-
1
-
-
33747663736
-
Recent review: H. Pellissier
-
Recent review: H. Pellissier, Tetrahedron 2006, 62, 5559-5601.
-
(2006)
Tetrahedron
, vol.62
, pp. 5559-5601
-
-
-
2
-
-
35948956235
-
-
a) F. Colobert, S. Choppin, L. Ferreiro-Mederos, M. Obringer, S. Luengo-Arratta, A. Urbano, M. C. Carreño, Org. Lett. 2007, 9, 4451-4454;
-
(2007)
Org. Lett
, vol.9
, pp. 4451-4454
-
-
Colobert, F.1
Choppin, S.2
Ferreiro-Mederos, L.3
Obringer, M.4
Luengo-Arratta, S.5
Urbano, A.6
Carreño, M.C.7
-
3
-
-
28844435328
-
-
b) M. C. Carreño, G. Hernández-Torres, A. Urbano, F. Colobert, Org. Lett. 2005, 7, 5517-5520;
-
(2005)
Org. Lett
, vol.7
, pp. 5517-5520
-
-
Carreño, M.C.1
Hernández-Torres, G.2
Urbano, A.3
Colobert, F.4
-
4
-
-
19544367629
-
-
c) M. C. Carreño, R. Des Mazery, A. Urbano, F. Colobert, G. Solladié, Org. Lett. 2005, 7, 2039-2042;
-
(2005)
Org. Lett
, vol.7
, pp. 2039-2042
-
-
Carreño, M.C.1
Des Mazery, R.2
Urbano, A.3
Colobert, F.4
Solladié, G.5
-
5
-
-
0842285209
-
-
d) M. C. Carreño, R. Des Mazery, A. Urbano, F. Colobert, G. Solladié, Org. Lett. 2004, 6, 297-299;
-
(2004)
Org. Lett
, vol.6
, pp. 297-299
-
-
Carreño, M.C.1
Des Mazery, R.2
Urbano, A.3
Colobert, F.4
Solladié, G.5
-
6
-
-
0141766891
-
-
e) M. C. Carreño, R. Des Mazery, A. Urbano, F. Colobert, G. Solladié, J. Org. Chem. 2003, 68, 7779-7787.
-
(2003)
J. Org. Chem
, vol.68
, pp. 7779-7787
-
-
Carreño, M.C.1
Des Mazery, R.2
Urbano, A.3
Colobert, F.4
Solladié, G.5
-
7
-
-
37649015786
-
-
Recent work: a E. T. Choi, M. H. Lee, Y. Kim, Y. S. Park, Tetrahedron 2008, 64, 1515-1522;
-
Recent work: a) E. T. Choi, M. H. Lee, Y. Kim, Y. S. Park, Tetrahedron 2008, 64, 1515-1522;
-
-
-
-
10
-
-
17444425377
-
-
d) C. Welter, A. Dahnz, B. Brunner, S. Streiff, P. Dübon, G. Helmchen, Org. Lett. 2005, 7, 1239-1242;
-
(2005)
Org. Lett
, vol.7
, pp. 1239-1242
-
-
Welter, C.1
Dahnz, A.2
Brunner, B.3
Streiff, S.4
Dübon, P.5
Helmchen, G.6
-
12
-
-
4644370085
-
-
f) B. M. Trost, H. C. Shen, L. Dong, J.-P. Surivet, C. Sylvain, J. Am. Chem. Soc. 2004, 126, 11966-11983;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 11966-11983
-
-
Trost, B.M.1
Shen, H.C.2
Dong, L.3
Surivet, J.-P.4
Sylvain, C.5
-
13
-
-
2942543484
-
-
g) M. Zhang, R. Reeves, Ch. Bi, R. Dally, G. Ladouceur, W. Bullock, J. Chin, Tetrahedron Lett. 2004, 45, 5229-5231;
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 5229-5231
-
-
Zhang, M.1
Reeves, R.2
Bi, C.3
Dally, R.4
Ladouceur, G.5
Bullock, W.6
Chin, J.7
-
15
-
-
0034635457
-
-
i) M. A. Birkett, D. W. Knight, P. B. Little, M. B. Mitchell, Tetrahedron 2000, 56, 1013-1023.
-
(2000)
Tetrahedron
, vol.56
, pp. 1013-1023
-
-
Birkett, M.A.1
Knight, D.W.2
Little, P.B.3
Mitchell, M.B.4
-
16
-
-
33746990729
-
-
Recent overview: a A. Veverka, D. S. Nuzum, J. L. Jolly, Ann. Pharmacother. 2006, 40, 1353-1360;
-
Recent overview: a) A. Veverka, D. S. Nuzum, J. L. Jolly, Ann. Pharmacother. 2006, 40, 1353-1360;
-
-
-
-
17
-
-
0025611395
-
-
early work: b G. Van Lommen, M. De Bruyn, M. Schroven, J. Pharm. Belg. 1990, 45, 355-360;
-
early work: b) G. Van Lommen, M. De Bruyn, M. Schroven, J. Pharm. Belg. 1990, 45, 355-360;
-
-
-
-
18
-
-
0024211087
-
-
c) P. J. Pauwells, W. Gommeren, G. Van Lommen, P. A. J. Janssen, J. E. Leysen, Mol. Pharm. 1988, 34, 843-851.
-
(1988)
Mol. Pharm
, vol.34
, pp. 843-851
-
-
Pauwells, P.J.1
Gommeren, W.2
Van Lommen, G.3
Janssen, P.A.J.4
Leysen, J.E.5
-
20
-
-
53749104851
-
-
The absolute configurations of (S,R)-5a and (S,S,S)-7 were established after X-ray diffraction. CCDC-673917 and CCDC-662529 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
-
The absolute configurations of (S,R)-5a and (S,S,S)-7 were established after X-ray diffraction. CCDC-673917 and CCDC-662529 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
-
-
-
-
21
-
-
53749088828
-
-
Recent work: a B. Parthasaradhi, K. Rathnakar, R. Raji, D. Muralidhara, I. Srinivas, WO 2007083318 A1, 2007;
-
Recent work: a) B. Parthasaradhi, K. Rathnakar, R. Raji, D. Muralidhara, I. Srinivas, WO 2007083318 A1, 2007;
-
-
-
-
22
-
-
53749100939
-
-
US 2007149612 A1, 2007;
-
b) T. Bader, A. Stutz, H. Hofmeier, H.-U. Bichsel, US 2007149612 A1, 2007;
-
-
-
Bader, T.1
Stutz, A.2
Hofmeier, H.3
Bichsel, H.-U.4
-
23
-
-
53749090959
-
-
WO 2007009143 A2, 2007;
-
c) Ch. R. Noe, M. Jasic, H. Kollmann, B. Lachmann, WO 2007009143 A2, 2007;
-
-
-
Noe, C.R.1
Jasic, M.2
Kollmann, H.3
Lachmann, B.4
-
25
-
-
53749105275
-
-
WO 2006025070 A2, 2006;
-
e) R. Sheth, S. V. Attanti, H. M. Patel, V. Gupta, S. S. Nadkarni, WO 2006025070 A2, 2006;
-
-
-
Sheth, R.1
Attanti, S.V.2
Patel, H.M.3
Gupta, V.4
Nadkarni, S.S.5
-
26
-
-
53749099982
-
-
WO 2006016376 A1, 2006;
-
f) R. B. Parthasaradhi, R. K. Rathnakar, R. R. Raji, R. D. Muralidhara, R. I. Srinivas, WO 2006016376 A1, 2006;
-
-
-
Parthasaradhi, R.B.1
Rathnakar, R.K.2
Raji, R.R.3
Muralidhara, R.D.4
Srinivas, R.I.5
-
27
-
-
33745022296
-
-
g) Y. X. Yang, N. X. Wang, Y. L. Xing, W. W. Wang, J. Zhao, G. X. Wang, S. Tang, Chin. Chem. Lett. 2005, 16, 1577-1580;
-
(2005)
Chin. Chem. Lett
, vol.16
, pp. 1577-1580
-
-
Yang, Y.X.1
Wang, N.X.2
Xing, Y.L.3
Wang, W.W.4
Zhao, J.5
Wang, G.X.6
Tang, S.7
-
28
-
-
53749086808
-
-
[4b] and h G. R. E. Van Lommen, M. F. L. De Bruyn, M. F. J. Schroven, EP 145067 A2, 1985.
-
[4b] and h) G. R. E. Van Lommen, M. F. L. De Bruyn, M. F. J. Schroven, EP 145067 A2, 1985.
-
-
-
-
29
-
-
34247629154
-
-
a) N.-X. Wang, A.-G. Yu, G.-X. Wang, X.-H. Zhang, Q.-S. Li, Z. Li, Synthesis 2007, 1154-1158;
-
(2007)
Synthesis
, pp. 1154-1158
-
-
Wang, N.-X.1
Yu, A.-G.2
Wang, G.-X.3
Zhang, X.-H.4
Li, Q.-S.5
Li, Z.6
-
30
-
-
53749104440
-
-
PCT Int. Appl, WO 2004041805 A1;
-
b) P. Trinka, J. Reiter, G. Berecz, G. Simig, PCT Int. Appl. 2004, WO 2004041805 A1;
-
(2004)
-
-
Trinka, P.1
Reiter, J.2
Berecz, G.3
Simig, G.4
-
32
-
-
0032569168
-
-
d) Ch. W. Johannes, M. S. Visser, G. S. Weatherhead, A. H. Hoveyda, J. Am. Chem. Soc. 1998, 120, 8340-8347;
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 8340-8347
-
-
Johannes, C.W.1
Visser, M.S.2
Weatherhead, G.S.3
Hoveyda, A.H.4
-
34
-
-
0037450179
-
-
M. C. Gutiérrez, V. Alphand, R. Furstoss, J. Mol. Catal. B 2003, 21, 231-238.
-
(2003)
J. Mol. Catal. B
, vol.21
, pp. 231-238
-
-
Gutiérrez, M.C.1
Alphand, V.2
Furstoss, R.3
-
35
-
-
53749105005
-
-
S. Akai, Y. Kita, Topics in Current Chemistry 274: Sulfur-Mediated Rearrangements I (Ed.: E. Schaumann), Springer, Berlin, 2007, pp. 35-76.
-
S. Akai, Y. Kita, Topics in Current Chemistry Vol. 274: Sulfur-Mediated Rearrangements I (Ed.: E. Schaumann), Springer, Berlin, 2007, pp. 35-76.
-
-
-
-
36
-
-
0008615308
-
-
Y. Arroyo-Gómez, J. F. Rodríguez-Amo, M. Santos-García, M. A. Sanz-Tejedor, Tetrahedron: Asymmetry 2000, 11, 789-796.
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 789-796
-
-
Arroyo-Gómez, Y.1
Rodríguez-Amo, J.F.2
Santos-García, M.3
Sanz-Tejedor, M.A.4
-
37
-
-
33947085552
-
-
The absolute configuration of diol (R,R)-12 was demonstrated after transformation into the corresponding Mosher's diesters: J. A. Dale, H. S. Mosher, J. Am. Chem. Soc. 1973, 95, 512-519.
-
The absolute configuration of diol (R,R)-12 was demonstrated after transformation into the corresponding Mosher's diesters: J. A. Dale, H. S. Mosher, J. Am. Chem. Soc. 1973, 95, 512-519.
-
-
-
-
38
-
-
53749103180
-
-
Nebivolol hydrochloride is marketed in Spain for the treatment of hypertension under the trade name Lobivon®
-
Nebivolol hydrochloride is marketed in Spain for the treatment of hypertension under the trade name Lobivon®.
-
-
-
-
39
-
-
53749098473
-
-
[8a]
-
[8a]
-
-
-
|