-
1
-
-
33144477907
-
-
Meltzer, P. C.; Butler, D.; Deschamps, J. R.; Madras, B. K. J. Med. Chem. 2006, 49, 1420-1432
-
(2006)
J. Med. Chem.
, vol.49
, pp. 1420-1432
-
-
Meltzer, P.C.1
Butler, D.2
Deschamps, J.R.3
Madras, B.K.4
-
2
-
-
70449420106
-
-
Carrol, F. I.; Blough, B. E.; Abraham, P.; Mills, A. C.; Holleman, J. A.; Wolchenhauer, S. A.; Decker, A. M.; Landavazo, A. K.; McElroy, T.; Navarro, H. A.; Gatch, M. B.; Forster, M. J. J. Med. Chem. 2009, 52, 6768-6781
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6768-6781
-
-
Carrol, F.I.1
Blough, B.E.2
Abraham, P.3
Mills, A.C.4
Holleman, J.A.5
Wolchenhauer, S.A.6
Decker, A.M.7
Landavazo, A.K.8
McElroy, T.9
Navarro, H.A.10
Gatch, M.B.11
Forster, M.J.12
-
3
-
-
77149159458
-
-
Bouteiller, C.; Becerril-Ortega, J.; Marchand, P.; Nicole, O.; Barre, L.; Buisson, A.; Perrio, C. Org. Biomol. Chem. 2010, 8, 1111-1120
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 1111-1120
-
-
Bouteiller, C.1
Becerril-Ortega, J.2
Marchand, P.3
Nicole, O.4
Barre, L.5
Buisson, A.6
Perrio, C.7
-
4
-
-
18244400440
-
-
Meyers, M. C.; Wang, J.-L.; Iera, J. A.; Bang, J.-K.; Hara, T.; Saito, S.; Zambetti, G. P.; Appella, D. H. J. Am. Chem. Soc. 2005, 127, 6152-6153
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 6152-6153
-
-
Meyers, M.C.1
Wang, J.-L.2
Iera, J.A.3
Bang, J.-K.4
Hara, T.5
Saito, S.6
Zambetti, G.P.7
Appella, D.H.8
-
5
-
-
84887050019
-
-
EP 603769 A1 19940629
-
Ando, R.; Sakaki, T.; Morinaka, Y.; Takahashi, C.; Tamao, Y. EP 603769 A1 19940629, 1994.
-
(1994)
-
-
Ando, R.1
Sakaki, T.2
Morinaka, Y.3
Takahashi, C.4
Tamao, Y.5
-
8
-
-
84869384193
-
-
Matsuda, N.; Hirano, K.; Satoh, T.; Miura, M. Angew. Chem., Int. Ed. 2012, 51, 11827-11831
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 11827-11831
-
-
Matsuda, N.1
Hirano, K.2
Satoh, T.3
Miura, M.4
-
9
-
-
84867738173
-
-
Miura, T.; Morimoto, M.; Murakami, M. Org. Lett. 2012, 14, 5214-5217
-
(2012)
Org. Lett.
, vol.14
, pp. 5214-5217
-
-
Miura, T.1
Morimoto, M.2
Murakami, M.3
-
10
-
-
84865265565
-
-
Wei, Y.; Lin, S.; Liang, F. Org. Lett. 2012, 14, 4202-4205
-
(2012)
Org. Lett.
, vol.14
, pp. 4202-4205
-
-
Wei, Y.1
Lin, S.2
Liang, F.3
-
13
-
-
84865847452
-
-
Tian, J.-S.; Ng, K. W. J.; Wong, J.-R.; Loh, T.-P. Angew. Chem., Int. Ed. 2012, 51, 9105-9109
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 9105-9109
-
-
Tian, J.-S.1
Ng, K.W.J.2
Wong, J.-R.3
Loh, T.-P.4
-
14
-
-
33748621833
-
-
Guram, A. S.; Rennels, R. A.; Buchwald, S. L. Angew. Chem., Int. Ed. Engl. 1995, 34, 1348-1350
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 1348-1350
-
-
Guram, A.S.1
Rennels, R.A.2
Buchwald, S.L.3
-
16
-
-
0032492942
-
-
Chan, D. M. T.; Monaco, K. L.; Wang, R. P.; Winters, M. P. Tetrahedron Lett. 1998, 39, 2933
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2933
-
-
Chan, D.M.T.1
Monaco, K.L.2
Wang, R.P.3
Winters, M.P.4
-
17
-
-
0032493017
-
-
Lam, P.; Clark, C. G.; Saubern, S.; Adams, J.; Winters, M. P.; Chan, D. M.; Combs, T. A. Tetrahedron Lett. 1998, 39, 2941
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2941
-
-
Lam, P.1
Clark, C.G.2
Saubern, S.3
Adams, J.4
Winters, M.P.5
Chan, D.M.6
Combs, T.A.7
-
18
-
-
0038549003
-
-
Lam, P.; Vincent, G.; Bonne, D.; Clark, C. G. Tetrahedron Lett. 2003, 44, 4927
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 4927
-
-
Lam, P.1
Vincent, G.2
Bonne, D.3
Clark, C.G.4
-
19
-
-
80052330954
-
-
Harvey, J. S.; Simonovich, S. P.; Jamison, C. R.; MacMillan, D. W. C. J. Am. Chem. Soc. 2011, 133, 13782-13785
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13782-13785
-
-
Harvey, J.S.1
Simonovich, S.P.2
Jamison, C.R.3
Macmillan, D.W.C.4
-
23
-
-
82455205876
-
-
Simonovich, S. P.; Van Humbeck, J. F.; MacMillan, D. W. C. Chem. Sci. 2012, 3, 58-61
-
(2012)
Chem. Sci.
, vol.3
, pp. 58-61
-
-
Simonovich, S.P.1
Van Humbeck, J.F.2
Macmillan, D.W.C.3
-
28
-
-
84868141932
-
-
Kojima, Y.; Usui, K.; Kawaguchi, S. Bull. Chem. Soc. Jpn. 1972, 45, 3127-3130
-
(1972)
Bull. Chem. Soc. Jpn.
, vol.45
, pp. 3127-3130
-
-
Kojima, Y.1
Usui, K.2
Kawaguchi, S.3
-
31
-
-
0001447603
-
-
Alberti, A.; Canè, F.; Dembech, P.; Lazzari, D.; Ricci, A.; Seconi, G. J. Org. Chem. 1996, 61, 1677-1681
-
(1996)
J. Org. Chem.
, vol.61
, pp. 1677-1681
-
-
Alberti, A.1
Canè, F.2
Dembech, P.3
Lazzari, D.4
Ricci, A.5
Seconi, G.6
-
32
-
-
0030917964
-
-
Canè, F.; Brancaleoni, D.; Dembech, P.; Ricci, A.; Seconi, G. Synthesis 1997, 545-548
-
(1997)
Synthesis
, pp. 545-548
-
-
Canè, F.1
Brancaleoni, D.2
Dembech, P.3
Ricci, A.4
Seconi, G.5
-
33
-
-
33845303550
-
-
del Amo, C. L.; Dubbaka, S. R.; Krasovskiy, A.; Knochel, P. Angew. Chem., Int. Ed. 2006, 45, 7838-7842
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 7838-7842
-
-
Del Amo, C.L.1
Dubbaka, S.R.2
Krasovskiy, A.3
Knochel, P.4
-
34
-
-
34247643357
-
-
Kienle, M.; Dubbaka, S. R.; del Amo, V.; Knochel, P. Synthesis 2007, 1272-1278
-
(2007)
Synthesis
, pp. 1272-1278
-
-
Kienle, M.1
Dubbaka, S.R.2
Del Amo, V.3
Knochel, P.4
-
35
-
-
70350331575
-
-
Yang, L.; Lu, Z.; Stahl, S. S. Chem. Commun. 2009, 45, 6460-6462
-
(2009)
Chem. Commun.
, vol.45
, pp. 6460-6462
-
-
Yang, L.1
Lu, Z.2
Stahl, S.S.3
-
36
-
-
34347266926
-
-
Song, Y.-F.; van Albada, G. A.; Tang, J.; Mutikainen, I.; Turpeinen, U.; Massera, C.; Roubeau, O.; Costa, J. S.; Gamez, P.; Reedijk, J. Inorg. Chem. 2007, 46, 4944-4950
-
(2007)
Inorg. Chem.
, vol.46
, pp. 4944-4950
-
-
Song, Y.-F.1
Van Albada, G.A.2
Tang, J.3
Mutikainen, I.4
Turpeinen, U.5
Massera, C.6
Roubeau, O.7
Costa, J.S.8
Gamez, P.9
Reedijk, J.10
-
38
-
-
8444246718
-
-
Wei, H. X.; Jasoni, R. L.; Shao, H.; Hu, J.; Pare, P. W. Tetrahedron 2004, 60, 11829-11835
-
(2004)
Tetrahedron
, vol.60
, pp. 11829-11835
-
-
Wei, H.X.1
Jasoni, R.L.2
Shao, H.3
Hu, J.4
Pare, P.W.5
-
39
-
-
0000698247
-
-
2 see - 633
-
2; see: Kosower, E. M.; Cole, W. J.; Wu, G.-S.; Cardy, D. E.; Meisters, G. J. Org. Chem. 1963, 23, 630-633
-
(1963)
J. Org. Chem.
, vol.23
, pp. 630
-
-
Kosower, E.M.1
Cole, W.J.2
Wu, G.-S.3
Cardy, D.E.4
Meisters, G.5
-
40
-
-
0037241494
-
-
The substituted enolate derived from 2-butanone is substantially more π-nucleophilic, a feature that likely contributes to selective bromination and thereafter amination at the butanone 3-position. Mayr nucleophile index values for enol silanes are consistent with this finding - 77
-
The substituted enolate derived from 2-butanone is substantially more π-nucleophilic, a feature that likely contributes to selective bromination and thereafter amination at the butanone 3-position. Mayr nucleophile index values for enol silanes are consistent with this finding: Mayr, H.; Kempf, B.; Ofial, A. R. Acc. Chem. Res. 2003, 36, 66-77
-
(2003)
Acc. Chem. Res.
, vol.36
, pp. 66
-
-
Mayr, H.1
Kempf, B.2
Ofial, A.R.3
-
41
-
-
38349100690
-
-
Mukherjee, S.; Yang, J. W.; Hoffmann, S.; List, B. Chem. Rev. 2007, 107, 5471-5569
-
(2007)
Chem. Rev.
, vol.107
, pp. 5471-5569
-
-
Mukherjee, S.1
Yang, J.W.2
Hoffmann, S.3
List, B.4
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