-
2
-
-
0033950079
-
-
B. K. Kay, M. P. Williamson, M. Sudol, FASEB J. 2000, 14, 231;
-
(2000)
FASEB J.
, vol.14
, pp. 231
-
-
Kay, B.K.1
Williamson, M.P.2
Sudol, M.3
-
5
-
-
4143114533
-
-
W. Notz, F. Tanaka, C. F. Barbas, III., Acc. Chem. Res. 2004, 37, 580;
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 580
-
-
Notz, W.1
Tanaka, F.2
Barbas III, C.F.3
-
6
-
-
38349178582
-
-
A. Erkkilä, I. Majander, P. M. Pihko, Chem. Rev. 2007, 107, 5416;
-
(2007)
Chem. Rev.
, vol.107
, pp. 5416
-
-
Erkkilä, A.1
Majander, I.2
Pihko, P.M.3
-
7
-
-
38349100690
-
-
S. Mukherjee, J. W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471;
-
(2007)
Chem. Rev.
, vol.107
, pp. 5471
-
-
Mukherjee, S.1
Yang, J.W.2
Hoffmann, S.3
List, B.4
-
8
-
-
43849098896
-
-
H. Kotsuki, H. Ikishima, A. Okuyama, Heterocycles 2008, 75, 493;
-
(2008)
Heterocycles
, vol.75
, pp. 493
-
-
Kotsuki, H.1
Ikishima, H.2
Okuyama, A.3
-
9
-
-
45249123858
-
-
H. Kotsuki, H. Ikishima, A. Okuyama, Heterocycles 2008, 75, 757;
-
(2008)
Heterocycles
, vol.75
, pp. 757
-
-
Kotsuki, H.1
Ikishima, H.2
Okuyama, A.3
-
13
-
-
26844568111
-
-
C. Nájera, J. M. Sansano, Angew. Chem. 2005, 117, 6428; Angew. Chem. Int. Ed. 2005, 44, 6272;
-
(2005)
Angew. Chem. 2005, 117, 6428; Angew. Chem. Int. Ed.
, vol.44
, pp. 6272
-
-
Nájera, C.1
Sansano, J.M.2
-
14
-
-
38149046540
-
-
A. Trabocchi, D. Scarpi, A. Guarna, Amino Acids 2008, 34, 1;
-
(2008)
Amino Acids
, vol.34
, pp. 1
-
-
Trabocchi, A.1
Scarpi, D.2
Guarna, A.3
-
18
-
-
79960576767
-
-
E. Busto, V. Gotor-Fernández, V. Gotor, Chem. Rev. 2011, 111, 3998.
-
(2011)
Chem. Rev.
, vol.111
, pp. 3998
-
-
Busto, E.1
Gotor-Fernández, V.2
Gotor, V.3
-
19
-
-
0029997094
-
-
P. P. Waid, G. A. Flynn, E. W. Huber, J. S. Sabol, Tetrahedron Lett. 1996, 37, 4091;
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4091
-
-
Waid, P.P.1
Flynn, G.A.2
Huber, E.W.3
Sabol, J.S.4
-
20
-
-
0035803034
-
-
T. M. Kamenecka, Y.-J. Park, L. S. Lin, T., Jr. Lanza, W. K. Hagmann, Tetrahedron Lett. 2001, 42, 8571;
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8571
-
-
Kamenecka, T.M.1
Park, Y.-J.2
Lin, L.S.3
Lanza, T.J.4
Hagmann, W.K.5
-
22
-
-
0037459690
-
-
P. Karoyan, J. Quancard, J. Vaissermann, G. Chassaing, J. Org. Chem. 2003, 68, 2256;
-
(2003)
J. Org. Chem.
, vol.68
, pp. 2256
-
-
Karoyan, P.1
Quancard, J.2
Vaissermann, J.3
Chassaing, G.4
-
23
-
-
8644274669
-
-
J. Quancard, A. Labonne, Y. Jacquot, G. Chassaing, S. Lavielle, P. Karoyan, J. Org. Chem. 2004, 69, 7940;
-
(2004)
J. Org. Chem.
, vol.69
, pp. 7940
-
-
Quancard, J.1
Labonne, A.2
Jacquot, Y.3
Chassaing, G.4
Lavielle, S.5
Karoyan, P.6
-
24
-
-
35748967901
-
-
R. Rios, I. Ibrahem, J. Vesely, H. Sundén, A. Córdova, Tetrahedron Lett. 2007, 48, 8695;
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8695
-
-
Rios, R.1
Ibrahem, I.2
Vesely, J.3
Sundén, H.4
Córdova, A.5
-
25
-
-
51549105915
-
-
C. Mothes, S. Lavielle, P. Karoyan, J. Org. Chem. 2008, 73, 6706;
-
(2008)
J. Org. Chem.
, vol.73
, pp. 6706
-
-
Mothes, C.1
Lavielle, S.2
Karoyan, P.3
-
26
-
-
56949087464
-
-
M. Oba, T. Saegusa, N. Nishiyama, K. Nishiyama, Tetrahedron 2009, 65, 128;
-
(2009)
Tetrahedron
, vol.65
, pp. 128
-
-
Oba, M.1
Saegusa, T.2
Nishiyama, N.3
Nishiyama, K.4
-
27
-
-
77955100690
-
-
P.-O. Delaye, J.-L. Vasse, J. Szymonisak, Org. Biomol. Chem. 2010, 8, 3635;
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 3635
-
-
Delaye, P.-O.1
Vasse, J.-L.2
Szymonisak, J.3
-
28
-
-
78651484734
-
-
P. Huy, J.-M. Neudörfl, H.-G. Schmalz, Org. Lett. 2011, 13, 216.
-
(2011)
Org. Lett.
, vol.13
, pp. 216
-
-
Huy, P.1
Neudörfl, J.-M.2
Schmalz, H.-G.3
-
29
-
-
0035908153
-
-
E. M. Stocking, J. F. Sanz-Cervera, C. J. Unkefer, R. M. Williams, Tetrahedron 2001, 57, 5303;
-
(2001)
Tetrahedron
, vol.57
, pp. 5303
-
-
Stocking, E.M.1
Sanz-Cervera, J.F.2
Unkefer, C.J.3
Williams, R.M.4
-
30
-
-
0034830338
-
-
E. M. Stocking, R. A. Martinez, L. A. Silks, J. F. Sanz-Cervera, R. M. Williams, J. Am. Chem. Soc. 2001, 123, 3391;
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 3391
-
-
Stocking, E.M.1
Martinez, R.A.2
Silks, L.A.3
Sanz-Cervera, J.F.4
Williams, R.M.5
-
31
-
-
0242460571
-
-
L. T. Tan, X. C. Cheng, P. R. Jensen, W. Fenical, J. Org. Chem. 2003, 68, 8767.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 8767
-
-
Tan, L.T.1
Cheng, X.C.2
Jensen, P.R.3
Fenical, W.4
-
32
-
-
9844223916
-
-
D. Y. Jackson, C. Quan, D. R. Artis, T. Rawson, B. Blackburn, M. Struble, G. Fitzgerald, K. Chan, S. Mullins, J. P. Burnier, W. J. Fairbrother, K. Clark, M. Berisini, H. Chui, M. Renz, S. Jones, S. Fong, J. Med. Chem. 1997, 40, 3359;
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3359
-
-
Jackson, D.Y.1
Quan, C.2
Artis, D.R.3
Rawson, T.4
Blackburn, B.5
Struble, M.6
Fitzgerald, G.7
Chan, K.8
Mullins, S.9
Burnier, J.P.10
Fairbrother, W.J.11
Clark, K.12
Berisini, M.13
Chui, H.14
Renz, M.15
Jones, S.16
Fong, S.17
-
33
-
-
0033618477
-
-
F. Micheli, R. D. Fabio, C. Marchioro, Farmaco 1999, 54, 461;
-
(1999)
Farmaco
, vol.54
, pp. 461
-
-
Micheli, F.1
Fabio, R.D.2
Marchioro, C.3
-
34
-
-
0033615593
-
-
Z. S. Zhou, A. Flohr, D. Hilvert, J. Org. Chem. 1999, 64, 8334;
-
(1999)
J. Org. Chem.
, vol.64
, pp. 8334
-
-
Zhou, Z.S.1
Flohr, A.2
Hilvert, D.3
-
35
-
-
0033551723
-
-
D. Damour, F. Herman, R. Labaudinière, G. Pantel, M. Vuilhorgne, S. Mignani, Tetrahedron 1999, 55, 10135;
-
(1999)
Tetrahedron
, vol.55
, pp. 10135
-
-
Damour, D.1
Herman, F.2
Labaudinière, R.3
Pantel, G.4
Vuilhorgne, M.5
Mignani, S.6
-
36
-
-
0346363687
-
-
J. Quancard, P. Karoyan, O. Lequin, E. Wenger, A. Aubry, S. Lavielle, G. Chassaing, Tetrahedron Lett. 2004, 45, 623;
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 623
-
-
Quancard, J.1
Karoyan, P.2
Lequin, O.3
Wenger, E.4
Aubry, A.5
Lavielle, S.6
Chassaing, G.7
-
37
-
-
33846032289
-
-
Y. Jacquot, I. Broutin, E. Miclet, M. Nicaise, O. Lequin, N. Goasdoué, C. Joss, P. Karoyan, M. Desmadril, A. Ducruix, S. Lavielle, Bioorg. Med. Chem. 2007, 15, 1439;
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 1439
-
-
Jacquot, Y.1
Broutin, I.2
Miclet, E.3
Nicaise, M.4
Lequin, O.5
Goasdoué, N.6
Joss, C.7
Karoyan, P.8
Desmadril, M.9
Ducruix, A.10
Lavielle, S.11
-
38
-
-
66149116389
-
-
C. Armishaw, A. A. Jensen, T. Balle, R. J. Clark, K. Harpsøe, C. Skonberg, T. Liljefors, K. Strømgaard, J. Biol. Chem. 2009, 284, 9498;
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 9498
-
-
Armishaw, C.1
Jensen, A.A.2
Balle, T.3
Clark, R.J.4
Harpsøe, K.5
Skonberg, C.6
Liljefors, T.7
Strømgaard, K.8
-
39
-
-
79951847471
-
-
A. M. Larsen, R. Venskutonyte, E. A. Valadés, B. Nielsen, D. S. Pickering, L. Bunch, ACS Chem. Neurosci. 2011, 2, 107.
-
(2011)
ACS Chem. Neurosci.
, vol.2
, pp. 107
-
-
Larsen, A.M.1
Venskutonyte, R.2
Valadés, E.A.3
Nielsen, B.4
Pickering, D.S.5
Bunch, L.6
-
40
-
-
84899804562
-
-
For recent reviews on asymmetric phase-transfer catalysis
-
For recent reviews on asymmetric phase-transfer catalysis, see:
-
-
-
-
46
-
-
34447272888
-
-
T. Ooi, K. Maruoka, Angew. Chem. 2007, 119, 4300; Angew. Chem. Int. Ed. 2007, 46, 4222;
-
(2007)
Angew. Chem. 2007, 119, 4300; Angew. Chem. Int. Ed.
, vol.46
, pp. 4222
-
-
Ooi, T.1
Maruoka, K.2
-
52
-
-
84899791469
-
-
Asymmetric synthesis of cyclic amino acids based on the phase-transfer-catalyzed conjugate additions
-
Asymmetric synthesis of cyclic amino acids based on the phase-transfer-catalyzed conjugate additions, see:
-
-
-
-
53
-
-
33746277828
-
-
T. Shibuguchi, H. Mihara, A. Kuramochi, S. Sakuraba, T. Ohshima, M. Shibasaki, Angew. Chem. 2006, 118, 4751; Angew. Chem. Int. Ed. 2006, 45, 4635;
-
(2006)
Angew. Chem. 2006, 118, 4751; Angew. Chem. Int. Ed.
, vol.45
, pp. 4635
-
-
Shibuguchi, T.1
Mihara, H.2
Kuramochi, A.3
Sakuraba, S.4
Ohshima, T.5
Shibasaki, M.6
-
54
-
-
34250648509
-
-
H. Mihara, T. Shibuguchi, A. Kuramochi, T. Ohshima, M. Shibasaki, Heterocycles 2007, 72, 421;
-
(2007)
Heterocycles
, vol.72
, pp. 421
-
-
Mihara, H.1
Shibuguchi, T.2
Kuramochi, A.3
Ohshima, T.4
Shibasaki, M.5
-
55
-
-
66149124126
-
-
Y. -G, Wang, T. Kumano, T. Kano, K. Maruoka, Org. Lett. 2009, 11, 2027;
-
(2009)
Org. Lett.
, vol.11
, pp. 2027
-
-
Wang, Y.-G.1
Kumano, T.2
Kano, T.3
Maruoka, K.4
-
56
-
-
77958195698
-
-
B. Lygo, C. Beynon, M. C. McLeod, C.-E. Roy, C. E. Wade, Tetrahedron 2010, 66, 8832.
-
(2010)
Tetrahedron
, vol.66
, pp. 8832
-
-
Lygo, B.1
Beynon, C.2
McLeod, M.C.3
Roy, C.-E.4
Wade, C.E.5
-
57
-
-
84862750922
-
-
Preliminary communication
-
Preliminary communication: S. Shirakawa, Y. Liu, A. Usui, K. Maruoka, ChemCatChem 2012, 4, 980.
-
(2012)
ChemCatChem
, vol.4
, pp. 980
-
-
Shirakawa, S.1
Liu, Y.2
Usui, A.3
Maruoka, K.4
-
58
-
-
84899875268
-
-
For representative examples of asymmetric conjugate addition of glycine ester under phase-transfer conditions,
-
For representative examples of asymmetric conjugate addition of glycine ester under phase-transfer conditions, see:
-
-
-
-
59
-
-
0032560703
-
-
E. J. Corey, M. C. Noe, F. Xu, Tetrahedron Lett. 1998, 39, 5347;
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5347
-
-
Corey, E.J.1
Noe, M.C.2
Xu, F.3
-
60
-
-
0035902407
-
-
M. J. O'Donnell, F. Delgado, E. Domínguez, J. deBlas, W. L. Scott, Tetrahedron: Asymmetry 2001, 12, 821;
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 821
-
-
O'Donnell, M.J.1
Delgado, F.2
Domínguez, E.3
deBlas, J.4
Scott, W.L.5
-
61
-
-
0037164617
-
-
S. Arai, R. Tsuji, A. Nishida, Tetrahedron Lett. 2002, 43, 9535;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9535
-
-
Arai, S.1
Tsuji, R.2
Nishida, A.3
-
62
-
-
0037963684
-
-
T. Akiyama, M. Hara, K. Fuchibe, S. Sakamoto, K. Yamaguchi, Chem. Commun. 2003, 1734;
-
(2003)
Chem. Commun.
, pp. 1734
-
-
Akiyama, T.1
Hara, M.2
Fuchibe, K.3
Sakamoto, S.4
Yamaguchi, K.5
-
63
-
-
3843123354
-
-
T. Ohshima, T. Shibuguchi, Y. Fukuta, M. Shibasaki, Tetrahedron 2004, 60, 7743;
-
(2004)
Tetrahedron
, vol.60
, pp. 7743
-
-
Ohshima, T.1
Shibuguchi, T.2
Fukuta, Y.3
Shibasaki, M.4
-
64
-
-
16544367097
-
-
S. Arai, K. Tokumaru, T. Aoyama, Chem. Pharm. Bull. 2004, 52, 646;
-
(2004)
Chem. Pharm. Bull.
, vol.52
, pp. 646
-
-
Arai, S.1
Tokumaru, K.2
Aoyama, T.3
-
65
-
-
19544379484
-
-
B. Lygo, B. Allbutt, E. H. M. Kirton, Tetrahedron Lett. 2005, 46, 4461;
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 4461
-
-
Lygo, B.1
Allbutt, B.2
Kirton, E.H.M.3
-
66
-
-
78751470236
-
-
M.-Q. Hua, L. Wang, H.-F. Cui, J. Nie, X.-L. Zhang, J.-A. Ma, Chem. Commun. 2011, 47, 1631;
-
(2011)
Chem. Commun.
, vol.47
, pp. 1631
-
-
Hua, M.-Q.1
Wang, L.2
Cui, H.-F.3
Nie, J.4
Zhang, X.-L.5
Ma, J.-A.6
-
67
-
-
79952263142
-
-
T. Ma, X. Fu, C. W. Kee, L. Zong, Y. Pan, K.-W. Huang, C.-H. Tan, J. Am. Chem. Soc. 2011, 133, 2828;
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 2828
-
-
Ma, T.1
Fu, X.2
Kee, C.W.3
Zong, L.4
Pan, Y.5
Huang, K.-W.6
Tan, C.-H.7
-
68
-
-
84858376909
-
-
H. Kawai, Y. Sugita, E. Tokunaga, H. Sato, M. Shiro, N. Shibata, Chem. Commun. 2012, 48, 3632.
-
(2012)
Chem. Commun.
, vol.48
, pp. 3632
-
-
Kawai, H.1
Sugita, Y.2
Tokunaga, E.3
Sato, H.4
Shiro, M.5
Shibata, N.6
-
69
-
-
33846827094
-
-
X. Wang, M. Kitamura, K. Maruoka, J. Am. Chem. Soc. 2007, 129, 1038;
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 1038
-
-
Wang, X.1
Kitamura, M.2
Maruoka, K.3
-
70
-
-
34249906781
-
-
Q. Lan, X. Wang, K. Maruoka, Tetrahedron Lett. 2007, 48, 4675;
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 4675
-
-
Lan, Q.1
Wang, X.2
Maruoka, K.3
-
71
-
-
66149139305
-
-
T. Kano, T. Kumano, K. Maruoka, Org. Lett. 2009, 11, 2023;
-
(2009)
Org. Lett.
, vol.11
, pp. 2023
-
-
Kano, T.1
Kumano, T.2
Maruoka, K.3
-
72
-
-
65549146429
-
-
Q. Lan, X. Wang, R. He, C. Ding, K. Maruoka, Tetrahedron Lett. 2009, 50, 3280;
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 3280
-
-
Lan, Q.1
Wang, X.2
He, R.3
Ding, C.4
Maruoka, K.5
-
73
-
-
77952923651
-
-
Q. Lan, X. Wang, S. Shirakawa, K. Maruoka, Org. Process Res. Dev. 2010, 14, 684;
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 684
-
-
Lan, Q.1
Wang, X.2
Shirakawa, S.3
Maruoka, K.4
-
74
-
-
84860625203
-
-
J. Nie, M.-Q. Hua, H.-Y. Xiong, Y. Zheng, J.-A. Ma, J. Org. Chem. 2012, 77, 4209.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 4209
-
-
Nie, J.1
Hua, M.-Q.2
Xiong, H.-Y.3
Zheng, Y.4
Ma, J.-A.5
-
75
-
-
84899816531
-
-
CCDC877856 contains the supplementary crystallographic data for 1f'. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via
-
CCDC877856 contains the supplementary crystallographic data for 1f'. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
-
-
-
-
76
-
-
0037166006
-
-
G. Srinivasan, C. M. James, J. A. Krzycki, Science 2002, 296, 1459;
-
(2002)
Science
, vol.296
, pp. 1459
-
-
Srinivasan, G.1
James, C.M.2
Krzycki, J.A.3
-
77
-
-
0037165964
-
-
B. Hao, W. Gong, T. K. Ferguson, C. M. James, J. A. Krzycki, M. K. Chan, Science 2002, 296, 1462;
-
(2002)
Science
, vol.296
, pp. 1462
-
-
Hao, B.1
Gong, W.2
Ferguson, T.K.3
James, C.M.4
Krzycki, J.A.5
Chan, M.K.6
-
78
-
-
4644312237
-
-
S. K. Blight, R. C. Larue, A. Mahapatra, D. G. Longstaff, E. Chang, G. Zhao, P. T. Kang, K. B. Green-Church, M. K. Chan, J. A. Krzycki, Nature 2004, 431, 333;
-
(2004)
Nature
, vol.431
, pp. 333
-
-
Blight, S.K.1
Larue, R.C.2
Mahapatra, A.3
Longstaff, D.G.4
Chang, E.5
Zhao, G.6
Kang, P.T.7
Green-Church, K.B.8
Chan, M.K.9
Krzycki, J.A.10
-
79
-
-
79953249251
-
-
M. A. Gaston, L. Zhang, K. B. Green-Church, J. A. Krzycki, Nature 2011, 471, 647.
-
(2011)
Nature
, vol.471
, pp. 647
-
-
Gaston, M.A.1
Zhang, L.2
Green-Church, K.B.3
Krzycki, J.A.4
-
80
-
-
84899885497
-
-
The major diastereomer of 3i was selectively cyclized in the isolation step, and 4i was obtained as a single diastereomer.
-
The major diastereomer of 3i was selectively cyclized in the isolation step, and 4i was obtained as a single diastereomer.
-
-
-
-
81
-
-
4644226332
-
-
B. Hao, G. Zhao, P. T. Kang, J. A. Soares, T. K. Ferguson, J. Gallucci, J. A. Krzycki, M. K. Chan, Chem. Biol. 2004, 11, 1317; see also:
-
(2004)
Chem. Biol.
, vol.11
, pp. 1317
-
-
Hao, B.1
Zhao, G.2
Kang, P.T.3
Soares, J.A.4
Ferguson, T.K.5
Gallucci, J.6
Krzycki, J.A.7
Chan, M.K.8
-
82
-
-
84858663085
-
-
M. L. Wong, I. A. Guzei, L. L. Kiessling, Org. Lett. 2012, 14, 1378.
-
(2012)
Org. Lett.
, vol.14
, pp. 1378
-
-
Wong, M.L.1
Guzei, I.A.2
Kiessling, L.L.3
-
84
-
-
73249135377
-
-
F. Maltais, Y. C. Jung, M. Chen, J. Tanoury, R. B. Perni, N. Mani, L. Laitinen, H. Huang, S. Liao, H. Gao, H. Tsao, E. Block, C. Ma, R. S. Shawgo, C. Town, C. L. Brummel, D. Howe, S. Pazhanisamy, S. Raybuck, M. Namchuk, Y. L. Bennani, J. Med. Chem. 2009, 52, 7993;
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7993
-
-
Maltais, F.1
Jung, Y.C.2
Chen, M.3
Tanoury, J.4
Perni, R.B.5
Mani, N.6
Laitinen, L.7
Huang, H.8
Liao, S.9
Gao, H.10
Tsao, H.11
Block, E.12
Ma, C.13
Shawgo, R.S.14
Town, C.15
Brummel, C.L.16
Howe, D.17
Pazhanisamy, S.18
Raybuck, S.19
Namchuk, M.20
Bennani, Y.L.21
more..
-
85
-
-
77958485628
-
-
A. Znabet, M. M. Polak, E. Janssen, F. J. J. deKanter, N. J. Turner, R. V. A. Orru, E. Ruijter, Chem. Commun. 2010, 46, 7918;
-
(2010)
Chem. Commun.
, vol.46
, pp. 7918
-
-
Znabet, A.1
Polak, M.M.2
Janssen, E.3
deKanter, F.J.J.4
Turner, N.J.5
Orru, R.V.A.6
Ruijter, E.7
-
87
-
-
0033603641
-
-
S. C. Bergmeier, S. L. Fundy, P. P. Seth, Tetrahedron 1999, 55, 8025;
-
(1999)
Tetrahedron
, vol.55
, pp. 8025
-
-
Bergmeier, S.C.1
Fundy, S.L.2
Seth, P.P.3
-
88
-
-
0141627972
-
-
S.-H. Chen, J. Lamar, F. Victor, N. Snyder, R. Johnson, B. A. Heinz, M. Wakulchik, Q. M. Wang, Bioorg. Med. Chem. Lett. 2003, 13, 3531;
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3531
-
-
Chen, S.-H.1
Lamar, J.2
Victor, F.3
Snyder, N.4
Johnson, R.5
Heinz, B.A.6
Wakulchik, M.7
Wang, Q.M.8
-
89
-
-
84899827868
-
-
WO 2008090819
-
T. Hamada, WO 2008090819, 2008.
-
(2008)
-
-
Hamada, T.1
-
90
-
-
77949355247
-
-
Biocatalyzed approach
-
Biocatalyzed approach, see: V. Köhler, K. R. Bailey, A. Znabet, J. Raftery, M. Helliwell, N. J. Turner, Angew. Chem. 2010, 122, 2228; Angew. Chem. Int. Ed. 2010, 49, 2182.
-
(2010)
Angew. Chem. 2010, 122, 2228; Angew. Chem. Int. Ed.
, vol.49
, pp. 2182
-
-
Köhler, V.1
Bailey, K.R.2
Znabet, A.3
Raftery, J.4
Helliwell, M.5
Turner, N.J.6
-
91
-
-
0037473547
-
-
T. Ooi, M. Kameda, K. Maruoka, J. Am. Chem. Soc. 2003, 125, 5139;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5139
-
-
Ooi, T.1
Kameda, M.2
Maruoka, K.3
-
92
-
-
1942469485
-
-
K. Maruoka, E. Tayama, T. Ooi, Proc. Natl. Acad. Sci. USA 2004, 101, 5824;
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 5824
-
-
Maruoka, K.1
Tayama, E.2
Ooi, T.3
-
93
-
-
3843094836
-
-
T. Ooi, M. Kameda, M. Taniguchi, K. Maruoka, J. Am. Chem. Soc. 2004, 126, 9685.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9685
-
-
Ooi, T.1
Kameda, M.2
Taniguchi, M.3
Maruoka, K.4
-
94
-
-
84899836663
-
-
When catalyst (S,S)-9c was applied to the reaction in Scheme4, the product 4i was obtained in 68% yield, 50% ee.
-
When catalyst (S, S)-9c was applied to the reaction in Scheme4, the product 4i was obtained in 68% yield, -50% ee.
-
-
-
-
95
-
-
84899812849
-
-
2H. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via
-
2H. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
-
-
-
-
97
-
-
84899853215
-
-
WO 2008053300
-
M. J. Meyers, G. B. Arhancet, X. Chen, S. L. Hockerman, S. A. Long, M. W. Mahoney, D. B. Reitz, J. G. Rico, WO 2008053300, 2008.
-
(2008)
-
-
Meyers, M.J.1
Arhancet, G.B.2
Chen, X.3
Hockerman, S.L.4
Long, S.A.5
Mahoney, M.W.6
Reitz, D.B.7
Rico, J.G.8
-
98
-
-
79961241357
-
-
S. Lin, L. Deiana, G.-L. Zhao, J. Sun, A. Córdova, Angew. Chem. 2011, 123, 7766; Angew. Chem. Int. Ed. 2011, 50, 7624.
-
(2011)
Angew. Chem. 2011, 123, 7766; Angew. Chem. Int. Ed.
, vol.50
, pp. 7624
-
-
Lin, S.1
Deiana, L.2
Zhao, G.-L.3
Sun, J.4
Córdova, A.5
-
99
-
-
12144286493
-
-
R. B. Perni, L. J. Farmer, K. M. Cottrell, J. J. Court, L. F. Courtney, D. D. Deininger, C. A. Gates, S. L. Harbeson, J. L. Kim, C. Lin, K. Lin, Y.-P. Luong, J. P. Maxwell, M. A. Murcko, J. Pitlik, B. G. Rao, W. C. Schairer, R. D. Tung, J. H. VanDrie, K. Wilson, J. A. Thomson, Bioorg. Med. Chem. Lett. 2004, 14, 1939.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1939
-
-
Perni, R.B.1
Farmer, L.J.2
Cottrell, K.M.3
Court, J.J.4
Courtney, L.F.5
Deininger, D.D.6
Gates, C.A.7
Harbeson, S.L.8
Kim, J.L.9
Lin, C.10
Lin, K.11
Luong, Y.-P.12
Maxwell, J.P.13
Murcko, M.A.14
Pitlik, J.15
Rao, B.G.16
Schairer, W.C.17
Tung, R.D.18
VanDrie, J.H.19
Wilson, K.20
Thomson, J.A.21
more..
-
100
-
-
84899796751
-
-
After the reaction, catalyst (S,S)-9c could be recovered (ca.80%) by column chromatography and reused without loss of activity.
-
After the reaction, catalyst (S, S)-9c could be recovered (ca.80%) by column chromatography and reused without loss of activity.
-
-
-
|