SCOPUS 정보 검색 플랫폼

Volumn 12, Issue 14, 2014, Pages 2189-2192

Direct sp3 C-H bond arylation, alkylation, and amidation of tetrahydroisoquinolines mediated by hypervalent iodine(iii) under mild conditions

(3) Muramatsu, Wataru a Nakano, Kimihiro a Li, Chao Jun b

a NAGASAKI UNIVERSITY (Japan)

b MCGILL UNIVERSITY (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDATION; ARYLATIONS; C-H BOND FUNCTIONALIZATION; GREEN SOLVENTS; HIGH YIELD; HYPERVALENT IODINE; QUATERNARY CARBON; TETRAHYDROISOQUINOLINES;

CHEMISTRY; POSITIVE IONS;

CHEMICAL COMPOUNDS;

AMIDE; IODINE; TETRAHYDROISOQUINOLINE DERIVATIVE;

ALKYLATION; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

ALKYLATION; AMIDES; IODINE; MOLECULAR STRUCTURE; TETRAHYDROISOQUINOLINES;

EID: 84903365505 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c3ob42354a Document Type: Article

Times cited : (46)

References (38)

1
- 65249146649
- C.-J. Li Acc. Chem. Res. 2009 42 335
- (2009) Acc. Chem. Res. , vol.42 , pp. 335
- Li, C.-J.¹

2
- 77957851120
- L. Liu P. E. Floreancig Org. Lett. 2010 12 4686
- (2010) Org. Lett. , vol.12 , pp. 4686
- Liu, L.¹ Floreancig, P.E.²

3
- 79951818730
- For examples, see
- A. S.-K. Tsang P. Jensen J. M. Hook A. S. K. Hashmi M. H. Todd Pure Appl. Chem. 2011 83 655
- (2011) Pure Appl. Chem. , vol.83 , pp. 655
- Tsang, A.S.-K.¹ Jensen, P.² Hook, J.M.³ Hashmi, A.S.K.⁴ Todd, M.H.⁵

4
- 0003593740
- ed., John Wiley & Sons, New York, Parts 1-3
- The Chemistry of Heterocyclic Compounds, ed., E. C. Taylor, A. Weissberger, John Wiley & Sons, New York, 1981, 1990, 1995, 38, Parts 1-3
- (1981) The Chemistry of Heterocyclic Compounds , vol.38
- Taylor, E.C.¹ Weissberger, A.²

5
- 0024951704
- P. S. Charifson Drugs Future 1989 14 1179
- (1989) Drugs Future , vol.14 , pp. 1179
- Charifson, P.S.¹

6
- 13044300880
- B. Hoffman S. J. Cho W. Zheng S. Wyrick D. E. Nichols R. B. Mailman A. Tropsha J. Med. Chem. 1999 42 3217
- (1999) J. Med. Chem. , vol.42 , pp. 3217
- Hoffman, B.¹ Cho, S.J.² Zheng, W.³ Wyrick, S.⁴ Nichols, D.E.⁵ Mailman, R.B.⁶ Tropsha, A.⁷

7
- 2642569156
- A. Ohtaka M. Ukai T. Hatanaka S. Kobayashi K. Ikeda S. Sato K. Miyata M. Sasamata Eur. J. Pharmacol. 2004 492 243
- (2004) Eur. J. Pharmacol. , vol.492 , pp. 243
- Ohtaka, A.¹ Ukai, M.² Hatanaka, T.³ Kobayashi, S.⁴ Ikeda, K.⁵ Sato, S.⁶ Miyata, K.⁷ Sasamata, M.⁸

8
- 5444230777
- L. Cardozo M. Lisec R. Millard O. V. Trip I. Kuzmin T. E. Drogendijk M. Huang A. M. Ridder J. Urol. 2004 172 1919
- (2004) J. Urol. , vol.172 , pp. 1919
- Cardozo, L.¹ Lisec, M.² Millard, R.³ Trip, O.V.⁴ Kuzmin, I.⁵ Drogendijk, T.E.⁶ Huang, M.⁷ Ridder, A.M.⁸

9
- 4143144122
- For examples, see
- R. A. Smulders W. J. Krauwinkel P. J. Swart M. Huang J. Clin. Pharmacol. 2004 44 1023
- (2004) J. Clin. Pharmacol. , vol.44 , pp. 1023
- Smulders, R.A.¹ Krauwinkel, W.J.² Swart, P.J.³ Huang, M.⁴

10
- 18744386111
- Z. Li C.-J. Li J. Am. Chem. Soc. 2005 127 6968
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 6968
- Li, Z.¹ Li, C.-J.²

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

12
- 84858633994
- E. Boess C. Schmitz M. Klussmann J. Am. Chem. Soc. 2012 134 5317
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 5317
- Boess, E.¹ Schmitz, C.² Klussmann, M.³

13
- 84855476282
- D. B. Freeman L. Faura A. G. Condie C. R. J. Stephenson Org. Lett. 2012 14 94
- (2012) Org. Lett. , vol.14 , pp. 94
- Freeman, D.B.¹ Faura, L.² Condie, A.G.³ Stephenson, C.R.J.⁴

14
- 84879508419
- M. O. Ratnikov X. Xu M. P. Doyle J. Am. Chem. Soc. 2013 135 9475
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 9475
- Ratnikov, M.O.¹ Xu, X.² Doyle, M.P.³

15
- 0026761162
- B. R. de Costa L. Radesca Synthesis 1992 887
- (1992) Synthesis , pp. 887
- De Costa, B.R.¹ Radesca, L.²

16
- 33747002718
- M. Ludwig C. E. Hoesl G. Höfner K. T. Wanner Eur. J. Med. Chem. 2006 41 1003
- (2006) Eur. J. Med. Chem. , vol.41 , pp. 1003
- Ludwig, M.¹ Hoesl, C.E.² Höfner, G.³ Wanner, K.T.⁴

17
- 33745157509
- Z. Li D. S. Bohle C.-J. Li Proc. Natl. Acad. Sci. U. S. A. 2006 103 8928
- (2006) Proc. Natl. Acad. Sci. U. S. A. , vol.103 , pp. 8928
- Li, Z.¹ Bohle, D.S.² Li, C.-J.³

18
- 56949091475
- O. Baslé C.-J. Li Org. Lett. 2008 10 3661
- (2008) Org. Lett. , vol.10 , pp. 3661
- Baslé, O.¹ Li, C.-J.²

19
- 78549232628
- M. Ghobrial K. Harhammer M. D. Mihovilovic M. Schnürch Chem. Commun. 2010 46 8836
- (2010) Chem. Commun. , vol.46 , pp. 8836
- Ghobrial, M.¹ Harhammer, K.² Mihovilovic, M.D.³ Schnürch, M.⁴

20
- 82255173962
- A. McNally C. K. Prier D. W. C. MacMillan Science 2011 334 1114
- (2011) Science , vol.334 , pp. 1114
- McNally, A.¹ Prier, C.K.² Macmillan, D.W.C.³

21
- 80055077308
- M. Ghobrial M. Schnürch M. D. Mihovilovic J. Org. Chem. 2011 76 8781
- (2011) J. Org. Chem. , vol.76 , pp. 8781
- Ghobrial, M.¹ Schnürch, M.² Mihovilovic, M.D.³

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

23
- 84872546191
- N. Dastbaravardeh K. Kirchner M. Schnürch M. D. Mihovilovic J. Org. Chem. 2013 78 658
- (2013) J. Org. Chem. , vol.78 , pp. 658
- Dastbaravardeh, N.¹ Kirchner, K.² Schnürch, M.³ Mihovilovic, M.D.⁴

24
- 84880521008
- -1, is reported on MSDS sheets For examples, see
- W. Muramatsu K. Nakano C.-J. Li Org. Lett. 2013 15 3650
- (2013) Org. Lett. , vol.15 , pp. 3650
- Muramatsu, W.¹ Nakano, K.² Li, C.-J.³

25
- 59049089106
- V. V. Zhdankin P. J. Stang Chem. Rev. 2008 108 5299
- (2008) Chem. Rev. , vol.108 , pp. 5299
- Zhdankin, V.V.¹ Stang, P.J.²

26
- 70449597257
- E. A. Merritt B. Olofsson Angew. Chem., Int. Ed. 2009 48 9052
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9052
- Merritt, E.A.¹ Olofsson, B.²

27
- 79952167902
- V. V. Zhdankin J. Org. Chem. 2011 76 1185
- (2011) J. Org. Chem. , vol.76 , pp. 1185
- Zhdankin, V.V.¹

28
- 79851503103
- A. Duschek S. F. Kirsch Angew. Chem., Int. Ed. 2011 50 1524
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 1524
- Duschek, A.¹ Kirsch, S.F.²

29
- 79651474136
- E. A. Merritt B. Olofsson Synthesis 2011 517
- (2011) Synthesis , pp. 517
- Merritt, E.A.¹ Olofsson, B.²

30
- 84855783504
- Y. Kita T. Dohi K. Morimoto J. Synth. Org. Chem. Jpn. 2011 69 1241
- (2011) J. Synth. Org. Chem. Jpn. , vol.69 , pp. 1241
- Kita, Y.¹ Dohi, T.² Morimoto, K.³

31
- 84862730541
- D. Fernandez Gonzalez F. Benfatti J. Waser ChemCatChem 2012 4 955
- (2012) ChemCatChem , vol.4 , pp. 955
- Fernandez Gonzalez, D.¹ Benfatti, F.² Waser, J.³

32
- 84858311791
- M. S. Yusubov V. V. Zhdankin Curr. Org. Synth. 2012 9 247
- (2012) Curr. Org. Synth. , vol.9 , pp. 247
- Yusubov, M.S.¹ Zhdankin, V.V.²

33
- 33847697029
- D. Aycock Org. Process Res. Dev. 2007 11 156
- (2007) Org. Process Res. Dev. , vol.11 , pp. 156
- Aycock, D.¹

34
- 0033613892
- D. Taniyama M. Hasegawa K. Tomioka Tetrahedron: Asymmetry 1999 10 221
- (1999) Tetrahedron: Asymmetry , vol.10 , pp. 221
- Taniyama, D.¹ Hasegawa, M.² Tomioka, K.³

35
- 33744941289
- M. D. Hossain T. Kitamura Bull. Chem. Soc. Jpn. 2006 79 142
- (2006) Bull. Chem. Soc. Jpn. , vol.79 , pp. 142
- Hossain, M.D.¹ Kitamura, T.²

36
- 33749509413
- T. K. Page T. Wirth Synthesis 2006 3153
- (2006) Synthesis , pp. 3153
- Page, T.K.¹ Wirth, T.²

37
- 77949812753
- 2O solution of PhMgBr with DDQ as an oxidant in PhCl gave 1 in 44% yield (the use of THF solution of PhMgBr gave in >99% yield) due to less solubility of DDQ or 2,3-dichloro-5,6-dicyanohydroquinone (DDHQ). See: ref. 5
- A. A. Zagulyaeva M. S. Yusubov V. V. Zhdankin J. Org. Chem. 2010 75 2119
- (2010) J. Org. Chem. , vol.75 , pp. 2119
- Zagulyaeva, A.A.¹ Yusubov, M.S.² Zhdankin, V.V.³

38
- 34247266658
- K. Watanabe N. Yamagiwa Y. Torisawa Org. Process Res. Dev. 2007 11 251
- (2007) Org. Process Res. Dev. , vol.11 , pp. 251
- Watanabe, K.¹ Yamagiwa, N.² Torisawa, Y.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.