-
1
-
-
33644970374
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-
For some recent examples, see: a
-
For some recent examples, see: (a) Breslin, H. J.; Cai, C.; Miskowski, T. A.; Coutinho, S. V.; Zhang, S.-P.; Hornby, P.; He, W. Bioorg. Med. Chem. Lett. 2006, 16, 2505.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 2505
-
-
Breslin, H.J.1
Cai, C.2
Miskowski, T.A.3
Coutinho, S.V.4
Zhang, S.-P.5
Hornby, P.6
He, W.7
-
3
-
-
33748545633
-
-
(c) Balboni, G.; Onnis, V.; Congiu, C.; Zotti, M.; Sasaki, Y.; Ambo, A.; Bryant, S. D.; Jinsmaa, Y.; Lazarus, L. H.; Trapella, C.; Salvadori, S. J. Med. Chem. 2006, 49, 5610.
-
(2006)
J. Med. Chem
, vol.49
, pp. 5610
-
-
Balboni, G.1
Onnis, V.2
Congiu, C.3
Zotti, M.4
Sasaki, Y.5
Ambo, A.6
Bryant, S.D.7
Jinsmaa, Y.8
Lazarus, L.H.9
Trapella, C.10
Salvadori, S.11
-
4
-
-
0041624372
-
-
(a) Berger, R.; Rabbat, P. M. A.; Leighton, J. L. J. Am. Chem. Soc. 2003, 125, 9596.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 9596
-
-
Berger, R.1
Rabbat, P.M.A.2
Leighton, J.L.3
-
5
-
-
2442611756
-
-
(b) Berger, R.; Duff, K.; Leighton, J. L. J. Am. Chem. Soc. 2004, 126, 5686.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 5686
-
-
Berger, R.1
Duff, K.2
Leighton, J.L.3
-
6
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27944492745
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For a recent and comprehensive review of asymmetric imine allylation methods, see
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For a recent and comprehensive review of asymmetric imine allylation methods, see: Ding, H.; Friestad, G. K. Synthesis 2005, 2815.
-
(2005)
Synthesis
, pp. 2815
-
-
Ding, H.1
Friestad, G.K.2
-
7
-
-
33746256480
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-
We have recently shown in two different contexts that phenols are effective activators of our allylchlorosilane family of reagents: (a) Burns, N. Z, Hackman, B. M, Ng, P. Y, Powelson, I. A, Leighton, J. L. Angew. Chem, Int. Ed. 2006, 45, 3811
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We have recently shown in two different contexts that phenols are effective activators of our allylchlorosilane family of reagents: (a) Burns, N. Z.; Hackman, B. M.; Ng, P. Y.; Powelson, I. A.; Leighton, J. L. Angew. Chem., Int. Ed. 2006, 45, 3811.
-
-
-
-
8
-
-
33846167076
-
-
(b) Rabbat, P. M. A.; Valdez, S. C.; Leighton, J. L. Org. Lett. 2006, 8, 6119.
-
(2006)
Org. Lett
, vol.8
, pp. 6119
-
-
Rabbat, P.M.A.1
Valdez, S.C.2
Leighton, J.L.3
-
9
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34548544094
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As is the case with allylsilane 1, 4 is produced, isolated, and employed as a ∼2:1 mixture of diastereomers. See the Supporting Information
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As is the case with allylsilane 1, 4 is produced, isolated, and employed as a ∼2:1 mixture of diastereomers. See the Supporting Information.
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-
-
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10
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33751500827
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For other recent advances in asymmetric ketimine allylation, see: a
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For other recent advances in asymmetric ketimine allylation, see: (a) Hua, D. H.; Miao, S. W.; Chen, J. S.; Iguchi, S. J. Org. Chem. 1991, 56, 4.
-
(1991)
J. Org. Chem
, vol.56
, pp. 4
-
-
Hua, D.H.1
Miao, S.W.2
Chen, J.S.3
Iguchi, S.4
-
11
-
-
0033575410
-
-
(b) Cogan, D. A.; Liu, G.; Ellman, J. A. Tetrahedron 1999, 55, 8883.
-
(1999)
Tetrahedron
, vol.55
, pp. 8883
-
-
Cogan, D.A.1
Liu, G.2
Ellman, J.A.3
-
12
-
-
0036851670
-
-
(c) Ellman, J. A.; Owens, T. D.; Tang, T. P. Acc. Chem. Res. 2002, 35, 984.
-
(2002)
Acc. Chem. Res
, vol.35
, pp. 984
-
-
Ellman, J.A.1
Owens, T.D.2
Tang, T.P.3
-
13
-
-
33745033537
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-
(d) Wada, R.; Shibuguchi, T.; Makino, S.; Oisaki, K.; Kanai, M.; Shibasaki, M. J. Am. Chem. Soc. 2006, 128, 7687.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 7687
-
-
Wada, R.1
Shibuguchi, T.2
Makino, S.3
Oisaki, K.4
Kanai, M.5
Shibasaki, M.6
-
14
-
-
33745951212
-
-
(e) Canales, E.; Hernandez, E.; Soderquist, J. A. J. Am. Chem. Soc. 2006, 128, 8712.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 8712
-
-
Canales, E.1
Hernandez, E.2
Soderquist, J.A.3
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15
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0035829093
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Structurally related tertiary carbinamines have been accessed with, in some cases, very good diastereoselectivity employing the Ellman tert-butanesulfinimine methodology. See
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Structurally related tertiary carbinamines have been accessed with, in some cases, very good diastereoselectivity employing the Ellman tert-butanesulfinimine methodology. See: Shaw, A. W.; deSolms, S. J. Tetrahedron Lett. 2001, 42, 7173.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 7173
-
-
Shaw, A.W.1
deSolms, S.J.2
-
16
-
-
0033598258
-
-
(a) Scholl, M.; Ding, S.; Lee, C. W.; Grubbs, R. H. Org. Lett. 1999, 1, 953.
-
(1999)
Org. Lett
, vol.1
, pp. 953
-
-
Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
-
17
-
-
0034814443
-
-
(b) Sanford, M. S.; Love, J. A.; Grubbs, R. H. J. Am. Chem. Soc. 2001, 123, 6543.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 6543
-
-
Sanford, M.S.1
Love, J.A.2
Grubbs, R.H.3
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