SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Organic and Biomolecular Chemistry

Volumn 13, Issue 14, 2015, Pages 4260-4265

Visible light mediated sp3 C-H bond functionalization of N-aryl-1,2,3,4-tetrahydroisoquinolines via Ugi-type three-component reaction

(2) Chen, Yunyun a Feng, Gaofeng a

a SHAOXING UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACIDS; SYNTHESIS (CHEMICAL);

AEROBIC CONDITION; C-H BOND FUNCTIONALIZATION; HIGH-YIELD PROCESS; ISONITRILES; RU(BPY); THREE COMPONENT REACTIONS; VISIBLE LIGHT;

LIGHT;

EID: 84925703362 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c5ob00201j Document Type: Article

Times cited : (51)

References (52)

1
- 84894286870
- L. Ackermann Acc. Chem. Res. 2014 47 281 295
- (2014) Acc. Chem. Res. , vol.47 , pp. 281-295
- Ackermann, L.¹

2
- 84868355670
- P. Arockiam C. Bruneau P. Dixneuf Chem. Rev. 2012 112 5879 5918
- (2012) Chem. Rev. , vol.112 , pp. 5879-5918
- Arockiam, P.¹ Bruneau, C.² Dixneuf, P.³

3
- 84863451341
- S. Neufeldt M. Sanford Acc. Chem. Res. 2012 45 936 946
- (2012) Acc. Chem. Res. , vol.45 , pp. 936-946
- Neufeldt, S.¹ Sanford, M.²

4
- 80054105790
- J. Wencel-Delord T. Dröge F. Liu F. Glorius Chem. Soc. Rev. 2011 40 4740 4761
- (2011) Chem. Soc. Rev. , vol.40 , pp. 4740-4761
- Wencel-Delord, J.¹ Dröge, T.² Liu, F.³ Glorius, F.⁴

5
- 77349090183
- D. Colby R. Bergman J. Ellman Chem. Rev. 2010 110 624 655
- (2010) Chem. Rev. , vol.110 , pp. 624-655
- Colby, D.¹ Bergman, R.² Ellman, J.³

6
- 77349125577
- 3 C-H bonds adjacent to nitrogen, see
- I. Mkhalid J. Barnard T. Marder J. Murphy J. Hartwig Chem. Rev. 2010 110 890 931
- (2010) Chem. Rev. , vol.110 , pp. 890-931
- Mkhalid, I.¹ Barnard, J.² Marder, T.³ Murphy, J.⁴ Hartwig, J.⁵

7
- 84858079549
- K. Jones P. Karier M. Klussmann ChemCatChem 2012 4 51 54
- (2012) ChemCatChem , vol.4 , pp. 51-54
- Jones, K.¹ Karier, P.² Klussmann, M.³

8
- 79957764052
- E. Boess D. Sureshkumar A. Sud C. Wirtz C. Fares M. Klussmann J. Am. Chem. Soc. 2011 133 8106 8109
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 8106-8109
- Boess, E.¹ Sureshkumar, D.² Sud, A.³ Wirtz, C.⁴ Fares, C.⁵ Klussmann, M.⁶

9
- 79551702621
- J. Allen T. Lambert J. Am. Chem. Soc. 2011 133 1260 1262
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 1260-1262
- Allen, J.¹ Lambert, T.²

10
- 79751487205
- Y. Zhang H. Peng M. Zhang Y. Cheng C. Zhu Chem. Commun. 2011 47 2354 2356
- (2011) Chem. Commun. , vol.47 , pp. 2354-2356
- Zhang, Y.¹ Peng, H.² Zhang, M.³ Cheng, Y.⁴ Zhu, C.⁵

11
- 80054744489
- K. Alagiri G. Siddappa R. Kumara K. Prabhu Chem. Commun. 2011 47 11787 11789
- (2011) Chem. Commun. , vol.47 , pp. 11787-11789
- Alagiri, K.¹ Siddappa, G.² Kumara, R.³ Prabhu, K.⁴

12
- 50249118196
- S. Murahashi T. Nakae H. Terai N. Komiya J. Am. Chem. Soc. 2008 130 11005 11012
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 11005-11012
- Murahashi, S.¹ Nakae, T.² Terai, H.³ Komiya, N.⁴

13
- 18744386111
- Z. Li C. Li J. Am. Chem. Soc. 2005 127 6968 6969
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 6968-6969
- Li, Z.¹ Li, C.²

14
- 0346850026
- For selected examples, see
- S. Murahashi N. Komiya H. Terai T. Nakae J. Am. Chem. Soc. 2003 125 15312 15313
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 15312-15313
- Murahashi, S.¹ Komiya, N.² Terai, H.³ Nakae, T.⁴

15
- 33846905526
- A. Zhang J. Neumeyer R. Baldessarini Chem. Rev. 2007 107 274 302
- (2007) Chem. Rev. , vol.107 , pp. 274-302
- Zhang, A.¹ Neumeyer, J.² Baldessarini, R.³

16
- 33744954743
- K. Bentley Nat. Prod. Rep. 2006 23 444 463
- (2006) Nat. Prod. Rep. , vol.23 , pp. 444-463
- Bentley, K.¹

17
- 0036558479
- D. Jack R. Williams Chem. Rev. 2002 102 1669 1730
- (2002) Chem. Rev. , vol.102 , pp. 1669-1730
- Jack, D.¹ Williams, R.²

18
- 0037136379
- Q. Zhang G. Tu Y. Zhao T. Cheng Tetrahedron 2002 58 6795 6798
- (2002) Tetrahedron , vol.58 , pp. 6795-6798
- Zhang, Q.¹ Tu, G.² Zhao, Y.³ Cheng, T.⁴

19
- 0020600439
- A. Aladesanmi C. Kelly J. Leary J. Nat. Prod. 1983 46 127 131
- (1983) J. Nat. Prod. , vol.46 , pp. 127-131
- Aladesanmi, A.¹ Kelly, C.² Leary, J.³

20
- 84899845490
- A. Tanoue W. Yoo S. Kobayashi Org. Lett. 2014 16 2346 2349
- (2014) Org. Lett. , vol.16 , pp. 2346-2349
- Tanoue, A.¹ Yoo, W.² Kobayashi, S.³

21
- 84879508419
- M. Ratnikov X. Xu M. Doyle J. Am. Chem. Soc. 2013 135 9475 9479
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 9475-9479
- Ratnikov, M.¹ Xu, X.² Doyle, M.³

22
- 84874603381
- J. Dhineshkumar M. Lamani K. Alagiri K. Probhu Org. Lett. 2013 15 1092 1095
- (2013) Org. Lett. , vol.15 , pp. 1092-1095
- Dhineshkumar, J.¹ Lamani, M.² Alagiri, K.³ Probhu, K.⁴

23
- 84858633994
- E. Boess C. Schmitz M. Klussmann J. Am. Chem. Soc. 2012 134 5317 5325
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 5317-5325
- Boess, E.¹ Schmitz, C.² Klussmann, M.³

24
- 84875952448
- X. Liu B. Sun Z. Xie X. Qing L. Liu H. Lou J. Org. Chem. 2013 78 3104 3112
- (2013) J. Org. Chem. , vol.78 , pp. 3104-3112
- Liu, X.¹ Sun, B.² Xie, Z.³ Qing, X.⁴ Liu, L.⁵ Lou, H.⁶

25
- 84880521008
- For selected examples, see
- W. Muramatsu K. Nakano C. Li Org. Lett. 2013 15 3650 3653
- (2013) Org. Lett. , vol.15 , pp. 3650-3653
- Muramatsu, W.¹ Nakano, K.² Li, C.³

26
- 84898734503
- J. Zhong Q. Meng B. Liu X. Li X. Gao T. Lei C. Wu Z. Li C. Tung L. Wu Org. Lett. 2014 16 1988 1991
- (2014) Org. Lett. , vol.16 , pp. 1988-1991
- Zhong, J.¹ Meng, Q.² Liu, B.³ Li, X.⁴ Gao, X.⁵ Lei, T.⁶ Wu, C.⁷ Li, Z.⁸ Tung, C.⁹ Wu, L.¹⁰

27
- 84862755671
- W. Fu W. Guo G. Zou C. Xu J. Fluorine Chem. 2012 140 88 94
- (2012) J. Fluorine Chem. , vol.140 , pp. 88-94
- Fu, W.¹ Guo, W.² Zou, G.³ Xu, C.⁴

28
- 84870051028
- S. Zhu M. Rueping Chem. Commun. 2012 48 11960 11962
- (2012) Chem. Commun. , vol.48 , pp. 11960-11962
- Zhu, S.¹ Rueping, M.²

29
- 84859910319
- M. Rueping R. Koenigs K. Poscharny D. Fabry D. Leonori C. Vila Chem.-Eur. J. 2012 18 5170 5174
- (2012) Chem.-Eur. J. , vol.18 , pp. 5170-5174
- Rueping, M.¹ Koenigs, R.² Poscharny, K.³ Fabry, D.⁴ Leonori, D.⁵ Vila, C.⁶

30
- 84855476282
- D. Freeman L. Furst A. Condie C. Stephenson Org. Lett. 2012 14 94 97
- (2012) Org. Lett. , vol.14 , pp. 94-97
- Freeman, D.¹ Furst, L.² Condie, A.³ Stephenson, C.⁴

31
- 84863229256
- G. Zhao C. Yang L. Guo H. Sun C. Chen W. Xia Chem. Commun. 2012 48 2337 2339
- (2012) Chem. Commun. , vol.48 , pp. 2337-2339
- Zhao, G.¹ Yang, C.² Guo, L.³ Sun, H.⁴ Chen, C.⁵ Xia, W.⁶

32
- 81855173304
- M. Rueping S. Zhu R. M. Koenigs Chem. Commun. 2011 47 12709 12711
- (2011) Chem. Commun. , vol.47 , pp. 12709-12711
- Rueping, M.¹ Zhu, S.² Koenigs, R.M.³

33
- 79751515504
- M. Rueping C. Vila R. M. Koenigs K. Poscharny D. C. Fabry Chem. Commun. 2011 47 2360 2362
- (2011) Chem. Commun. , vol.47 , pp. 2360-2362
- Rueping, M.¹ Vila, C.² Koenigs, R.M.³ Poscharny, K.⁴ Fabry, D.C.⁵

34
- 79960504062
- M. Rueping S. Zhu R. M. Koenigs Chem. Commun. 2011 47 8679 8681
- (2011) Chem. Commun. , vol.47 , pp. 8679-8681
- Rueping, M.¹ Zhu, S.² Koenigs, R.M.³

35
- 82355191884
- Y. Pan S. Wang C. Kee E. Dubuisson Y. Yang K. Loh C. Tan Green Chem. 2011 13 3341 3344
- (2011) Green Chem. , vol.13 , pp. 3341-3344
- Pan, Y.¹ Wang, S.² Kee, C.³ Dubuisson, E.⁴ Yang, Y.⁵ Loh, K.⁶ Tan, C.⁷

36
- 84864469935
- G. Zhang Y. Ma S. Wang Y. Zhang R. Wang J. Am. Chem. Soc. 2012 134 12334 12337
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 12334-12337
- Zhang, G.¹ Ma, Y.² Wang, S.³ Zhang, Y.⁴ Wang, R.⁵

37
- 84859550640
- J. Zhang B. Tiwari C. Xing X. Chen R. Chi Angew. Chem., Int. Ed. 2012 51 3649 3652
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 3649-3652
- Zhang, J.¹ Tiwari, B.² Xing, C.³ Chen, X.⁴ Chi, R.⁵

38
- 84890935104
- W. Lin T. Cao W. Fan Y. Han J. Kuang H. Luo B. Miao X. Tang Q. Yu W. Yuan J. Zhang C. Zhu S. Ma Angew. Chem., Int. Ed. 2014 53 277 281
- (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 277-281
- Lin, W.¹ Cao, T.² Fan, W.³ Han, Y.⁴ Kuang, J.⁵ Luo, H.⁶ Miao, B.⁷ Tang, X.⁸ Yu, Q.⁹ Yuan, W.¹⁰ Zhang, J.¹¹ Zhu, C.¹² Ma, S.¹³

39
- 47749105369
- S. Murahashi D. Zhang Chem. Soc. Rev. 2008 37 1490 1501
- (2008) Chem. Soc. Rev. , vol.37 , pp. 1490-1501
- Murahashi, S.¹ Zhang, D.²

40
- 0026450952
- S. Murahashi T. Naota N. Miyaguchi T. Nakato Tetrahedron Lett. 1992 33 6991 6994
- (1992) Tetrahedron Lett. , vol.33 , pp. 6991-6994
- Murahashi, S.¹ Naota, T.² Miyaguchi, N.³ Nakato, T.⁴

41
- 33745157509
- Z. Li D. Bohle C. Li Proc. Natl. Acad. Sci. U. S. A. 2006 103 8928 8933
- (2006) Proc. Natl. Acad. Sci. U. S. A. , vol.103 , pp. 8928-8933
- Li, Z.¹ Bohle, D.² Li, C.³

42
- 4644355479
- Z. Li C. Li J. Am. Chem. Soc. 2004 126 11810 11811
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 11810-11811
- Li, Z.¹ Li, C.²

43
- 70349911749
- G. Jiang J. Chen J. Huang C. Che Org. Lett. 2009 11 4568 4571
- (2009) Org. Lett. , vol.11 , pp. 4568-4571
- Jiang, G.¹ Chen, J.² Huang, J.³ Che, C.⁴

44
- 34547403674
- T. Ngouansavanh J. Zhu Angew. Chem., Int. Ed. 2007 46 5775 5778
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 5775-5778
- Ngouansavanh, T.¹ Zhu, J.²

45
- 84880124916
- C. Prier D. Rankic D. MacMillan Chem. Rev. 2013 113 5322 5363
- (2013) Chem. Rev. , vol.113 , pp. 5322-5363
- Prier, C.¹ Rankic, D.² Macmillan, D.³

46
- 84868372230
- L. Shi W. Xia Chem. Soc. Rev. 2012 41 7687 7697
- (2012) Chem. Soc. Rev. , vol.41 , pp. 7687-7697
- Shi, L.¹ Xia, W.²

47
- 78650383080
- J. Marayanam C. Stephenson Chem. Soc. Rev. 2011 40 102 113
- (2011) Chem. Soc. Rev. , vol.40 , pp. 102-113
- Marayanam, J.¹ Stephenson, C.²

48
- 84906084928
- J. Tang J. Yue F. Tao G. Grampp B. Wang F. Li X. Liang Y. Shen J. Xu J. Org. Chem. 2014 79 7572 7582
- (2014) J. Org. Chem. , vol.79 , pp. 7572-7582
- Tang, J.¹ Yue, J.² Tao, F.³ Grampp, G.⁴ Wang, B.⁵ Li, F.⁶ Liang, X.⁷ Shen, Y.⁸ Xu, J.⁹

49
- 84877102165
- M. Rueping C. Vila Org. Lett. 2013 15 2092 2095
- (2013) Org. Lett. , vol.15 , pp. 2092-2095
- Rueping, M.¹ Vila, C.²

50
- 0037149057
- F. Kwong A. Klapars S. Buchwald Org. Lett. 2002 4 581 584
- (2002) Org. Lett. , vol.4 , pp. 581-584
- Kwong, F.¹ Klapars, A.² Buchwald, S.³

51
- 77956014076
- J. Kim D. Jang Synlett 2010 2093 2096
- (2010) Synlett , pp. 2093-2096
- Kim, J.¹ Jang, D.²

52
- 84925795788
- X. Wang Q. Wang Q. Luo Synthesis 2014 49 54
- (2014) Synthesis , pp. 49-54
- Wang, X.¹ Wang, Q.² Luo, Q.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.