-
1
-
-
53549121402
-
-
For reviews on organocatalysis, with the emphasis on aminocatalysis, see: (a)
-
For reviews on organocatalysis, with the emphasis on aminocatalysis, see: (a) P. Melchiorre, M. Marigo, M. Carlone, and G. Bartoli Angew. Chem., Int. Ed. 47 2008 6138
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 6138
-
-
Melchiorre, P.1
Marigo, M.2
Carlone, M.3
Bartoli, G.4
-
7
-
-
0036260164
-
-
A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, and K.A. Jørgensen Angew. Chem., Int. Ed. 41 2002 1790
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 1790
-
-
Bøgevig, A.1
Juhl, K.2
Kumaragurubaran, N.3
Zhuang, W.4
Jørgensen, K.A.5
-
12
-
-
0037024190
-
-
N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, and K.A. Jørgensen J. Am. Chem. Soc. 124 2002 6254
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6254
-
-
Kumaragurubaran, N.1
Juhl, K.2
Zhuang, W.3
Bøgevig, A.4
Jørgensen, K.A.5
-
13
-
-
27844576639
-
-
P. Kotrusz, S. Alemayehu, S. Toma, H.-G. Schmalz, and A. Adler Eur. J. Org. Chem. 2005 4904
-
(2005)
Eur. J. Org. Chem.
, pp. 4904
-
-
Kotrusz, P.1
Alemayehu, S.2
Toma, S.3
Schmalz, H.-G.4
Adler, A.5
-
15
-
-
33846037649
-
-
E. Lacoste, E. Vaique, M. Berlande, I. Pianet, J.-M. Vincent, and Y. Landais Eur. J. Org. Chem. 2007 167
-
(2007)
Eur. J. Org. Chem.
, pp. 167
-
-
Lacoste, E.1
Vaique, E.2
Berlande, M.3
Pianet, I.4
Vincent, J.-M.5
Landais, Y.6
-
16
-
-
40149104730
-
-
Y. Hayashi, S. Aratake, Y. Imai, K. Hibino, Q.-Y. Chen, J. Yamaguchi, and T. Uchimaru Chem. Asian J. 3 2008 225
-
(2008)
Chem. Asian J.
, vol.3
, pp. 225
-
-
Hayashi, Y.1
Aratake, S.2
Imai, Y.3
Hibino, K.4
Chen, Q.-Y.5
Yamaguchi, J.6
Uchimaru, T.7
-
17
-
-
34548537133
-
-
T.-Y. Liu, H.-L. Cui, Y. Zhang, K. Jiang, W. Du, Z.-Q. He, and Y.-C. Chen Org. Lett. 9 2007 3671
-
(2007)
Org. Lett.
, vol.9
, pp. 3671
-
-
Liu, T.-Y.1
Cui, H.-L.2
Zhang, Y.3
Jiang, K.4
Du, W.5
He, Z.-Q.6
Chen, Y.-C.7
-
26
-
-
79960848137
-
-
A. Desmarchelier, H. Yalgin, V. Coeffard, X. Moreau, and C. Greck Tetrahedron Lett. 52 2011 4430
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 4430
-
-
Desmarchelier, A.1
Yalgin, H.2
Coeffard, V.3
Moreau, X.4
Greck, C.5
-
28
-
-
79957842272
-
-
J.-Y. Fu, Q.-C. Yang, Q.-L. Wang, J.-N. Ming, F.-Y. Wang, X.-Y. Xu, and L.-X. Wang J. Org. Chem. 76 2011 4661
-
(2011)
J. Org. Chem.
, vol.76
, pp. 4661
-
-
Fu, J.-Y.1
Yang, Q.-C.2
Wang, Q.-L.3
Ming, J.-N.4
Wang, F.-Y.5
Xu, X.-Y.6
Wang, L.-X.7
-
30
-
-
84877719111
-
-
J.-Y. Fu, Q.-L. Wang, L. Peng, Y.-Y. Gui, F. Wang, F. Tian, X.-Y. Xu, and L.-X. Wang Eur. J. Org. Chem. 2013 2864
-
(2013)
Eur. J. Org. Chem.
, pp. 2864
-
-
Fu, J.-Y.1
Wang, Q.-L.2
Peng, L.3
Gui, Y.-Y.4
Wang, F.5
Tian, F.6
Xu, X.-Y.7
Wang, L.-X.8
-
32
-
-
84858633852
-
-
K.L. Jensen, G. Dickmeiss, H. Jiang, L. Albrecht, and K.A. Jørgensen Acc. Chem. Res. 45 2012 248
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 248
-
-
Jensen, K.L.1
Dickmeiss, G.2
Jiang, H.3
Albrecht, L.4
Jørgensen, K.A.5
-
34
-
-
78651382289
-
-
M. Nielsen, D. Worgull, T. Zweifel, B. Gschwend, S. Bertelsen, and K.A. Jørgensen Chem. Commun. 2011 632
-
(2011)
Chem. Commun.
, pp. 632
-
-
Nielsen, M.1
Worgull, D.2
Zweifel, T.3
Gschwend, B.4
Bertelsen, S.5
Jørgensen, K.A.6
-
36
-
-
34250688787
-
-
D. Seebach, A.K. Beck, D.M. Badine, M. Limbach, A. Eschenmoser, A.M. Treasurywala, R. Hobi, W. Prikoszovich, and B. Linder Helv. Chim. Acta 90 2007 425
-
(2007)
Helv. Chim. Acta
, vol.90
, pp. 425
-
-
Seebach, D.1
Beck, A.K.2
Badine, D.M.3
Limbach, M.4
Eschenmoser, A.5
Treasurywala, A.M.6
Hobi, R.7
Prikoszovich, W.8
Linder, B.9
-
38
-
-
84864600742
-
-
Ketals have been shown to undergo non-stereoselective, Lewis acid catalysed α-amination to form α-hydrazino ketals, see
-
Ketals have been shown to undergo non-stereoselective, Lewis acid catalysed α-amination to form α-hydrazino ketals, see: P. Magnus, and A.J. Brozell Org. Lett. 14 2012 3952
-
(2012)
Org. Lett.
, vol.14
, pp. 3952
-
-
Magnus, P.1
Brozell, A.J.2
-
39
-
-
0037424441
-
-
For a selection of Lewis acid and Brønsted acid mediated acetal hydrolysis methods, see: (a)
-
For a selection of Lewis acid and Brønsted acid mediated acetal hydrolysis methods, see: (a) N.S. Krishnaveni, K. Surendra, M.A. Reddy, Y.V.D. Nageswar, and K.R. Rao J. Org. Chem. 68 2003 2018
-
(2003)
J. Org. Chem.
, vol.68
, pp. 2018
-
-
Krishnaveni, N.S.1
Surendra, K.2
Reddy, M.A.3
Nageswar, Y.V.D.4
Rao, K.R.5
-
40
-
-
0142186276
-
-
A. Ates, A. Gautier, B. Leroy, J.-M. Plancher, Y. Quesnel, J.-C. Vanherck, and I.E. Marko Tetrahedron 59 2003 8989
-
(2003)
Tetrahedron
, vol.59
, pp. 8989
-
-
Ates, A.1
Gautier, A.2
Leroy, B.3
Plancher, J.-M.4
Quesnel, Y.5
Vanherck, J.-C.6
Marko, I.E.7
-
41
-
-
10044267850
-
-
J. Sun, Y. Dong, L. Cao, X. Wang, S. Wang, and Y. Hu J. Org. Chem. 69 2004 8932
-
(2004)
J. Org. Chem.
, vol.69
, pp. 8932
-
-
Sun, J.1
Dong, Y.2
Cao, L.3
Wang, X.4
Wang, S.5
Hu, Y.6
-
43
-
-
78049361347
-
-
D.B.G. Williams, A. Cullen, A. Fourie, H. Henning, M. Lawton, W. Mommsen, P. Nangu, J. Parker, and A. Renison Green Chem. 2010 1919 12
-
(1919)
Green Chem.
, vol.2010
, pp. 12
-
-
Williams, D.B.G.1
Cullen, A.2
Fourie, A.3
Henning, H.4
Lawton, M.5
Mommsen, W.6
Nangu, P.7
Parker, J.8
Renison, A.9
-
45
-
-
79953222160
-
-
H. Fujioka, Y. Minamitsuji, O. Kubo, K. Senami, and T. Maegawa Tetrahedron 67 2011 2949
-
(2011)
Tetrahedron
, vol.67
, pp. 2949
-
-
Fujioka, H.1
Minamitsuji, Y.2
Kubo, O.3
Senami, K.4
Maegawa, T.5
-
46
-
-
84855427564
-
-
S. Madabhushi, K.K.R. Mallu, N. Chinthala, C.R. Beeram, and V.S. Vangipuram Tetrahedron Lett. 53 2012 697
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 697
-
-
Madabhushi, S.1
Mallu, K.K.R.2
Chinthala, N.3
Beeram, C.R.4
Vangipuram, V.S.5
-
52
-
-
2942641357
-
-
H. Torii, M. Nakadai, K. Ishihara, S. Saito, and H. Yamamoto Angew. Chem., Int. Ed. 43 2004 1983
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1983
-
-
Torii, H.1
Nakadai, M.2
Ishihara, K.3
Saito, S.4
Yamamoto, H.5
-
58
-
-
54649084880
-
-
J. Zhou, V. Wakchaure, P. Kraft, and B. List Angew. Chem., Int. Ed. 47 2008 7656
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 7656
-
-
Zhou, J.1
Wakchaure, V.2
Kraft, P.3
List, B.4
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