-
2
-
-
54749090942
-
-
Angew. Chem. 2008, 120, 4716-4739;
-
(2008)
Angew. Chem.
, vol.120
, pp. 4716-4739
-
-
-
4
-
-
38349100690
-
-
S. Mukherjee, J. W. Yang, S. Hoffmann, B. List, 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
-
5
-
-
33947198541
-
-
D. Enders, C. Grondal, M. R. M. Hüttl, Angew. Chem. Int. Ed. 2007, 46, 1570-1581;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1570-1581
-
-
Enders, D.1
Grondal, C.2
Hüttl, M.R.M.3
-
6
-
-
34250678999
-
-
Angew. Chem. 2007, 119, 1590-1601;
-
(2007)
Angew. Chem.
, vol.119
, pp. 1590-1601
-
-
-
8
-
-
33746322013
-
-
Angew. Chem. 2006, 118, 1550-1573;
-
(2006)
Angew. Chem.
, vol.118
, pp. 1550-1573
-
-
-
10
-
-
84884712477
-
-
B. V. S. Reddy, M. Swain, S. M. Reddy, J. S. Yadav, RSC Adv. 2013, 3, 8756-8765;
-
(2013)
RSC Adv.
, vol.3
, pp. 8756-8765
-
-
Reddy, B.V.S.1
Swain, M.2
Reddy, S.M.3
Yadav, J.S.4
-
11
-
-
79954427396
-
-
R. Wu, X. Chang, A. Lu, Y. Wang, G. Wu, H. Song, Z. Zhou, C. Tang, Chem. Commun. 2011, 47, 5034-5036;
-
(2011)
Chem. Commun.
, vol.47
, pp. 5034-5036
-
-
Wu, R.1
Chang, X.2
Lu, A.3
Wang, Y.4
Wu, G.5
Song, H.6
Zhou, Z.7
Tang, C.8
-
12
-
-
82455167073
-
-
K. L. Kimmel, J. D. Weaver, J. A. Ellman, Chem. Sci. 2012, 3, 121-125;
-
(2012)
Chem. Sci.
, vol.3
, pp. 121-125
-
-
Kimmel, K.L.1
Weaver, J.D.2
Ellman, J.A.3
-
14
-
-
84861915312
-
-
K. L. Kimmel, J. D. Weaver, M. Lee, J. A. Ellman, J. Am. Chem. Soc. 2012, 134, 9058-9061.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 9058-9061
-
-
Kimmel, K.L.1
Weaver, J.D.2
Lee, M.3
Ellman, J.A.4
-
15
-
-
84883796483
-
-
J. A. Burkhard, G. Wuitschik, J.-M. Plancher, M. Rogers-Evans, E. M. Carreira, Org. Lett. 2013, 15, 4312-4315;
-
(2013)
Org. Lett.
, vol.15
, pp. 4312-4315
-
-
Burkhard, J.A.1
Wuitschik, G.2
Plancher, J.-M.3
Rogers-Evans, M.4
Carreira, E.M.5
-
16
-
-
79957479241
-
-
J. A. Burkhard, B. H. Tchitchanov, E. M. Carreira, Angew. Chem. Int. Ed. 2011, 50, 5379-5382;
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 5379-5382
-
-
Burkhard, J.A.1
Tchitchanov, B.H.2
Carreira, E.M.3
-
17
-
-
80052455299
-
-
Angew. Chem. 2011, 123, 5491-5494;
-
(2011)
Angew. Chem.
, vol.123
, pp. 5491-5494
-
-
-
18
-
-
79251489484
-
-
M. I. Vakulenko, L. V. Lapshina, S. I. Grishchenko, I. E. Efremova, V. M. Berestovitskaya, Russ. J. Gen. Chem. 2010, 80, 2393-2395;
-
(2010)
Russ. J. Gen. Chem.
, vol.80
, pp. 2393-2395
-
-
Vakulenko, M.I.1
Lapshina, L.V.2
Grishchenko, S.I.3
Efremova, I.E.4
Berestovitskaya, V.M.5
-
19
-
-
55949092663
-
-
J. C. Anderson, A. J. Blake, M. Mills, P. D. Ratcliffe, Org. Lett. 2008, 10, 4141-4143;
-
(2008)
Org. Lett.
, vol.10
, pp. 4141-4143
-
-
Anderson, J.C.1
Blake, A.J.2
Mills, M.3
Ratcliffe, P.D.4
-
20
-
-
0028928421
-
-
R. Schneider, P. Gerardin, B. Loubinoux, G. Rihs, Tetrahedron 1995, 51, 4997-5010;
-
(1995)
Tetrahedron
, vol.51
, pp. 4997-5010
-
-
Schneider, R.1
Gerardin, P.2
Loubinoux, B.3
Rihs, G.4
-
22
-
-
34247120129
-
-
For a review on asymmetric sulfa-Michael additions, see.
-
For a review on asymmetric sulfa-Michael additions, see:, D. Enders, Synthesis 2007, 959-980.
-
(2007)
Synthesis
, pp. 959-980
-
-
Enders, D.1
-
23
-
-
0036451588
-
-
For natural products containing the taurine motif, see
-
L. Della Corte, R. R. Crichton, G. Duburs, K. Nolan, K. F. Tipton, G. Tirzitis, R. J. Ward, Amino Acids 2002, 23, 367-379; For natural products containing the taurine motif, see:
-
(2002)
Amino Acids
, vol.23
, pp. 367-379
-
-
Della Corte, L.1
Crichton, R.R.2
Duburs, G.3
Nolan, K.4
Tipton, K.F.5
Tirzitis, G.6
Ward, R.J.7
-
24
-
-
64149100107
-
-
T. Ogata, T. Shimazaki, T. Umemoto, S. Kurata, T. Ohtsuki, T. Suzuki, T. Wada, J. Org. Chem. 2009, 74, 2585-2588;
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2585-2588
-
-
Ogata, T.1
Shimazaki, T.2
Umemoto, T.3
Kurata, S.4
Ohtsuki, T.5
Suzuki, T.6
Wada, T.7
-
25
-
-
0029114736
-
-
J. Kobayashi, S. Mikami, H. Shigemori, T. Takao, Y. Shimonishi, S. Izuta, S. Yoshida, Tetrahedron 1995, 51, 10487-10490;
-
(1995)
Tetrahedron
, vol.51
, pp. 10487-10490
-
-
Kobayashi, J.1
Mikami, S.2
Shigemori, H.3
Takao, T.4
Shimonishi, Y.5
Izuta, S.6
Yoshida, S.7
-
26
-
-
0029078819
-
-
H.-Y. Li, S. Matsunaga, N. Fusetani, J. Med. Chem. 1995, 38, 338-343;
-
(1995)
J. Med. Chem.
, vol.38
, pp. 338-343
-
-
Li, H.-Y.1
Matsunaga, S.2
Fusetani, N.3
-
28
-
-
0000642605
-
-
For drug molecules containing the taurine motif, see
-
H. Nakamura, H. Wu, J. Kobayashi, M. Kobayashi, Y. Ohizumi, Y. Hirata, J. Org. Chem. 1985, 50, 2494-2497; For drug molecules containing the taurine motif, see:
-
(1985)
J. Org. Chem.
, vol.50
, pp. 2494-2497
-
-
Nakamura, H.1
Wu, H.2
Kobayashi, J.3
Kobayashi, M.4
Ohizumi, Y.5
Hirata, Y.6
-
29
-
-
84969398817
-
-
S. Yang, M. Froeyen, E. Lescrinier, P. Marlière, P. Herdewijn, Org. Biomol. Chem. 2010, 8, 111-119;
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 111-119
-
-
Yang, S.1
Froeyen, M.2
Lescrinier, E.3
Marlière, P.4
Herdewijn, P.5
-
30
-
-
65349083270
-
-
C. Francavilla, E. Low, S. Nair, B. Kim, T. P. Shiau, D. Debabov, C. Celeri, N. Alvarez, A. Houchin, P. Xu, Bioorg. Med. Chem. Lett. 2009, 19, 2731-2734;
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2731-2734
-
-
Francavilla, C.1
Low, E.2
Nair, S.3
Kim, B.4
Shiau, T.P.5
Debabov, D.6
Celeri, C.7
Alvarez, N.8
Houchin, A.9
Xu, P.10
-
31
-
-
57749104804
-
-
E. Low, S. Nair, T. Shiau, B. Belisle, D. Debabov, C. Celeri, M. Zuck, R. Najafi, N. Georgopapadakou, R. Jain, Bioorg. Med. Chem. Lett. 2009, 19, 196-198.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 196-198
-
-
Low, E.1
Nair, S.2
Shiau, T.3
Belisle, B.4
Debabov, D.5
Celeri, C.6
Zuck, M.7
Najafi, R.8
Georgopapadakou, N.9
Jain, R.10
-
32
-
-
67649595327
-
-
K. L. Kimmel, M. T. Robak, J. A. Ellman, J. Am. Chem. Soc. 2009, 131, 8754-8755.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 8754-8755
-
-
Kimmel, K.L.1
Robak, M.T.2
Ellman, J.A.3
-
33
-
-
78649550137
-
-
J. A. Burkhard, G. Wuitschik, M. Rogers-Evans, K. Müller, E. M. Carreira, Angew. Chem. Int. Ed. 2010, 49, 9052-9067;
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 9052-9067
-
-
Burkhard, J.A.1
Wuitschik, G.2
Rogers-Evans, M.3
Müller, K.4
Carreira, E.M.5
-
34
-
-
79957496495
-
-
Angew. Chem. 2010, 122, 9236-9251;
-
(2010)
Angew. Chem.
, vol.122
, pp. 9236-9251
-
-
-
35
-
-
77951095524
-
-
G. Wuitschik, E. M. Carreira, B. Wagner, H. Fischer, I. Parrilla, F. Schuler, M. Rogers-Evans, K. Müller, J. Med. Chem. 2010, 53, 3227-3246.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3227-3246
-
-
Wuitschik, G.1
Carreira, E.M.2
Wagner, B.3
Fischer, H.4
Parrilla, I.5
Schuler, F.6
Rogers-Evans, M.7
Müller, K.8
-
36
-
-
0142072631
-
-
T. Okino, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2003, 125, 12672-12673;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 12672-12673
-
-
Okino, T.1
Hoashi, Y.2
Takemoto, Y.3
-
39
-
-
15444366940
-
-
B.-J. Li, L. Jiang, M. Liu, Y.-C. Chen, L.-S. Ding, Y. Wu, Synlett 2005, 603-606;
-
(2005)
Synlett
, pp. 603-606
-
-
Li, B.-J.1
Jiang, L.2
Liu, M.3
Chen, Y.-C.4
Ding, L.-S.5
Wu, Y.6
-
40
-
-
19544393388
-
-
B. Vakulya, S. Varga, A. Csampai, T. Soõs, Org. Lett. 2005, 7, 1967-1969;
-
(2005)
Org. Lett.
, vol.7
, pp. 1967-1969
-
-
Vakulya, B.1
Varga, S.2
Csampai, A.3
Soõs, T.4
-
42
-
-
32044439817
-
-
Angew. Chem. 2005, 117, 6525-6528;
-
(2005)
Angew. Chem.
, vol.117
, pp. 6525-6528
-
-
-
44
-
-
84957902029
-
-
Synthetic details, characterization, and molecular structures obtained by X-ray structural analysis of compounds are described in the Supporting Information. CCDC 1012329 (3 i) and 1012330 (3 j) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
-
Synthetic details, characterization, and molecular structures obtained by X-ray structural analysis of compounds are described in the Supporting Information. CCDC 1012329 (3 i) and 1012330 (3 j) 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.
-
-
-
-
45
-
-
84957902030
-
-
Precedent for the conversion of 1,2-nitrothioacetates to 1,2-aminosulfonic acids
-
Precedent for the conversion of 1,2-nitrothioacetates to 1,2-aminosulfonic acids:
-
-
-
|