric Hydrogenation
- Blaser, H.-U.¹ Pugin, B.² Spindler, F.³ Beller, M.⁴ Blaser, H.-U.⁵

11
- 84871973622
- P. Etayo, A. Vidal-Ferran, Chem. Soc. Rev. 2013, 42, 728-754.
- (2013) Chem. Soc. Rev. , vol.42 , pp. 728-754
- Etayo, P.¹ Vidal-Ferran, A.²

12
- 84884678435
- A. Cadu, P. G. Andersson, Dalton Trans. 2013, 42, 14345-14356.
- (2013) Dalton Trans. , vol.42 , pp. 14345-14356
- Cadu, A.¹ Andersson, P.G.²

13
- 84878221209
- A. Bartoszewicz, N. Ahlsten, B. Martín-Matute, Chem. Eur. J. 2013, 19, 7274-7302.
- (2013) Chem. Eur. J. , vol.19 , pp. 7274-7302
- Bartoszewicz, A.¹ Ahlsten, N.² Martín-Matute, B.³

14
- 84939294478
- Phosphorus Ligands in Asymmetric Catalysis, 1st ed. (Ed.:, Wiley-VCH, Weinheim, Germany, Vols. I-III
- Phosphorus Ligands in Asymmetric Catalysis, 1st ed. (Ed.:, A. Börner), Wiley-VCH, Weinheim, Germany, 2008; Vols. I-III.
- (2008)
- Börner, A.¹

15
- 79952679097
- H. Fernández-Pérez, P. Etayo, A. Panossian, A. Vidal-Ferran, Chem. Rev. 2011, 111, 2119-2176.
- (2011) Chem. Rev. , vol.111 , pp. 2119-2176
- Fernández-Pérez, H.¹ Etayo, P.² Panossian, A.³ Vidal-Ferran, A.⁴

16
- 84922126920
- For selected references on the asymmetric hydrogenation of C=C bonds, see
- J.-H. Xie, D.-H. Bao, Q.-L. Zhou, Synthesis 2015, 47, 460-471. For selected references on the asymmetric hydrogenation of C=C bonds, see
- (2015) Synthesis , vol.47 , pp. 460-471
- Xie, J.-H.¹ Bao, D.-H.² Zhou, Q.-L.³

17
- 38049078593
- S. J. Roseblade, A. Pfaltz, Acc. Chem. Res. 2007, 40, 1402-1411.
- (2007) Acc. Chem. Res. , vol.40 , pp. 1402-1411
- Roseblade, S.J.¹ Pfaltz, A.²

18
- 39649118398
- T. L. Church, P. G. Andersson, Coord. Chem. Rev. 2008, 252, 513-531.
- (2008) Coord. Chem. Rev. , vol.252 , pp. 513-531
- Church, T.L.¹ Andersson, P.G.²

19
- 79952684475
- J.-H. Xie, S.-F. Zhu, Q.-L. Zhou, Chem. Rev. 2011, 111, 1713-1760.
- (2011) Chem. Rev. , vol.111 , pp. 1713-1760
- Xie, J.-H.¹ Zhu, S.-F.² Zhou, Q.-L.³

20
- 79959865225
- For selected references on the asymmetric hydrogenation of C=N bonds, see ref.^[6e] and the following
- D. H. Woodmansee, A. Pfaltz, Chem. Commun. 2011, 47, 7912-7916. For selected references on the asymmetric hydrogenation of C=N bonds, see ref.^[6e] and the following
- (2011) Chem. Commun. , vol.47 , pp. 7912-7916
- Woodmansee, D.H.¹ Pfaltz, A.²

21
- 78650674643
- N. Fleury-Brégeot, V. de la Fuente, S. Castillõn, C. Claver, ChemCatChem 2010, 2, 1346-1371.
- (2010) ChemCatChem , vol.2 , pp. 1346-1371
- Fleury-Brégeot, N.¹ De La Fuente, V.² Castillõn, S.³ Claver, C.⁴

22
- 80052091185
- C. Wang, B. Villa-Marcos, J. Xiao, Chem. Commun. 2011, 47, 9773-9785.
- (2011) Chem. Commun. , vol.47 , pp. 9773-9785
- Wang, C.¹ Villa-Marcos, B.² Xiao, J.³

23
- 84894373197
- K. H. Hopmann, A. Bayer, Coord. Chem. Rev. 2014, 268, 59-82.
- (2014) Coord. Chem. Rev. , vol.268 , pp. 59-82
- Hopmann, K.H.¹ Bayer, A.²

24
- 0031449261
- J. P. Michael, Nat. Prod. Rep. 1997, 14, 605-618.
- (1997) Nat. Prod. Rep. , vol.14 , pp. 605-618
- Michael, J.P.¹

25
- 0031931850
- J. W. Daly, J. Nat. Prod. 1998, 61, 162-172.
- (1998) J. Nat. Prod. , vol.61 , pp. 162-172
- Daly, J.W.¹

26
- 0033775563
- D. O'Hagan, Nat. Prod. Rep. 2000, 17, 435-446.
- (2000) Nat. Prod. Rep. , vol.17 , pp. 435-446
- O'Hagan, D.¹

27
- 27844526992
- J. W. Daly, T. F. Spande, H. M. Garraffo, J. Nat. Prod. 2005, 68, 1556-1575.
- (2005) J. Nat. Prod. , vol.68 , pp. 1556-1575
- Daly, J.W.¹ Spande, T.F.² Garraffo, H.M.³

28
- 26844582966
- J. P. Michael, Nat. Prod. Rep. 2005, 22, 603-626.
- (2005) Nat. Prod. Rep. , vol.22 , pp. 603-626
- Michael, J.P.¹

29
- 84939294479
- Pharmaceutical Substances, 5th ed. (Eds.:, Georg Thieme, Stuttgart, Germany
- Pharmaceutical Substances, 5th ed. (Eds.:, A. Kleemann, J. Engel, B. Kutscher, D. Reichert), Georg Thieme, Stuttgart, Germany, 2008.
- (2008)
- Kleemann, A.¹ Engel, J.² Kutscher, B.³ Reichert, D.⁴

30
- 80051545932
- S. Samwel, J. O. Odalo, M. H. H. Nkunya, C. C. Joseph, N. A. Koorbanally, Phytochemistry 2011, 72, 1826-1832.
- (2011) Phytochemistry , vol.72 , pp. 1826-1832
- Samwel, S.¹ Odalo, J.O.² Nkunya, M.H.H.³ Joseph, C.C.⁴ Koorbanally, N.A.⁵

31
- 29144521717
- F. Glorius, Org. Biomol. Chem. 2005, 3, 4171-4175.
- (2005) Org. Biomol. Chem. , vol.3 , pp. 4171-4175
- Glorius, F.¹

32
- 38049066005
- Y.-G. Zhou, Acc. Chem. Res. 2007, 40, 1357-1366.
- (2007) Acc. Chem. Res. , vol.40 , pp. 1357-1366
- Zhou, Y.-G.¹

33
- 61349102524
- R. Kuwano, Heterocycles 2008, 76, 909-922.
- (2008) Heterocycles , vol.76 , pp. 909-922
- Kuwano, R.¹

34
- 84856417672
- D.-S. Wang, Q.-A. Chen, S.-M. Lu, Y.-G. Zhou, Chem. Rev. 2012, 112, 2557-2590.
- (2012) Chem. Rev. , vol.112 , pp. 2557-2590
- Wang, D.-S.¹ Chen, Q.-A.² Lu, S.-M.³ Zhou, Y.-G.⁴

35
- 84871993508
- Q.-A. Chen, Z.-S. Ye, Y. Duan, Y.-G. Zhou, Chem. Soc. Rev. 2013, 42, 497-511.
- (2013) Chem. Soc. Rev. , vol.42 , pp. 497-511
- Chen, Q.-A.¹ Ye, Z.-S.² Duan, Y.³ Zhou, Y.-G.⁴

36
- 84899566287
- in:, in: Stereoselective Formation of Amines, Topics in Current Chemistry, 343 (Eds.:, Springer-Verlag, Berlin/Heidelberg, Germany, p. 145-190
- Y.-M. He, F.-T. Song, Q.-H. Fan, in: Advances in Transition Metal-Catalyzed Asymmetric Hydrogenation of Heteroaromatic Compounds, in: Stereoselective Formation of Amines, Topics in Current Chemistry, 343 (Eds.:, W. Li, X. Zhang), Springer-Verlag, Berlin/Heidelberg, Germany, 2014, p. 145-190.
- (2014) Advances in Transition Metal-Catalyzed Asymmetric Hydrogenation of Heteroaromatic Compounds
- He, Y.-M.¹ Song, F.-T.² Fan, Q.-H.³ Li, W.⁴ Zhang, X.⁵

37
- 0001213784
- J. M. Brown, P. A. Chaloner, J. Am. Chem. Soc. 1980, 102, 3040-3048.
- (1980) J. Am. Chem. Soc. , vol.102 , pp. 3040-3048
- Brown, J.M.¹ Chaloner, P.A.²

38
- 33845281011
- C. R. Landis, J. Halpern, J. Am. Chem. Soc. 1987, 109, 1746-1754.
- (1987) J. Am. Chem. Soc. , vol.109 , pp. 1746-1754
- Landis, C.R.¹ Halpern, J.²

39
- 79955587229
- M. Rueping, J. Dufour, F. R. Schoepke, Green Chem. 2011, 13, 1084-1105.
- (2011) Green Chem. , vol.13 , pp. 1084-1105
- Rueping, M.¹ Dufour, J.² Schoepke, F.R.³

40
- 84939294481
- For previous reviews on substrate activation, see ref.^[8b] and
- For previous reviews on substrate activation, see ref.^[8b] and

41
- 84862666912
- Angew. Chem. 2012, 124, 6164
- Z. Yu, W. Jin, Q. Jiang, Angew. Chem. Int. Ed. 2012, 51, 6060-6072; Angew. Chem. 2012, 124, 6164.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 6060-6072
- Yu, Z.¹ Jin, W.² Jiang, Q.³

42
- 84890912060
- T. Nagano, A. Iimuro, K. Yamaji, Y. Kita, K. Mashima, Heterocycles 2014, 88, 103-127.
- (2014) Heterocycles , vol.88 , pp. 103-127
- Nagano, T.¹ Iimuro, A.² Yamaji, K.³ Kita, Y.⁴ Mashima, K.⁵

43
- 79959493473
- T. Wang, L.-G. Zhuo, Z. Li, F. Chen, Z. Ding, Y. He, Q.-H. Fan, J. Xiang, Z.-X. Yu, A. S. C. Chan, J. Am. Chem. Soc. 2011, 133, 9878-9891.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 9878-9891
- Wang, T.¹ Zhuo, L.-G.² Li, Z.³ Chen, F.⁴ Ding, Z.⁵ He, Y.⁶ Fan, Q.-H.⁷ Xiang, J.⁸ Yu, Z.-X.⁹ Chan, A.S.C.¹⁰

44
- 79955888743
- G. E. Dobereiner, A. Nova, N. D. Schley, N. Hazari, S. J. Miller, O. Eisenstein, R. H. Crabtree, J. Am. Chem. Soc. 2011, 133, 7547-7562.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 7547-7562
- Dobereiner, G.E.¹ Nova, A.² Schley, N.D.³ Hazari, N.⁴ Miller, S.J.⁵ Eisenstein, O.⁶ Crabtree, R.H.⁷

45
- 70349653339
- H. Tadaoka, D. Cartigny, T. Nagano, T. Gosavi, T. Ayad, J.-P. Genêt, T. Ohshima, V. Ratovelomanana-Vidal, K. Mashima, Chem. Eur. J. 2009, 15, 9990-9994.
- (2009) Chem. Eur. J. , vol.15 , pp. 9990-9994
- Tadaoka, H.¹ Cartigny, D.² Nagano, T.³ Gosavi, T.⁴ Ayad, T.⁵ Genêt, J.-P.⁶ Ohshima, T.⁷ Ratovelomanana-Vidal, V.⁸ Mashima, K.⁹

46
- 54249139518
- Seminal examples of activation of quinoline-type substrates by acids were reported by Chan, Fan, and co-workers (see ref.^[12a] and Angew. Chem. 2008, 120, 8592). However, because these examples involve the use of stoichiometric amounts of metal catalysts they have not been summarized in this microreview, which deals with catalytic methods
- Seminal examples of activation of quinoline-type substrates by acids were reported by Chan, Fan, and co-workers (see ref.^[12a] and: H. Zhou, Z. Li, Z. Wang, T. Wang, L. Xu, Y. He, Q.-H. Fan, J. Pan, L. Gu, A. S. C. Chan, Angew. Chem. Int. Ed. 2008, 47, 8464-8467; Angew. Chem. 2008, 120, 8592). However, because these examples involve the use of stoichiometric amounts of metal catalysts they have not been summarized in this microreview, which deals with catalytic methods.
- (2008) Angew Chem. Int. Ed. , vol.47 , pp. 8464-8467
- Zhou, H.¹ Li, Z.² Wang, Z.³ Wang, T.⁴ Xu, L.⁵ He, Y.⁶ Fan, Q.-H.⁷ Pan, J.⁸ Gu, L.⁹ Chan, A.S.C.¹⁰

47
- 84873531052
- Angew. Chem. 2013, 125, 2100
- A. Iimuro, K. Yamaji, S. Kandula, T. Nagano, Y. Kita, K. Mashima, Angew. Chem. Int. Ed. 2013, 52, 2046-2050; Angew. Chem. 2013, 125, 2100.
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 2046-2050
- Iimuro, A.¹ Yamaji, K.² Kandula, S.³ Nagano, T.⁴ Kita, Y.⁵ Mashima, K.⁶

48
- 85027923848
- Y. Kita, K. Yamaji, K. Higashida, K. Sathaiah, A. Iimuro, K. Mashima, Chem. Eur. J. 2015, 21, 1915-1927.
- (2015) Chem. Eur. J. , vol.21 , pp. 1915-1927
- Kita, Y.¹ Yamaji, K.² Higashida, K.³ Sathaiah, K.⁴ Iimuro, A.⁵ Mashima, K.⁶

49
- 84897725028
- Y. Kita, A. Iimuro, S. Hida, K. Mashima, Chem. Lett. 2014, 43, 284-286.
- (2014) Chem. Lett. , vol.43 , pp. 284-286
- Kita, Y.¹ Iimuro, A.² Hida, S.³ Mashima, K.⁴

50
- 84939269751
- M.-W. Chen, Z.-S. Ye, Z.-P. Chen, B. Wu, Y.-G. Zhou, Org. Chem. Front. 2015, 2, 586-589.
- (2015) Org. Chem. Front. , vol.2 , pp. 586-589
- Chen, M.-W.¹ Ye, Z.-S.² Chen, Z.-P.³ Wu, B.⁴ Zhou, Y.-G.⁵

51
- 84924021277
- Y. Kita, K. Higashida, K. Yamaji, A. Iimuro, K. Mashima, Chem. Commun. 2015, 51, 4380-4382.
- (2015) Chem. Commun. , vol.51 , pp. 4380-4382
- Kita, Y.¹ Higashida, K.² Yamaji, K.³ Iimuro, A.⁴ Mashima, K.⁵

52
- 85027926634
- Angew. Chem. 2015, 127, 2423
- R. Kuwano, Y. Hashiguchi, R. Ikeda, K. Ishizuka, Angew. Chem. Int. Ed. 2015, 54, 2393-2396; Angew. Chem. 2015, 127, 2423.
- (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 2393-2396
- Kuwano, R.¹ Hashiguchi, Y.² Ikeda, R.³ Ishizuka, K.⁴

53
- 58149202442
- Z.-W. Li, T.-L. Wang, Y.-M. He, Z.-J. Wang, Q.-H. Fan, J. Pan, L.-J. Xu, Org. Lett. 2008, 10, 5265-5268.
- (2008) Org. Lett. , vol.10 , pp. 5265-5268
- Li, Z.-W.¹ Wang, T.-L.² He, Y.-M.³ Wang, Z.-J.⁴ Fan, Q.-H.⁵ Pan, J.⁶ Xu, L.-J.⁷

54
- 84904999969
- X.-F. Cai, W.-X. Huang, Z.-P. Chen, Y.-G. Zhou, Chem. Commun. 2014, 50, 9588-9590.
- (2014) Chem. Commun. , vol.50 , pp. 9588-9590
- Cai, X.-F.¹ Huang, W.-X.² Chen, Z.-P.³ Zhou, Y.-G.⁴

55
- 53949112678
- N. Mršic, L. Lefort, J. A. F. Boogers, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Adv. Synth. Catal. 2008, 350, 1081-1089.
- (2008) Adv. Synth. Catal. , vol.350 , pp. 1081-1089
- Mršic, N.¹ Lefort, L.² Boogers, J.A.F.³ Minnaard, A.J.⁴ Feringa, B.L.⁵ De Vries, J.G.⁶

56
- 77951297663
- D.-S. Wang, Y.-G. Zhou, Tetrahedron Lett. 2010, 51, 3014-3017.
- (2010) Tetrahedron Lett. , vol.51 , pp. 3014-3017
- Wang, D.-S.¹ Zhou, Y.-G.²

57
- 67649132809
- Z.-J. Wang, H.-F. Zhou, T.-L. Wang, Y.-M. He, Q.-H. Fan, Green Chem. 2009, 11, 767-769.
- (2009) Green Chem. , vol.11 , pp. 767-769
- Wang, Z.-J.¹ Zhou, H.-F.² Wang, T.-L.³ He, Y.-M.⁴ Fan, Q.-H.⁵

58
- 78650673887
- J. L. Núñez-Rico, H. Fernández-Pérez, J. Benet-Buchholz, A. Vidal-Ferran, Organometallics 2010, 29, 6627-6631.
- (2010) Organometallics , vol.29 , pp. 6627-6631
- Núñez-Rico, J.L.¹ Fernández-Pérez, H.² Benet-Buchholz, J.³ Vidal-Ferran, A.⁴

59
- 70549106501
- N. Mršic, T. Jerphagnon, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Adv. Synth. Catal. 2009, 351, 2549-2552.
- (2009) Adv. Synth. Catal. , vol.351 , pp. 2549-2552
- Mršic, N.¹ Jerphagnon, T.² Minnaard, A.J.³ Feringa, B.L.⁴ De Vries, J.G.⁵

60
- 84876572872
- J. L. Núñez-Rico, A. Vidal-Ferran, Org. Lett. 2013, 15, 2066-2069.
- (2013) Org. Lett. , vol.15 , pp. 2066-2069
- Núñez-Rico, J.L.¹ Vidal-Ferran, A.²

61
- 84911442136
- Angew. Chem. 2014, 126, 12975
- M. Chang, Y. Huang, S. Liu, Y. Chen, S. W. Krska, I. W. Davies, X. Zhang, Angew. Chem. Int. Ed. 2014, 53, 12761-12764; Angew. Chem. 2014, 126, 12975.
- (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 12761-12764
- Chang, M.¹ Huang, Y.² Liu, S.³ Chen, Y.⁴ Krska, S.W.⁵ Davies, I.W.⁶ Zhang, X.⁷

62
- 84903141530
- W. X. Huang, C. B. Yu, L. Shi, Y. G. Zhou, Org. Lett. 2014, 16, 3324-3327.
- (2014) Org. Lett. , vol.16 , pp. 3324-3327
- Huang, W.X.¹ Yu, C.B.² Shi, L.³ Zhou, Y.G.⁴

63
- 21244463410
- C. Y. Legault, A. B. Charette, J. Am. Chem. Soc. 2005, 127, 8966-8967.
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 8966-8967
- Legault, C.Y.¹ Charette, A.B.²

64
- 61549122646
- C. Y. Legault, A. B. Charette, P. G. Cozzi, Heterocycles 2008, 76, 1271-1283.
- (2008) Heterocycles , vol.76 , pp. 1271-1283
- Legault, C.Y.¹ Charette, A.B.² Cozzi, P.G.³

65
- 33745576403
- Angew. Chem. 2006, 118, 2318
- S.-M. Lu, Y.-Q. Wang, X.-W. Han, Y.-G. Zhou, Angew. Chem. Int. Ed. 2006, 45, 2260-2263; Angew. Chem. 2006, 118, 2318.
- (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2260-2263
- Lu, S.-M.¹ Wang, Y.-Q.² Han, X.-W.³ Zhou, Y.-G.⁴

66
- 84867019830
- Angew. Chem. 2012, 124, 10328
- Z.-S. Ye, M.-W. Chen, Q.-A. Chen, L. Shi, Y. Duan, Y.-G. Zhou, Angew. Chem. Int. Ed. 2012, 51, 10181-10184; Angew. Chem. 2012, 124, 10328.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 10181-10184
- Ye, Z.-S.¹ Chen, M.-W.² Chen, Q.-A.³ Shi, L.⁴ Duan, Y.⁵ Zhou, Y.-G.⁶

67
- 84875322872
- Angew. Chem. 2013, 125, 3773
- Z.-S. Ye, R.-N. Guo, X.-F. Cai, M.-W. Chen, L. Shi, Y.-G. Zhou, Angew. Chem. Int. Ed. 2013, 52, 3685-3689; Angew. Chem. 2013, 125, 3773.
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 3685-3689
- Ye, Z.-S.¹ Guo, R.-N.² Cai, X.-F.³ Chen, M.-W.⁴ Shi, L.⁵ Zhou, Y.-G.⁶

68
- 84899845897
- A. Cadu, P. K. Upadhyay, P. G. Andersson, Asian J. Org. Chem. 2013, 2, 1061-1065.
- (2013) Asian J. Org. Chem. , vol.2 , pp. 1061-1065
- Cadu, A.¹ Upadhyay, P.K.² Andersson, P.G.³

69
- 84884411570
- A. M. Maj, I. Suisse, C. Hardouin, F. Agbossou-Niedercorn, Tetrahedron 2013, 69, 9322-9328.
- (2013) Tetrahedron , vol.69 , pp. 9322-9328
- Maj, A.M.¹ Suisse, I.² Hardouin, C.³ Agbossou-Niedercorn, F.⁴

70
- 0034625892
- R. Kuwano, K. Sato, T. Kurokawa, D. Karube, Y. Ito, J. Am. Chem. Soc. 2000, 122, 7614-7615.
- (2000) J. Am. Chem. Soc. , vol.122 , pp. 7614-7615
- Kuwano, R.¹ Sato, K.² Kurokawa, T.³ Karube, D.⁴ Ito, Y.⁵

71
- 3142732882
- R. Kuwano, K. Kaneda, T. Ito, K. Sato, T. Kurokawa, Y. Ito, Org. Lett. 2004, 6, 2213-2215.
- (2004) Org. Lett. , vol.6 , pp. 2213-2215
- Kuwano, R.¹ Kaneda, K.² Ito, T.³ Sato, K.⁴ Kurokawa, T.⁵ Ito, Y.⁶

72
- 33745579608
- R. Kuwano, M. Kashiwabara, Org. Lett. 2006, 8, 2653-2655.
- (2006) Org. Lett. , vol.8 , pp. 2653-2655
- Kuwano, R.¹ Kashiwabara, M.²

73
- 33645913553
- R. Kuwano, M. Kashiwabara, K. Sato, T. Ito, K. Kaneda, Y. Ito, Tetrahedron: Asymmetry 2006, 17, 521-535.
- (2006) Tetrahedron: Asymmetry , vol.17 , pp. 521-535
- Kuwano, R.¹ Kashiwabara, M.² Sato, K.³ Ito, T.⁴ Kaneda, K.⁵ Ito, Y.⁶

74
- 76449110295
- A. Baeza, A. Pfaltz, Chem. Eur. J. 2010, 16, 2036-2039.
- (2010) Chem. Eur. J. , vol.16 , pp. 2036-2039
- Baeza, A.¹ Pfaltz, A.²

75
- 76049091228
- N. Mršic, T. Jerphagnon, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Tetrahedron: Asymmetry 2010, 21, 7-10.
- (2010) Tetrahedron: Asymmetry , vol.21 , pp. 7-10
- Mršic, N.¹ Jerphagnon, T.² Minnaard, A.J.³ Feringa, B.L.⁴ De Vries, J.G.⁵

76
- 66449132887
- C.-B. Chen, X.-F. Wang, Y.-J. Cao, H.-G. Cheng, W.-J. Xiao, J. Org. Chem. 2009, 74, 3532-3535.
- (2009) J. Org. Chem. , vol.74 , pp. 3532-3535
- Chen, C.-B.¹ Wang, X.-F.² Cao, Y.-J.³ Cheng, H.-G.⁴ Xiao, W.-J.⁵

77
- 77954262931
- D.-S. Wang, Q.-A. Chen, W. Li, C.-B. Yu, Y.-G. Zhou, X. Zhang, J. Am. Chem. Soc. 2010, 132, 8909-8911.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 8909-8911
- Wang, D.-S.¹ Chen, Q.-A.² Li, W.³ Yu, C.-B.⁴ Zhou, Y.-G.⁵ Zhang, X.⁶

78
- 84901715796
- Y. Duan, L. Li, M.-W. Chen, C.-B. Yu, H.-J. Fan, Y.-G. Zhou, J. Am. Chem. Soc. 2014, 136, 7688-7700.
- (2014) J. Am. Chem. Soc. , vol.136 , pp. 7688-7700
- Duan, Y.¹ Li, L.² Chen, M.-W.³ Yu, C.-B.⁴ Fan, H.-J.⁵ Zhou, Y.-G.⁶

79
- 84859782761
- D.-Y. Zhang, C.-B. Yu, M.-C. Wang, K. Gao, Y.-G. Zhou, Tetrahedron Lett. 2012, 53, 2556-2559.
- (2012) Tetrahedron Lett. , vol.53 , pp. 2556-2559
- Zhang, D.-Y.¹ Yu, C.-B.² Wang, M.-C.³ Gao, K.⁴ Zhou, Y.-G.⁵

80
- 84879839869
- C. Li, J. Chen, G. Fu, D. Liu, Y. Liu, W. Zhang, Tetrahedron 2013, 69, 6839-6844.
- (2013) Tetrahedron , vol.69 , pp. 6839-6844
- Li, C.¹ Chen, J.² Fu, G.³ Liu, D.⁴ Liu, Y.⁵ Zhang, W.⁶

81
- 84894614166
- J. L. Núñez-Rico, H. Fernández-Pérez, A. Vidal-Ferran, Green Chem. 2014, 16, 1153-1157.
- (2014) Green Chem. , vol.16 , pp. 1153-1157
- Núñez-Rico, J.L.¹ Fernández-Pérez, H.² Vidal-Ferran, A.³

82
- 79958826410
- D.-S. Wang, Z.-S. Ye, Q.-A. Chen, Y.-G. Zhou, C.-B. Yu, H.-J. Fan, Y. Duan, J. Am. Chem. Soc. 2011, 133, 8866-8869.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 8866-8869
- Wang, D.-S.¹ Ye, Z.-S.² Chen, Q.-A.³ Zhou, Y.-G.⁴ Yu, C.-B.⁵ Fan, H.-J.⁶ Duan, Y.⁷

83
- 84929583132
- Z.-P. Chen, M.-W. Chen, L. Shi, C.-B. Yu, Y.-G. Zhou, Chem. Sci. 2015, 6, 3415-3419.
- (2015) Chem. Sci. , vol.6 , pp. 3415-3419
- Chen, Z.-P.¹ Chen, M.-W.² Shi, L.³ Yu, C.-B.⁴ Zhou, Y.-G.⁵

84
- 79955608899
- D.-S. Wang, J. Tang, Y.-G. Zhou, M.-W. Chen, C.-B. Yu, Y. Duan, G.-F. Jiang, Chem. Sci. 2011, 2, 803-806.
- (2011) Chem. Sci. , vol.2 , pp. 803-806
- Wang, D.-S.¹ Tang, J.² Zhou, Y.-G.³ Chen, M.-W.⁴ Yu, C.-B.⁵ Duan, Y.⁶ Jiang, G.-F.⁷

85
- 84939294482
- 3-(α-Hydroxyalkyl)indoles were synthesized by formylation of 2-substituted indoles followed by nucleophilic addition of Grignard reagents to the formyl group (see ref.^[48])
- 3-(α-Hydroxyalkyl)indoles were synthesized by formylation of 2-substituted indoles followed by nucleophilic addition of Grignard reagents to the formyl group (see ref.^[48]).

86
- 79958819430
- Y. Duan, M.-W. Chen, Z.-S. Ye, D.-S. Wang, Q.-A. Chen, Y.-G. Zhou, Chem. Eur. J. 2011, 17, 7193-7197.
- (2011) Chem. Eur. J. , vol.17 , pp. 7193-7197
- Duan, Y.¹ Chen, M.-W.² Ye, Z.-S.³ Wang, D.-S.⁴ Chen, Q.-A.⁵ Zhou, Y.-G.⁶

87
- 84862907714
- Y. Duan, M.-W. Chen, Q.-A. Chen, C.-B. Yu, Y.-G. Zhou, Org. Biomol. Chem. 2012, 10, 1235-1238.
- (2012) Org. Biomol. Chem. , vol.10 , pp. 1235-1238
- Duan, Y.¹ Chen, M.-W.² Chen, Q.-A.³ Yu, C.-B.⁴ Zhou, Y.-G.⁵

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