SCOPUS 정보 검색 플랫폼

Volumn , Issue 30, 2008, Pages 3552-3554

Convenient method for the rapid generation of highly active and enantioselective yttrium catalysts for asymmetric hydroamination

(5) Hannedouche, Jérôme a Aillaud, Isabelle a Collin, Jacqueline a Schulz, Emmanuelle a Trifonov, Alexander b

a UNIVERSITÉ PARIS SUD (France)

b G A RAZUVAEV INSTITUTE OF ORGANOMETALLIC CHEMISTRY (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; LITHIUM DERIVATIVE; YTTRIUM;

AMINATION; ARTICLE; CATALYST; CYCLIZATION; ENANTIOSELECTIVITY; PROTON NUCLEAR MAGNETIC RESONANCE; STOICHIOMETRY; SUBSTITUTION REACTION; SYNTHESIS;

EID: 47949118214 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b804745f Document Type: Article

Times cited : (53)

References (41)

1
- 35948944542
- I. Aillaud J. Collin J. Hannedouche E. Schulz Dalton Trans. 2007 5105
- (2007) Dalton Trans. , pp. 5105
- Aillaud, I.¹ Collin, J.² Hannedouche, J.³ Schulz, E.⁴

2
- 15044351895
- K. C. Hultzsch Adv. Synth. Catal. 2005 347 367
- (2005) Adv. Synth. Catal. , vol.347 , pp. 367
- Hultzsch, K.C.¹

3
- 4644336643
- S. Hong T. J. Marks Acc. Chem. Res. 2004 37 673
- (2004) Acc. Chem. Res. , vol.37 , pp. 673
- Hong, S.¹ Marks, T.J.²

4
- 0030838312
- R. Dorta P. Egli F. Zürcher A. Togni J. Am. Chem. Soc. 1997 110 10857
- (1997) J. Am. Chem. Soc. , vol.110 , pp. 10857
- Dorta, R.¹ Egli, P.² Zürcher, F.³ Togni, A.⁴

5
- 0034605453
- M. Kawatsura J. F. Hartwig J. Am. Chem. Soc. 2000 122 9546
- (2000) J. Am. Chem. Soc. , vol.122 , pp. 9546
- Kawatsura, M.¹ Hartwig, J.F.²

6
- 0034794048
- O. Löber M. Kawatsura J. F. Hartwig J. Am. Chem. Soc. 2001 123 4366
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 4366
- Löber, O.¹ Kawatsura, M.² Hartwig, J.F.³

7
- 0037415013
- K. Li P. N. Horton M. B. Hursthouse K. K. (M.) Hii J. Organomet. Chem. 2003 665 250
- (2003) J. Organomet. Chem. , vol.665 , pp. 250
- Li, K.¹ Horton, P.N.² Hursthouse, M.B.³ Hii, K.K.⁴

8
- 33750527134
- Other examples of chiral late transition metal-catalysed asymmetric hydroamination:
- A. Hu M. Ogasawara T. Sakamoto A. Okada K. Nakajima T. Takahashi W. Lin Adv. Synth. Catal. 2006 348 2051
- (2006) Adv. Synth. Catal. , vol.348 , pp. 2051
- Hu, A.¹ Ogasawara, M.² Sakamoto, T.³ Okada, A.⁴ Nakajima, K.⁵ Takahashi, T.⁶ Lin, W.⁷

9
- 1242291816
- L. M. Lutete I. Kadota Y. Yamamoto J. Am. Chem. Soc. 2004 126 1622
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 1622
- Lutete, L.M.¹ Kadota, I.² Yamamoto, Y.³

10
- 33847664670
- R. L. Lalonde B. D. Sherry E. J. Kang F. D. Toste J. Am. Chem. Soc. 2007 129 2452
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 2452
- Lalonde, R.L.¹ Sherry, B.D.² Kang, E.J.³ Toste, F.D.⁴

11
- 34547168414
- Z. Zhang C. F. Bender R. A. Widenhoefer Org. Lett. 2007 9 2887
- (2007) Org. Lett. , vol.9 , pp. 2887
- Zhang, Z.¹ Bender, C.F.² Widenhoefer, R.A.³

12
- 36448986032
- Z. Zhang C. F. Bender R. A. Widenhoefer J. Am. Chem. Soc. 2007 129 14148
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 14148
- Zhang, Z.¹ Bender, C.F.² Widenhoefer, R.A.³

13
- 1942500258
- P. D. Knight I. Munslow P. N. O'Shaughnessy P. Scott Chem. Commun. 2004 894
- (2004) Chem. Commun. , pp. 894
- Knight, P.D.¹ Munslow, I.² O'Shaughnessy, P.N.³ Scott, P.⁴

14
- 34047274289
- A. L. Gott A. J. Clarke G. J. Clarkson P. Scott Organometallics 2007 26 1729
- (2007) Organometallics , vol.26 , pp. 1729
- Gott, A.L.¹ Clarke, A.J.² Clarkson, G.J.³ Scott, P.⁴

15
- 33846422708
- M. C. Wood D. C. Leitch C. S. Yeung J. A. Kozak L. L. Schafer Angew. Chem., Int. Ed. 2007 46 354
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 354
- Wood, M.C.¹ Leitch, D.C.² Yeung, C.S.³ Kozak, J.A.⁴ Schafer, L.L.⁵

16
- 33749828529
- D. A. Watson M. Chiu R. G. Bergman Organometallics 2006 25 4731
- (2006) Organometallics , vol.25 , pp. 4731
- Watson, D.A.¹ Chiu, M.² Bergman, R.G.³

17
- 0001248656
- M. A. Giardello V. P. Conticello L. Brard M. Sabat A. L. Rheingold A. L. Stern T. J. Marks J. Am. Chem. Soc. 1994 116 10212
- (1994) J. Am. Chem. Soc. , vol.116 , pp. 10212
- Giardello, M.A.¹ Conticello, V.P.² Brard, L.³ Sabat, M.⁴ Rheingold, A.L.⁵ Stern, A.L.⁶ Marks, T.J.⁷

18
- 0000988919
- M. R. Douglass M. Ogasawara S. Hong M. V. Metz T. J. Marks Organometallics 2002 21 283
- (2002) Organometallics , vol.21 , pp. 283
- Douglass, M.R.¹ Ogasawara, M.² Hong, S.³ Metz, M.V.⁴ Marks, T.J.⁵

19
- 0345392827
- S. Hong S. Tian M. V. Metz T. J. Marks J. Am. Chem. Soc. 2003 125 14768
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 14768
- Hong, S.¹ Tian, S.² Metz, M.V.³ Marks, T.J.⁴

20
- 1242352508
- J.-S. Ryu T. J. Marks F. E. McDonald J. Org. Chem. 2004 69 1038
- (2004) J. Org. Chem. , vol.69 , pp. 1038
- Ryu, J.-S.¹ Marks, T.J.² McDonald, F.E.³

21
- 0037963641
- P. N. O'Shaughnessy P. D. Knight C. Morton K. M. Gillespie P. Scott Chem. Commun. 2003 1770
- (2003) Chem. Commun. , pp. 1770
- O'Shaughnessy, P.N.¹ Knight, P.D.² Morton, C.³ Gillespie, K.M.⁴ Scott, P.⁵

22
- 4344622278
- P. N. O'Shaughnessy K. M. Gillespie P. D. Knight I. J. Munslow P. Scott Dalton Trans. 2004 2251
- (2004) Dalton Trans. , pp. 2251
- O'Shaughnessy, P.N.¹ Gillespie, K.M.² Knight, P.D.³ Munslow, I.J.⁴ Scott, P.⁵

23
- 18844452146
- J. Y. Kim T. Livinghouse Org. Lett. 2005 7 1737
- (2005) Org. Lett. , vol.7 , pp. 1737
- Kim, J.Y.¹ Livinghouse, T.²

24
- 33845981091
- H. Kim Y. K. Kim J. H. Shim M. Kim M. Han T. Livinghouse P. H. Lee Adv. Synth. Catal. 2006 348 2609
- (2006) Adv. Synth. Catal. , vol.348 , pp. 2609
- Kim, H.¹ Kim, Y.K.² Shim, J.H.³ Kim, M.⁴ Han, M.⁵ Livinghouse, T.⁶ Lee, P.H.⁷

25
- 33748299170
- N. Meyer A. Zulys P. W. Roesky Organometallics 2006 25 4179
- (2006) Organometallics , vol.25 , pp. 4179
- Meyer, N.¹ Zulys, A.² Roesky, P.W.³

26
- 27144527276
- K. C. Hultzsch D. V. Gribkov F. Hampel J. Organomet. Chem. 2005 690 4441
- (2005) J. Organomet. Chem. , vol.690 , pp. 4441
- Hultzsch, K.C.¹ Gribkov, D.V.² Hampel, F.³

27
- 33645394124
- D. V. Gribkov K. C. Hultzsch F. Hampel J. Am. Chem. Soc. 2006 128 3748
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 3748
- Gribkov, D.V.¹ Hultzsch, K.C.² Hampel, F.³

28
- 0346880459
- J. Collin J.-C. Daran E. Schulz A. Trifonov Chem. Commun. 2003 3048
- (2003) Chem. Commun. , pp. 3048
- Collin, J.¹ Daran, J.-C.² Schulz, E.³ Trifonov, A.⁴

29
- 19944412195
- J. Collin J.-C. Daran O. Jacquet E. Schulz A. Trifonov Chem. Eur. J. 2005 11 3455
- (2005) Chem. Eur. J. , vol.11 , pp. 3455
- Collin, J.¹ Daran, J.-C.² Jacquet, O.³ Schulz, E.⁴ Trifonov, A.⁵

30
- 33645033199
- D. Riegert J. Collin A. Meddour E. Schulz A. Trifonov J. Org. Chem. 2006 71 2514
- (2006) J. Org. Chem. , vol.71 , pp. 2514
- Riegert, D.¹ Collin, J.² Meddour, A.³ Schulz, E.⁴ Trifonov, A.⁵

31
- 41749098446
- I. Aillaud J. Collin C. Duhayon R. Guillot D. Lyubov E. Schulz A. Trifonov Chem. Eur. J. 2008 14 2189
- (2008) Chem. Eur. J. , vol.14 , pp. 2189
- Aillaud, I.¹ Collin, J.² Duhayon, C.³ Guillot, R.⁴ Lyubov, D.⁵ Schulz, E.⁶ Trifonov, A.⁷

32
- 38349050030
- I. Aillaud K. Wright J. Collin E. Schulz J.-P. Mazaleyrat Tetrahedron: Asymmetry 2008 19 82
- (2008) Tetrahedron: Asymmetry , vol.19 , pp. 82
- Aillaud, I.¹ Wright, K.² Collin, J.³ Schulz, E.⁴ Mazaleyrat, J.-P.⁵

33
- 34250702600
- Lithium metal-based catalysts for asymmetric intramolecular hydroamination of alkenes were also reported:
- D. Riegert J. Collin J.-C. Daran T. Fillebeen E. Schulz D. Lyubov G. Fukin A. Trifonov Eur. J. Inorg. Chem. 2007 1159
- (2007) Eur. J. Inorg. Chem. , pp. 1159
- Riegert, D.¹ Collin, J.² Daran, J.-C.³ Fillebeen, T.⁴ Schulz, E.⁵ Lyubov, D.⁶ Fukin, G.⁷ Trifonov, A.⁸

34
- 33750341849
- P. Horrillo Martinez K. C. Hultzsch F. Hampel Chem. Commun. 2006 2221
- (2006) Chem. Commun. , pp. 2221
- Horrillo Martinez, P.¹ Hultzsch, K.C.² Hampel, F.³

35
- 34548011736
- A highly promising rhodium-catalysed intramolecular hydroamination of primary (and secondary) amines was recently reported:
- T. Ogata A. Ujihara S. Tsuchida T. Shimizu A. Kaneshige K. Tomioka Tetrahedron Lett. 2007 48 6648
- (2007) Tetrahedron Lett. , vol.48 , pp. 6648
- Ogata, T.¹ Ujihara, A.² Tsuchida, S.³ Shimizu, T.⁴ Kaneshige, A.⁵ Tomioka, K.⁶

36
- 38949090658
- For examples of in situ generated chiral catalysts using tris(organo or amido) rare-earth precursors for AIH: see refs. 5c,f,g,k This sequential metathetic route was also not suitable for the preparation of chiral diamido alkylyttrium complexes, see ref. 7
- Z. Liu J. F. Hartwig J. Am. Chem. Soc. 2008 130 1570
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 1570
- Liu, Z.¹ Hartwig, J.F.²

37
- 47949084397
- 3 was chosen for its tendency to afford stable neutral alkyl complexes. For examples of isolated chiral neutral bis(amido) alkyl yttrium bearing a methyl, ethyl or 1-hexyl group, see:
- Indeed, all lithium salts mentioned above were prepared by deprotonation of the related amine or diamine with n-BuLi in an individual reaction

38
- 0000187674
- For n-BuLi-catalysed intramolecular hydroamination of unactivated olefins:
- T. I. Gountchev T. D. Tilley Organometallics 1999 18 2896
- (1999) Organometallics , vol.18 , pp. 2896
- Gountchev, T.I.¹ Tilley, T.D.²

39
- 0037652138
- A. Ates C. Quinet Eur. J. Org. Chem. 2003 1623
- (2003) Eur. J. Org. Chem. , pp. 1623
- Ates, A.¹ Quinet, C.²

40
- 37449033063
- Review on rare-earth/alkali metal heterobimetallic complexes that catalyse various asymmetric reactions:
- C. Quinet P. Jourdain C. Hermans A. Ates I. Lucas I. E. Markó Tetrahedron 2008 64 1077
- (2008) Tetrahedron , vol.64 , pp. 1077
- Quinet, C.¹ Jourdain, P.² Hermans, C.³ Ates, A.⁴ Lucas, I.⁵ Markó, I.E.⁶

41
- 0036625219
- 3 and ligand in THF was chosen as the standard procedure For typical chemical shifts of methylene protons bound to yttrium, see ref. 14 No trace of yttrium amide ate complex bearing two chiral ligands per yttrium as previously described was observed in the spectrum6d For examples of the influence of THF or thiophene on the preparation of rare-earth metal catalysts for AIH, see, respectively refs. 5k and g
- M. Shibasaki N. Yoshikawa Chem. Rev. 2002 102 2187
- (2002) Chem. Rev. , vol.102 , pp. 2187
- Shibasaki, M.¹ Yoshikawa, N.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.