-
1
-
-
34848848499
-
-
a) K. Müller, C. Faeh, F. Diederich, Science 2007, 317, 1881-1886;
-
(2007)
Science
, vol.317
, pp. 1881-1886
-
-
Müller, K.1
Faeh, C.2
Diederich, F.3
-
2
-
-
0003314351
-
Biomedical Frontiers of Fluorine Chemistry
-
Eds, I. Ojima, J. R. McCarthy, J. T. Welch, American Chemical Society, Washington, DC
-
b) Biomedical Frontiers of Fluorine Chemistry, ACS Symposium Series 639 (Eds.: I. Ojima, J. R. McCarthy, J. T. Welch), American Chemical Society, Washington, DC, 1996.
-
(1996)
ACS Symposium Series
, vol.639
-
-
-
3
-
-
53549095550
-
-
Recent reviews: a
-
Recent reviews: a) V. A. Brunet, D. O'Hagan, Angew. Chem. 2008, 120, 1198-1201;
-
(2008)
Angew. Chem
, vol.120
, pp. 1198-1201
-
-
Brunet, V.A.1
O'Hagan, D.2
-
4
-
-
41249087594
-
-
Angew. Chem. Int. Ed. 2008, 47, 1179-1182;
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 1179-1182
-
-
-
6
-
-
33747161381
-
-
c) P. M. Pihko, Angew. Chem. 2006, 118, 558-561;
-
(2006)
Angew. Chem
, vol.118
, pp. 558-561
-
-
Pihko, P.M.1
-
7
-
-
31044445377
-
-
Angew. Chem. Int. Ed. 2006, 45, 544-547;
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 544-547
-
-
-
9
-
-
33746318363
-
-
Angew. Chem. Int. Ed. 2006, 45, 2172-2174;
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 2172-2174
-
-
-
11
-
-
0001171313
-
-
K. Muñiz, Angew. Chem. 2001, 113, 1701-1704;
-
(2001)
Angew. Chem
, vol.113
, pp. 1701-1704
-
-
Muñiz, K.1
-
12
-
-
0038584547
-
-
and references 0therein
-
Angew. Chem. Int. Ed. 2001, 40, 1653-1656, and references 0therein.
-
(2001)
Angew. Chem. Int. Ed
, vol.40
, pp. 1653-1656
-
-
-
14
-
-
0034605873
-
-
Angew. Chem. Int. Ed. 2000, 39, 4359-4362;
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 4359-4362
-
-
-
15
-
-
0037065341
-
-
b) Y. Hamashima, K. Yagi, H. Takano, L. Tamas, M. Sodeoka, J. Am. Chem. Soc. 2002, 124, 14530-14531;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 14530-14531
-
-
Hamashima, Y.1
Yagi, K.2
Takano, H.3
Tamas, L.4
Sodeoka, M.5
-
17
-
-
27844604228
-
-
d) N. Shibata, J. Kohno, K. Takai, T. Ishimaru, S. Nakamura, T. Toru, S. Kanemasa, Angew. Chem. 2005, 117, 4276-4279;
-
(2005)
Angew. Chem
, vol.117
, pp. 4276-4279
-
-
Shibata, N.1
Kohno, J.2
Takai, K.3
Ishimaru, T.4
Nakamura, S.5
Toru, T.6
Kanemasa, S.7
-
18
-
-
22144453934
-
-
Angew. Chem. Int. Ed. 2005, 44, 4204-4207;
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 4204-4207
-
-
-
19
-
-
33947309578
-
-
e) K. Shibatomi, Y. Tsuzuki, S.-I. Nakata, Y. Sumikawa, S. Iwasa, Synlett 2007, 551-554.
-
(2007)
Synlett
, pp. 551-554
-
-
Shibatomi, K.1
Tsuzuki, Y.2
Nakata, S.-I.3
Sumikawa, Y.4
Iwasa, S.5
-
21
-
-
25144443583
-
-
b) M. Marigo, D. Fielenbach, A. Braunton, A. Kjoersgaard, K. A. Jørgensen, Angew. Chem. 2005, 117, 3769-3772;
-
(2005)
Angew. Chem
, vol.117
, pp. 3769-3772
-
-
Marigo, M.1
Fielenbach, D.2
Braunton, A.3
Kjoersgaard, A.4
Jørgensen, K.A.5
-
22
-
-
20444441594
-
-
Angew. Chem. Int. Ed. 2005, 44, 3703-3706;
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 3703-3706
-
-
-
24
-
-
25144445794
-
-
d) D. D. Steiner, N. Mase, C. F. Barbas III, Angew. Chem. 2005, 117, 3772-3776;
-
(2005)
Angew. Chem
, vol.117
, pp. 3772-3776
-
-
Steiner, D.D.1
Mase, N.2
Barbas III, C.F.3
-
25
-
-
20444494428
-
-
Angew. Chem. Int. Ed. 2005, 44, 3706-3710.
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 3706-3710
-
-
-
26
-
-
0141518173
-
-
Recently, Togni et al. reported the catalytic aymmetric synthesis of α,δ-chlorofluoro β-ketoesters with up to 65% ee. To the best of our knowledge, this is the only account of an enantioselective α,α-gem-halofluorination of carbonyl compound: R. Frantz, L. Hintermann, M. Perseghini, D. Broggini, A. Togni, Org. Lett. 2003, 5, 1709-1712.
-
Recently, Togni et al. reported the catalytic aymmetric synthesis of α,δ-chlorofluoro β-ketoesters with up to 65% ee. To the best of our knowledge, this is the only account of an enantioselective α,α-gem-halofluorination of carbonyl compound: R. Frantz, L. Hintermann, M. Perseghini, D. Broggini, A. Togni, Org. Lett. 2003, 5, 1709-1712.
-
-
-
-
27
-
-
0024801742
-
-
Diastereoselective syntheses or optical resolutions to give optically active α,α-halofluoro esters or amides and their transformations: a D. B. Bailey, A. N. Boa, G. A. Crofts, M. V. Diepen, M. Helliwell, R. E. Gammon, M. J. Harrison, Tetrahedron Lett. 1989, 30, 7457-7460;
-
Diastereoselective syntheses or optical resolutions to give optically active α,α-halofluoro esters or amides and their transformations: a) D. B. Bailey, A. N. Boa, G. A. Crofts, M. V. Diepen, M. Helliwell, R. E. Gammon, M. J. Harrison, Tetrahedron Lett. 1989, 30, 7457-7460;
-
-
-
-
28
-
-
0034826462
-
-
b) A. G. Myers, J. K. Barbay, B. Zhong, J. Am. Chem. Soc. 2001, 123, 7207-7219.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 7207-7219
-
-
Myers, A.G.1
Barbay, J.K.2
Zhong, B.3
-
29
-
-
1842863015
-
-
a) N. Halland, A. Braunton, S. Bachmann, M. Marigo, K. A. Jørgensen, J. Am. Chem. Soc. 2004, 126, 4790-4791;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4790-4791
-
-
Halland, N.1
Braunton, A.2
Bachmann, S.3
Marigo, M.4
Jørgensen, K.A.5
-
30
-
-
1842450587
-
-
b) M. P. Brochu, S. P. Brown, D. W. C. MacMillan, J. Am. Chem. Soc. 2004, 126, 4108-4109;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4108-4109
-
-
Brochu, M.P.1
Brown, S.P.2
MacMillan, D.W.C.3
-
31
-
-
0000921726
-
-
c) C. L. Stevens, E. Farkas, B. Gillis, J. Am. Chem. Soc. 1954, 76, 2695-2698.
-
(1954)
J. Am. Chem. Soc
, vol.76
, pp. 2695-2698
-
-
Stevens, C.L.1
Farkas, E.2
Gillis, B.3
-
32
-
-
9344239378
-
-
Y. Zhang, K. Shibatomi, H. Yamamoto, J. Am. Chem. Soc. 2004, 126, 15038-15039.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 15038-15039
-
-
Zhang, Y.1
Shibatomi, K.2
Yamamoto, H.3
-
33
-
-
53549132089
-
-
Organocatalytic asymmetric a chlorination of ketones: M. Marigo, S. Bachmann, H. Halland, A. Braunton, K. A. Jørgensen, Angew. Chem. 2004, 116, 5623-5626;
-
Organocatalytic asymmetric a chlorination of ketones: M. Marigo, S. Bachmann, H. Halland, A. Braunton, K. A. Jørgensen, Angew. Chem. 2004, 116, 5623-5626;
-
-
-
-
34
-
-
8444223916
-
-
Angew. Chem. Int. Ed. 2004, 43, 5507-5510.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 5507-5510
-
-
-
35
-
-
33846840892
-
-
Synthesis of fluorinated silyl enolates and their application to Pd-catalyzed asymmetric allylation reactions: É. Bélanger, K. Cantin, O. Messe, M. Tremblay, J.-F. Paquin, J. Am. Chem. Soc. 2007, 129, 1034-1035
-
Synthesis of fluorinated silyl enolates and their application to Pd-catalyzed asymmetric allylation reactions: É. Bélanger, K. Cantin, O. Messe, M. Tremblay, J.-F. Paquin, J. Am. Chem. Soc. 2007, 129, 1034-1035.
-
-
-
|