SCOPUS 정보 검색 플랫폼

Organic Chemistry Frontiers

Volumn 2, Issue 4, 2015, Pages 378-382

CO-enabled rhenium hydride catalyst for directed C(sp2)-H bond alkylation with olefins

(6) Jin, Hongming a Zhu, Zhengbo a Jin, Ning a Xie, Jin a Cheng, Yixiang a Zhu, Chengjian a,b

a NANJING UNIVERSITY (China)

b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; HYDRIDES; KETONES; OLEFINS;

ACTIVATED ALKENES; CARBONYL HYDRIDES; H-BONDS; HYDRIDE COMPLEXES; HYDROARYLATION; UNSATURATED KETONES;

RHENIUM COMPOUNDS;

EID: 84936851385 PISSN: 20524110 EISSN: 20524129 Source Type: Journal
DOI: 10.1039/c4qo00329b Document Type: Article

Times cited : (38)

References (44)

1
- 67649488045
- X. Chen K. M. Engle D. Wang J.-Q. Yu Angew. Chem., Int. Ed. 2009 48 5094
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 5094
- Chen, X.¹ Engle, K.M.² Wang, D.³ Yu, J.-Q.⁴

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

3
- 79952689970
- Y. Kuninobu K. Takai Chem. Rev. 2011 111 1938
- (2011) Chem. Rev. , vol.111 , pp. 1938
- Kuninobu, Y.¹ Takai, K.²

4
- 84868355670
- P. B. Arockiam C. Bruneau P. H. Dixneuf Chem. Rev. 2012 112 5879
- (2012) Chem. Rev. , vol.112 , pp. 5879
- Arockiam, P.B.¹ Bruneau, C.² Dixneuf, P.H.³

5
- 84874599469
- S. I. Kozhushkov L. Ackermann Chem. Sci. 2013 4 886
- (2013) Chem. Sci. , vol.4 , pp. 886
- Kozhushkov, S.I.¹ Ackermann, L.²

6
- 84894286870
- L. Ackermann Acc. Chem. Res. 2014 47 281
- (2014) Acc. Chem. Res. , vol.47 , pp. 281
- Ackermann, L.¹

7
- 84864153161
- L. Yang B. Qian H. Huang Chem.-Eur. J. 2012 18 9511
- (2012) Chem.-Eur. J. , vol.18 , pp. 9511
- Yang, L.¹ Qian, B.² Huang, H.³

8
- 84877257345
- Z. Shi C. Grohmann F. Glorius Angew. Chem., Int. Ed. 2013 52 5393
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 5393
- Shi, Z.¹ Grohmann, C.² Glorius, F.³

9
- 84877292512
- H. Wang N. Schröder F. Glorius Angew. Chem., Int. Ed. 2013 52 5386
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 5386
- Wang, H.¹ Schröder, N.² Glorius, F.³

10
- 84875698071
- M. Schinkel I. Marek L. Ackermann Angew. Chem., Int. Ed. 2013 52 3977
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 3977
- Schinkel, M.¹ Marek, I.² Ackermann, L.³

11
- 84876484708
- N. Hofmann L. Ackermann J. Am. Chem. Soc. 2013 135 5877
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 5877
- Hofmann, N.¹ Ackermann, L.²

12
- 79960274177
- K. Gao N. Yoshikai Angew. Chem., Int. Ed. 2011 50 6888
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6888
- Gao, K.¹ Yoshikai, N.²

13
- 84873907472
- T. Yoshino H. Ikemoto S. Matsunaga M. Kanai Angew. Chem., Int. Ed. 2013 52 2207
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2207
- Yoshino, T.¹ Ikemoto, H.² Matsunaga, S.³ Kanai, M.⁴

14
- 79251553730
- B. Li Z. Wu Y. Gu C. Sun B. Wang Z.-J. Shi Angew. Chem., Int. Ed. 2011 50 1109
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 1109
- Li, B.¹ Wu, Z.² Gu, Y.³ Sun, C.⁴ Wang, B.⁵ Shi, Z.-J.⁶

15
- 84878406179
- L. Jiao T. Bach Angew. Chem., Int. Ed. 2013 52 6080
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 6080
- Jiao, L.¹ Bach, T.²

16
- 53549084027
- G. Deng L. Zhao C. Li Angew. Chem., Int. Ed. 2008 47 6278
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 6278
- Deng, G.¹ Zhao, L.² Li, C.³

17
- 84894523383
- S. Yu X. Li Org. Lett. 2014 16 1200
- (2014) Org. Lett. , vol.16 , pp. 1200
- Yu, S.¹ Li, X.²

18
- 77952564249
- Z.-M. Sun J. Zhang R. S. Manan P. Zhao J. Am. Chem. Soc. 2010 132 6935
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 6935
- Sun, Z.-M.¹ Zhang, J.² Manan, R.S.³ Zhao, P.⁴

19
- 80053315014
- L. Yang C. A. Correia C. Li Org. Biomol. Chem. 2011 9 7176
- (2011) Org. Biomol. Chem. , vol.9 , pp. 7176
- Yang, L.¹ Correia, C.A.² Li, C.³

20
- 84908682221
- B. Zhou P. Ma H. Chen C. Wang Chem. Commun. 2014 50 14558
- (2014) Chem. Commun. , vol.50 , pp. 14558
- Zhou, B.¹ Ma, P.² Chen, H.³ Wang, C.⁴

21
- 33746110063
- Y. Kuninobu Y. Nishina M. Shouho K. Takai A. K. Takai Angew. Chem., Int. Ed. 2006 45 2766
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 2766
- Kuninobu, Y.¹ Nishina, Y.² Shouho, M.³ Takai, K.⁴ Takai, A.K.⁵

22
- 67651218689
- Y. Kuninobu T. Matsuk K. Takai J. Am. Chem. Soc. 2009 131 9914
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 9914
- Kuninobu, Y.¹ Matsuk, T.² Takai, K.³

23
- 30844466406
- Y. Kuninobu Y. Tokunaga A. Kawata K. Takai J. Am. Chem. Soc. 2006 128 202
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 202
- Kuninobu, Y.¹ Tokunaga, Y.² Kawata, A.³ Takai, K.⁴

24
- 84862909211
- D. Xia Y. Wang Z. Du Q. Zheng C. Wang Org. Lett. 2012 14 588
- (2012) Org. Lett. , vol.14 , pp. 588
- Xia, D.¹ Wang, Y.² Du, Z.³ Zheng, Q.⁴ Wang, C.⁵

25
- 84875716540
- Q. Tang D. Xia X. Jin Q. Zhang X. Sun C. Wang J. Am. Chem. Soc. 2013 135 4628
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 4628
- Tang, Q.¹ Xia, D.² Jin, X.³ Zhang, Q.⁴ Sun, X.⁵ Wang, C.⁶

26
- 84861594726
- Y. Fukumoto M. Daijo N. Chatani J. Am. Chem. Soc. 2012 134 8762
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 8762
- Fukumoto, Y.¹ Daijo, M.² Chatani, N.³

27
- 77957102792
- Y. Kuninobu P. Yu K. Takai Org. Lett. 2010 12 4274
- (2010) Org. Lett. , vol.12 , pp. 4274
- Kuninobu, Y.¹ Yu, P.² Takai, K.³

28
- 67149131858
- Y. Kuninobu Y. Fujii T. Matsuki Y. Nishina K. Takai Org. Lett. 2009 11 2711
- (2009) Org. Lett. , vol.11 , pp. 2711
- Kuninobu, Y.¹ Fujii, Y.² Matsuki, T.³ Nishina, Y.⁴ Takai, K.⁵

29
- 84886779743
- The syntheses of rhenium carbonyl compounds from perrhenate usually require dangerous elevated pressures (100-300 atm), high temperatures and long reaction times (up to 2 days)
- S. Sueki Y. Guo M. Kanai Y. Kuninobu Angew. Chem., Int. Ed. 2013 52 11879
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 11879
- Sueki, S.¹ Guo, Y.² Kanai, M.³ Kuninobu, Y.⁴

30
- 37049124472
- The price of potassium perrhenate is $3.3 per g
- J. Chatt R. S. Coffey J. Chem. Soc. A 1969 1963
- (1969) J. Chem. Soc. A , pp. 1963
- Chatt, J.¹ Coffey, R.S.²

31
- 0346344165
- G. A. Moehring C. C. Williams J. Buford M. Kaviani J. Sulko P. E. Fanwick Inorg. Chem. 1998 37 3848
- (1998) Inorg. Chem. , vol.37 , pp. 3848
- Moehring, G.A.¹ Williams, C.C.² Buford, J.³ Kaviani, M.⁴ Sulko, J.⁵ Fanwick, P.E.⁶

32
- 67349117788
- Y. Jimenez A. M. Strepka M. D. Borgohain P. A. Hinojosa G. A. Moehring Inorg. Chim. Acta 2009 362 3259
- (2009) Inorg. Chim. Acta , vol.362 , pp. 3259
- Jimenez, Y.¹ Strepka, A.M.² Borgohain, M.D.³ Hinojosa, P.A.⁴ Moehring, G.A.⁵

33
- 68249142761
- H. Takaya M. Ito H. Murahashi J. Am. Chem. Soc. 2009 131 10824
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 10824
- Takaya, H.¹ Ito, M.² Murahashi, H.³

34
- 84879735015
- P. P. M. Schleker R. Honeker J. Klankermayer W. Leitner ChemCatChem 2013 5 1762
- (2013) ChemCatChem , vol.5 , pp. 1762
- Schleker, P.P.M.¹ Honeker, R.² Klankermayer, J.³ Leitner, W.⁴

35
- 84885353613
- H. Jin J. Xie C. Pan Z. Zhu Y. Cheng C. Zhu ACS Catal. 2013 3 2195
- (2013) ACS Catal. , vol.3 , pp. 2195
- Jin, H.¹ Xie, J.² Pan, C.³ Zhu, Z.⁴ Cheng, Y.⁵ Zhu, C.⁶

36
- 77954271846
- F. Zhou Y. Liu J. Zhou Adv. Synth. Catal. 2010 352 1381
- (2010) Adv. Synth. Catal. , vol.352 , pp. 1381
- Zhou, F.¹ Liu, Y.² Zhou, J.³

37
- 84890940391
- C. Liu D. Liu W. Zhang L. Zhou A. Lei Org. Lett. 2013 15 6166
- (2013) Org. Lett. , vol.15 , pp. 6166
- Liu, C.¹ Liu, D.² Zhang, W.³ Zhou, L.⁴ Lei, A.⁵

38
- 79955669281
- K. Shen X. Liu G. Wang L. Lin X. Feng Angew. Chem., Int. Ed. 2011 50 4684
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 4684
- Shen, K.¹ Liu, X.² Wang, G.³ Lin, L.⁴ Feng, X.⁵

39
- 84913582685
- Less reductive hydrogen species derived from the decomposition of the rhenium hydride complex under standard conditions
- D. Sarraf N. Richy J. Vidal J. Org. Chem. 2014 79 10945
- (2014) J. Org. Chem. , vol.79 , pp. 10945
- Sarraf, D.¹ Richy, N.² Vidal, J.³

40
- 0001621191
- J. I. Levin S. M. Weinreb Tetrahedron Lett. 1982 23 2347
- (1982) Tetrahedron Lett. , vol.23 , pp. 2347
- Levin, J.I.¹ Weinreb, S.M.²

41
- 4644335808
- M. S. Babu K. M. L. Rai Tetrahedron Lett. 2004 45 7969
- (2004) Tetrahedron Lett. , vol.45 , pp. 7969
- Babu, M.S.¹ Rai, K.M.L.²

42
- 58149310556
- Y. Kuninobu Y. Nishina K. Okaguchi M. Shouho K. Takai Bull. Chem. Soc. Jpn. 2008 81 1393
- (2008) Bull. Chem. Soc. Jpn. , vol.81 , pp. 1393
- Kuninobu, Y.¹ Nishina, Y.² Okaguchi, K.³ Shouho, M.⁴ Takai, K.⁵

43
- 84891856961
- A large negative kinetic isotope effect is shown in the ESI Note that Kuninobu and Takai also investigated the KIE in the ortho-alkylation of 2-phenylpyridine with ethyl acrylate using rhenium carbonyl catalysis (see ref. 10a). In contrast to our system, they suggested that C-H oxidative addition was the rate determining step (KIE = 2.6)
- S. Ma G. Villa P. S. Thuy-Boun A. Homs J.-Q. Yu Angew. Chem., Int. Ed. 2014 53 734
- (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 734
- Ma, S.¹ Villa, G.² Thuy-Boun, P.S.³ Homs, A.⁴ Yu, J.-Q.⁵

44
- 30844452821
- M. Freni D. Giusto V. Valenti J. Inorg. Nucl. Chem. 1965 27 755
- (1965) J. Inorg. Nucl. Chem. , vol.27 , pp. 755
- Freni, M.¹ Giusto, D.² Valenti, V.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.