-
1
-
-
0021873440
-
-
K.C. Nicolaou, D.P. Papahatjis, D.A. Claremon, R.L. Magolda, and R.E. Dolle J. Org. Chem. 50 1985 1440 1456
-
(1985)
J. Org. Chem.
, vol.50
, pp. 1440-1456
-
-
Nicolaou, K.C.1
Papahatjis, D.P.2
Claremon, D.A.3
Magolda, R.L.4
Dolle, R.E.5
-
4
-
-
35748940663
-
-
A. Fürstner, M. Bonnekessel, J.T. Blank, K. Radkowski, G. Seidel, F. Lacombe, B. Gabor, and R. Mynott Chem. - Eur. J. 13 2007 8762 8783
-
(2007)
Chem. - Eur. J.
, vol.13
, pp. 8762-8783
-
-
Fürstner, A.1
Bonnekessel, M.2
Blank, J.T.3
Radkowski, K.4
Seidel, G.5
Lacombe, F.6
Gabor, B.7
Mynott, R.8
-
12
-
-
0002782655
-
-
B.M. Trost, I. Fleming, Pergamon Oxford, England
-
D. Caine B.M. Trost, I. Fleming, Comprehensive Organic Synthesis Vol. 3 1991 Pergamon Oxford, England 1 63
-
(1991)
Comprehensive Organic Synthesis
, vol.3
, pp. 1-63
-
-
Caine, D.1
-
23
-
-
0032481358
-
-
M. Yasuda, K. Hayashi, Y. Katoh, I. Shibata, and A. Baba J. Am. Chem. Soc. 120 1998 715 721
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 715-721
-
-
Yasuda, M.1
Hayashi, K.2
Katoh, Y.3
Shibata, I.4
Baba, A.5
-
32
-
-
80054730818
-
-
C. Xing, H. Sun, J. Zhang, G. Li, and Y.R. Chi Chem. - Eur. J. 17 2011 12272 12275
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 12272-12275
-
-
Xing, C.1
Sun, H.2
Zhang, J.3
Li, G.4
Chi, Y.R.5
-
35
-
-
0032560141
-
-
/γ-Alkylation regioselectivity can depend on the leaving group of the alkylation agent
-
α-/γ-Alkylation regioselectivity can depend on the leaving group of the alkylation agent: M.J. Aurell, S. Gil, R. Mestres, M. Parra, and L. Parra Tetrahedron 54 1998 4357 4366
-
(1998)
Tetrahedron
, vol.54
, pp. 4357-4366
-
-
Aurell, M.J.1
Gil, S.2
Mestres, R.3
Parra, M.4
Parra, L.5
-
38
-
-
33947482604
-
-
G. Stork, A. Brizzolara, H. Landesman, J. Szmuszkovicz, and R. Terrell J. Am. Chem. Soc. 85 1963 207 222
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 207-222
-
-
Stork, G.1
Brizzolara, A.2
Landesman, H.3
Szmuszkovicz, J.4
Terrell, R.5
-
44
-
-
36148949559
-
-
B.M. Trost, G.A. Molander, Thieme Stuttgart, Germany
-
T. Sammakia, J.A. Abramite, and M.F. Sammons B.M. Trost, G.A. Molander, Science of Synthesis Vol. 33 2006 Thieme Stuttgart, Germany 405 441
-
(2006)
Science of Synthesis
, vol.33
, pp. 405-441
-
-
Sammakia, T.1
Abramite, J.A.2
Sammons, M.F.3
-
58
-
-
53549095407
-
-
T.E. Müller, K.C. Hultzsch, M. Yus, F. Foubelo, and M. Tada Chem. Rev. 108 2008 3795 3892
-
(2008)
Chem. Rev.
, vol.108
, pp. 3795-3892
-
-
Müller, T.E.1
Hultzsch, K.C.2
Yus, M.3
Foubelo, F.4
Tada, M.5
-
59
-
-
0345098567
-
-
M. Ahmed, A.M. Seayad, R. Jackstell, and M. Beller Angew. Chem., Int. Ed. 42 2003 5615 5619
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 5615-5619
-
-
Ahmed, M.1
Seayad, A.M.2
Jackstell, R.3
Beller, M.4
-
63
-
-
64549085013
-
-
D.M. Hodgson, C.D. Bray, N.D. Kindon, N.J. Reynolds, S.J. Coote, J.M. Um, and K.N. Houk J. Org. Chem. 74 2009 1019 1028
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1019-1028
-
-
Hodgson, D.M.1
Bray, C.D.2
Kindon, N.D.3
Reynolds, N.J.4
Coote, S.J.5
Um, J.M.6
Houk, K.N.7
-
66
-
-
2942585558
-
-
For a review of aza-allylic anion chemistry, see
-
For a review of aza-allylic anion chemistry, see: S. Mangelinckx, N. Giubellina, and N. De Kimpe Chem. Rev. 104 2004 2353 2400
-
(2004)
Chem. Rev.
, vol.104
, pp. 2353-2400
-
-
Mangelinckx, S.1
Giubellina, N.2
De Kimpe, N.3
-
67
-
-
0003882087
-
-
S. Patai, John Wiley & Sons, Ltd. Chichester, UK
-
S. Dayagi, and Y. Degani S. Patai, Carbon-nitrogen Double Bonds 1970 John Wiley & Sons, Ltd. Chichester, UK 64 83
-
(1970)
Carbon-nitrogen Double Bonds
, pp. 64-83
-
-
Dayagi, S.1
Degani, Y.2
-
69
-
-
0037128390
-
-
A. Job, C.F. Janeck, W. Bettray, R. Peters, and D. Enders Tetrahedron 58 2002 2253 2329
-
(2002)
Tetrahedron
, vol.58
, pp. 2253-2329
-
-
Job, A.1
Janeck, C.F.2
Bettray, W.3
Peters, R.4
Enders, D.5
-
70
-
-
77949632348
-
-
For a recent review, see
-
For a recent review, see: R. Lazny, and A. Nodzewska Chem. Rev. 110 2010 1386 1434
-
(2010)
Chem. Rev.
, vol.110
, pp. 1386-1434
-
-
Lazny, R.1
Nodzewska, A.2
-
71
-
-
0034104711
-
-
For a review of methods to recover carbonyl compounds from N,N-dialkylhydrazones, see
-
For a review of methods to recover carbonyl compounds from N,N-dialkylhydrazones, see: D. Enders, L. Wortmann, and R. Peters Acc. Chem. Res. 33 2000 157 169
-
(2000)
Acc. Chem. Res.
, vol.33
, pp. 157-169
-
-
Enders, D.1
Wortmann, L.2
Peters, R.3
-
73
-
-
0002652021
-
-
J.D. Morrison, Academic London, UK
-
D.A. Evans J.D. Morrison, Asymmetric Synthesis Vol. 3 1983 Academic London, UK 1 110
-
(1983)
Asymmetric Synthesis
, vol.3
, pp. 1-110
-
-
Evans, D.A.1
-
75
-
-
0030810476
-
-
A.G. Myers, B.H. Yang, H. Chen, L. McKinstry, D.J. Kopecky, and J.L. Gleason J. Am. Chem. Soc. 119 1997 6496 6511
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 6496-6511
-
-
Myers, A.G.1
Yang, B.H.2
Chen, H.3
McKinstry, L.4
Kopecky, D.J.5
Gleason, J.L.6
-
77
-
-
0001136158
-
-
W. Oppolzer, C. Darcel, P. Rochet, S. Rosset, and J. De Brabander Helv. Chim. Acta 80 1997 1319 1337
-
(1997)
Helv. Chim. Acta
, vol.80
, pp. 1319-1337
-
-
Oppolzer, W.1
Darcel, C.2
Rochet, P.3
Rosset, S.4
De Brabander, J.5
-
86
-
-
0344609024
-
-
J. Košmrlj, L.O. Weigel, D.A. Evans, C.W. Downey, and J. Wu J. Am. Chem. Soc. 125 2003 3208 3209
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3208-3209
-
-
Košmrlj, J.1
Weigel, L.O.2
Evans, D.A.3
Downey, C.W.4
Wu, J.5
-
90
-
-
79952352647
-
-
For β-functionalisation, see:, 10.1038/ncomms1214
-
For β-functionalisation, see: S.-L. Zhang, H.-X. Xie, J. Zhu, H. Li, X.-S. Zhang, J. Li, and W. Wang Nat. Commun. 2 2011 211 10.1038/ncomms1214
-
(2011)
Nat. Commun.
, vol.2
, pp. 211
-
-
Zhang, S.-L.1
Xie, H.-X.2
Zhu, J.3
Li, H.4
Zhang, X.-S.5
Li, J.6
Wang, W.7
-
91
-
-
78650090073
-
-
For γ-functionalisation, see
-
For γ-functionalisation, see: G. Bergonzini, S. Vera, and P. Melchiorre Angew. Chem., Int. Ed. 49 2010 9685 9688
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 9685-9688
-
-
Bergonzini, G.1
Vera, S.2
Melchiorre, P.3
-
92
-
-
84902422003
-
-
E.M. Carreira, H. Yamamoto, Elsevier Amsterdam, Holland
-
D. Uraguchi, and T. Ooi E.M. Carreira, H. Yamamoto, Comprehensive Chirality 2012 Elsevier Amsterdam, Holland 1 36
-
(2012)
Comprehensive Chirality
, pp. 1-36
-
-
Uraguchi, D.1
Ooi, T.2
-
93
-
-
85009278852
-
-
P.I. Dalko, Wiley Weinheim, Germany
-
C. Tran, and P.I. Dalko P.I. Dalko, Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications 2013 Wiley Weinheim, Germany 721 728
-
(2013)
Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications
, pp. 721-728
-
-
Tran, C.1
Dalko, P.I.2
-
94
-
-
85009278852
-
-
P.I. Dalko, Wiley Weinheim, Germany
-
A. Gualandi, D. Petruzziello, E. Emer, and P.G. Cozzi P.I. Dalko, Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications 2013 Wiley Weinheim, Germany 729 756
-
(2013)
Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications
, pp. 729-756
-
-
Gualandi, A.1
Petruzziello, D.2
Emer, E.3
Cozzi, P.G.4
-
95
-
-
85009278852
-
-
P.I. Dalko, Wiley Weinheim, Germany
-
T. Gallavardin, and P.I. Dalko P.I. Dalko, Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications 2013 Wiley Weinheim, Germany 1165 1190
-
(2013)
Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications
, pp. 1165-1190
-
-
Gallavardin, T.1
Dalko, P.I.2
-
101
-
-
84896729343
-
-
Chem. Abstr. 142 2005 429948
-
(2005)
Chem. Abstr.
, vol.142
, pp. 429948
-
-
-
103
-
-
84896701190
-
-
Beeson, T. D.; MacMillan, D. W. C.
-
Beeson, T. D.; MacMillan, D. W. C. Unpublished results, see: http://www.princeton.edu/chemistry/macmillan/research/MacMillan%20Lecture%204. pdf.
-
-
-
-
104
-
-
79954434438
-
-
E. Gómez-Bengoa, A. Landa, A. Lizarraga, A. Mielgo, M. Oiarbide, and C. Palomo Chem. Sci. 2 2011 353 357
-
(2011)
Chem. Sci.
, vol.2
, pp. 353-357
-
-
Gómez-Bengoa, E.1
Landa, A.2
Lizarraga, A.3
Mielgo, A.4
Oiarbide, M.5
Palomo, C.6
-
105
-
-
84855535325
-
-
J. Jiménez, A. Landa, A. Lizarraga, M. Maestro, A. Mielgo, M. Oiarbide, I. Velilla, and C. Palomo J. Org. Chem. 77 2012 747 753
-
(2012)
J. Org. Chem.
, vol.77
, pp. 747-753
-
-
Jiménez, J.1
Landa, A.2
Lizarraga, A.3
Maestro, M.4
Mielgo, A.5
Oiarbide, M.6
Velilla, I.7
Palomo, C.8
-
106
-
-
34447533890
-
-
R. Rios, H. Sundén, J. Vesely, G.-L. Zhao, P. Dziedzic, and A. Córdova Adv. Synth. Catal. 349 2007 1028 1032
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1028-1032
-
-
Rios, R.1
Sundén, H.2
Vesely, J.3
Zhao, G.-L.4
Dziedzic, P.5
Córdova, A.6
-
107
-
-
34848814187
-
-
H. Xie, L. Zu, H. Li, J. Wang, and W. Wang J. Am. Chem. Soc. 129 2007 10886 10894
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 10886-10894
-
-
Xie, H.1
Zu, L.2
Li, H.3
Wang, J.4
Wang, W.5
-
108
-
-
13444267885
-
-
M. Marigo, T.C. Wabnitz, D. Fielenbach, and K.A. Jørgensen Angew. Chem., Int. Ed. 44 2005 794 797
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 794-797
-
-
Marigo, M.1
Wabnitz, T.C.2
Fielenbach, D.3
Jørgensen, K.A.4
-
109
-
-
22144459070
-
-
Y. Hayashi, H. Gotoh, T. Hayashi, and M. Shoji Angew. Chem., Int. Ed. 44 2005 4212 4215
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4212-4215
-
-
Hayashi, Y.1
Gotoh, H.2
Hayashi, T.3
Shoji, M.4
-
113
-
-
55249108726
-
-
R.R. Shaikh, A. Mazzanti, M. Petrini, G. Bartoli, and P. Melchiorre Angew. Chem., Int. Ed. 47 2008 8707 8710
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 8707-8710
-
-
Shaikh, R.R.1
Mazzanti, A.2
Petrini, M.3
Bartoli, G.4
Melchiorre, P.5
-
115
-
-
84876721921
-
-
Y. Zhang, S.-Y. Wang, X.-P. Xu, R. Jiang, and S.-J. Ji Org. Biomol. Chem. 11 2013 1933 1937
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 1933-1937
-
-
Zhang, Y.1
Wang, S.-Y.2
Xu, X.-P.3
Jiang, R.4
Ji, S.-J.5
-
116
-
-
84874440796
-
-
J. Song, C. Guo, A. Adele, H. Yin, and L.-Z. Gong Chem. - Eur. J. 19 2013 3319 3323
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 3319-3323
-
-
Song, J.1
Guo, C.2
Adele, A.3
Yin, H.4
Gong, L.-Z.5
-
118
-
-
84864139952
-
-
Corrigendum, 2012, 18, 10780
-
J. Stiller, A.J. Vorholt, K.A. Ostrowski, A. Behr, and M. Christmann Chem. -Eur. J. 18 2012 9496 9499 Corrigendum, 2012, 18, 10780
-
(2012)
Chem. -Eur. J.
, vol.18
, pp. 9496-9499
-
-
Stiller, J.1
Vorholt, A.J.2
Ostrowski, K.A.3
Behr, A.4
Christmann, M.5
-
121
-
-
80051747006
-
-
A. Gualandi, E. Emer, M.G. Capdevila, and P.G. Cozzi Angew. Chem., Int. Ed. 50 2011 7842 7846
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 7842-7846
-
-
Gualandi, A.1
Emer, E.2
Capdevila, M.G.3
Cozzi, P.G.4
-
123
-
-
80455178516
-
-
X. Tian, C. Cassani, Y. Liu, A. Moran, A. Urakawa, P. Galzerano, E. Arceo, and P. Melchiorre J. Am. Chem. Soc. 133 2011 17934 17941
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 17934-17941
-
-
Tian, X.1
Cassani, C.2
Liu, Y.3
Moran, A.4
Urakawa, A.5
Galzerano, P.6
Arceo, E.7
Melchiorre, P.8
-
124
-
-
77957204396
-
-
M.G. Capdevila, F. Benfatti, L. Zoli, M. Stenta, and P.G. Cozzi Chem. - Eur. J. 16 2010 11237 11241
-
(2010)
Chem. - Eur. J.
, vol.16
, pp. 11237-11241
-
-
Capdevila, M.G.1
Benfatti, F.2
Zoli, L.3
Stenta, M.4
Cozzi, P.G.5
-
125
-
-
84859603084
-
-
J. Xiao Org. Lett. 14 2012 1716 1719
-
(2012)
Org. Lett.
, vol.14
, pp. 1716-1719
-
-
Xiao, J.1
-
126
-
-
84897112850
-
-
M. Guiteras Capdevila, E. Emer, F. Benfatti, A. Gualandi, C.M. Wilson, and P.G. Cozzi Asian J. Org. Chem. 1 2012 38 42
-
(2012)
Asian J. Org. Chem.
, vol.1
, pp. 38-42
-
-
Guiteras Capdevila, M.1
Emer, E.2
Benfatti, F.3
Gualandi, A.4
Wilson, C.M.5
Cozzi, P.G.6
-
127
-
-
79251622073
-
-
E. Emer, R. Sinisi, M.G. Capdevila, D. Petruzziello, F. De Vincentiis, and P.G. Cozzi Eur. J. Org. Chem. 2011 647 666
-
(2011)
Eur. J. Org. Chem.
, pp. 647-666
-
-
Emer, E.1
Sinisi, R.2
Capdevila, M.G.3
Petruzziello, D.4
De Vincentiis, F.5
Cozzi, P.G.6
-
132
-
-
70349684845
-
-
F. Benfatti, M.G. Capdevila, L. Zoli, E. Benedetto, and P.G. Cozzi Chem. Commun. 2009 5919 5921
-
(2009)
Chem. Commun.
, pp. 5919-5921
-
-
Benfatti, F.1
Capdevila, M.G.2
Zoli, L.3
Benedetto, E.4
Cozzi, P.G.5
-
133
-
-
80054729068
-
-
B. Zhang, S.-K. Xiang, L. Zhang, Y. Cui, and N. Jiao Org. Lett. 13 2011 5212 5215
-
(2011)
Org. Lett.
, vol.13
, pp. 5212-5215
-
-
Zhang, B.1
Xiang, S.-K.2
Zhang, L.3
Cui, Y.4
Jiao, N.5
-
135
-
-
84857350578
-
-
For a recent review of synergistic catalysis, see
-
For a recent review of synergistic catalysis, see: A.E. Allen, and D.W.C. MacMillan Chem. Sci. 3 2012 633 658
-
(2012)
Chem. Sci.
, vol.3
, pp. 633-658
-
-
Allen, A.E.1
Macmillan, D.W.C.2
-
136
-
-
84872744548
-
-
For a recent review of methodology combining transition metal catalysis with organocatalysis, see
-
For a recent review of methodology combining transition metal catalysis with organocatalysis, see: Z. Du, and Z. Shao Chem. Soc. Rev. 42 2013 1337 1378
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 1337-1378
-
-
Du, Z.1
Shao, Z.2
-
138
-
-
84857544234
-
-
S. Afewerki, I. Ibrahem, J. Rydfjord, P. Breistein, and A. Córdova Chem. - Eur. J. 18 2012 2972 2977
-
(2012)
Chem. - Eur. J.
, vol.18
, pp. 2972-2977
-
-
Afewerki, S.1
Ibrahem, I.2
Rydfjord, J.3
Breistein, P.4
Córdova, A.5
-
140
-
-
84878387915
-
-
G. Ma, S. Afewerki, L. Deiana, C. Palo-Nieto, L. Liu, J. Sun, I. Ibrahem, and A. Córdova Angew. Chem., Int. Ed. 52 2013 6050 6054
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 6050-6054
-
-
Ma, G.1
Afewerki, S.2
Deiana, L.3
Palo-Nieto, C.4
Liu, L.5
Sun, J.6
Ibrahem, I.7
Córdova, A.8
-
141
-
-
84881172859
-
-
For a diastereoselective intramolecular aldehyde α-allylation using pyrrolidine and Pd(0) co-catalysis in the context of atrop-abyssomicin C total synthesis, see
-
For a diastereoselective intramolecular aldehyde α-allylation using pyrrolidine and Pd(0) co-catalysis in the context of atrop-abyssomicin C total synthesis, see: F. Bihelovic, I. Karadzic, R. Matovic, and R.N. Saicic Org. Biomol. Chem. 11 2013 5413 5424
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 5413-5424
-
-
Bihelovic, F.1
Karadzic, I.2
Matovic, R.3
Saicic, R.N.4
-
142
-
-
84871539856
-
-
For the equivalent of enantioselective intramolecular aldehyde α-allylation using amine and Pd(0) co-catalysis with allenals, see
-
For the equivalent of enantioselective intramolecular aldehyde α-allylation using amine and Pd(0) co-catalysis with allenals, see: M. Li, S. Datta, D.M. Barber, and D.J. Dixon Org. Lett. 14 2012 6350 6353
-
(2012)
Org. Lett.
, vol.14
, pp. 6350-6353
-
-
Li, M.1
Datta, S.2
Barber, D.M.3
Dixon, D.J.4
-
145
-
-
84864487708
-
-
M. Chiarucci, M. di Lillo, A. Romaniello, P.G. Cozzi, G. Cera, and M. Bandini Chem. Sci. 3 2012 2859 2863
-
(2012)
Chem. Sci.
, vol.3
, pp. 2859-2863
-
-
Chiarucci, M.1
Di Lillo, M.2
Romaniello, A.3
Cozzi, P.G.4
Cera, G.5
Bandini, M.6
-
146
-
-
84857033087
-
-
For a recent review on enantioselective propargylic substitution reactions, see
-
For a recent review on enantioselective propargylic substitution reactions, see: Y. Nishibayashi Synthesis 2012 489 503
-
(2012)
Synthesis
, pp. 489-503
-
-
Nishibayashi, Y.1
-
149
-
-
79951613334
-
-
A. Yoshida, M. Ikeda, G. Hattori, Y. Miyake, and Y. Nishibayashi Org. Lett. 13 2011 592 595
-
(2011)
Org. Lett.
, vol.13
, pp. 592-595
-
-
Yoshida, A.1
Ikeda, M.2
Hattori, G.3
Miyake, Y.4
Nishibayashi, Y.5
-
151
-
-
79959445802
-
-
[Absolute configuration of the dominant anti-diastereomer is drawn incorrectly in this paper (although it is correct in the Supplementary data).]
-
R. Sinisi, M.V. Vita, A. Gualandi, E. Emer, and P.G. Cozzi Chem. - Eur. J. 17 2011 7404 7408 [Absolute configuration of the dominant anti-diastereomer is drawn incorrectly in this paper (although it is correct in the Supplementary data).]
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 7404-7408
-
-
Sinisi, R.1
Vita, M.V.2
Gualandi, A.3
Emer, E.4
Cozzi, P.G.5
-
152
-
-
34247565955
-
-
T.D. Beeson, A. Mastracchio, J. Hong, K. Ashton, and D.W.C. MacMillan Science 316 2007 582 585
-
(2007)
Science
, vol.316
, pp. 582-585
-
-
Beeson, T.D.1
Mastracchio, A.2
Hong, J.3
Ashton, K.4
Macmillan, D.W.C.5
-
153
-
-
34247165162
-
-
A contemporaneous report on organocatalytic enantioselective α-oxyamination of aldehydes using TEMPO () was initially proposed to proceed through SOMO activation but has subsequently been shown to operate by a traditional (closed-shell) enamine catalysis pathway with Lewis acid activation of TEMPO, see
-
A contemporaneous report on organocatalytic enantioselective α-oxyamination of aldehydes using TEMPO (M.P. Sibi, and M. Hasegawa J. Am. Chem. Soc. 129 2007 4124 4125) was initially proposed to proceed through SOMO activation but has subsequently been shown to operate by a traditional (closed-shell) enamine catalysis pathway with Lewis acid activation of TEMPO, see
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 4124-4125
-
-
Sibi, M.P.1
Hasegawa, M.2
-
156
-
-
84896695550
-
-
M. Christmann, S. Bräse, Wiley-VCH Weinheim, Germany
-
D.W.C. MacMillan, and S. Rendler M. Christmann, S. Bräse, Asymmetric Synthesis II 2012 Wiley-VCH Weinheim, Germany 87 94
-
(2012)
Asymmetric Synthesis II
, pp. 87-94
-
-
Macmillan, D.W.C.1
Rendler, S.2
-
159
-
-
77956039300
-
-
J.J. Devery III, J.C. Conrad, D.W.C. MacMillan, and R.A. Flowers II Angew. Chem., Int. Ed. 49 2010 6106 6110
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 6106-6110
-
-
Devery III, J.J.1
Conrad, J.C.2
MacMillan, D.W.C.3
Flowers II, R.A.4
-
161
-
-
68849107137
-
-
For a related strategy to β-nitroaldehydes using TIPS nitronates, see
-
For a related strategy to β-nitroaldehydes using TIPS nitronates, see: J.E. Wilson, A.D. Casarez, and D.W.C. MacMillan J. Am. Chem. Soc. 131 2009 11332 11334
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11332-11334
-
-
Wilson, J.E.1
Casarez, A.D.2
Macmillan, D.W.C.3
-
166
-
-
67749114483
-
-
Corrigendum, 2009, 131, 6640
-
K.C. Nicolaou, R. Reingruber, D. Sarlah, and S. Bräse J. Am. Chem. Soc. 131 2009 2086 2087 Corrigendum, 2009, 131, 6640
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2086-2087
-
-
Nicolaou, K.C.1
Reingruber, R.2
Sarlah, D.3
Bräse, S.4
-
168
-
-
34547178180
-
-
J. Alemán, S. Cabrera, E. Maerten, J. Overgaard, and K.A. Jørgensen Angew. Chem., Int. Ed. 46 2007 5520 5523
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 5520-5523
-
-
Alemán, J.1
Cabrera, S.2
Maerten, E.3
Overgaard, J.4
Jørgensen, K.A.5
-
170
-
-
84859748126
-
-
P. Nareddy, L. Mantilli, L. Guénée, and C. Mazet Angew. Chem., Int. Ed. 51 2012 3826 3831
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 3826-3831
-
-
Nareddy, P.1
Mantilli, L.2
Guénée, L.3
Mazet, C.4
-
171
-
-
84864722925
-
-
C. Mazet Synlett 2012 1999 2004
-
(2012)
Synlett
, pp. 1999-2004
-
-
Mazet, C.1
-
173
-
-
77950849290
-
-
For enamine SOMO-initiated aryl-teminated polyene cyclisations, see
-
For enamine SOMO-initiated aryl-teminated polyene cyclisations, see: S. Rendler, and D.W.C. MacMillan J. Am. Chem. Soc. 132 2010 5027 5029
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 5027-5029
-
-
Rendler, S.1
Macmillan, D.W.C.2
-
175
-
-
84880124916
-
-
For a recent review of applications of photoredox catalysis using transition metal complexes in organic chemistry, see
-
For a recent review of applications of photoredox catalysis using transition metal complexes in organic chemistry, see: C.K. Prier, D.A. Rankic, and D.W.C. MacMillan Chem. Rev. 113 2013 5322 5363
-
(2013)
Chem. Rev.
, vol.113
, pp. 5322-5363
-
-
Prier, C.K.1
Rankic, D.A.2
Macmillan, D.W.C.3
-
176
-
-
78751510344
-
-
M. Neumann, S. Füldner, B. König, and K. Zeitler Angew. Chem., Int. Ed. 50 2011 951 954
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 951-954
-
-
Neumann, M.1
Füldner, S.2
König, B.3
Zeitler, K.4
-
178
-
-
84860449806
-
-
K. Fidaly, C. Ceballos, A. Falguières, M.S.-I. Veitia, A. Guy, and C. Ferroud Green Chem. 14 2012 1293 1297
-
(2012)
Green Chem.
, vol.14
, pp. 1293-1297
-
-
Fidaly, K.1
Ceballos, C.2
Falguières, A.3
Veitia, M.S.-I.4
Guy, A.5
Ferroud, C.6
-
179
-
-
84859937539
-
-
M. Cherevatskaya, M. Neumann, S. Füldner, C. Harlander, S. Kümmel, S. Dankesreiter, A. Pfitzner, K. Zeitler, and B. König Angew. Chem., Int. Ed. 51 2012 4062 4066
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 4062-4066
-
-
Cherevatskaya, M.1
Neumann, M.2
Füldner, S.3
Harlander, C.4
Kümmel, S.5
Dankesreiter, S.6
Pfitzner, A.7
Zeitler, K.8
König, B.9
-
180
-
-
84866389262
-
-
P. Wu, C. He, J. Wang, X. Peng, X. Li, Y. An, and C. Duan J. Am. Chem. Soc. 134 2012 14991 14999
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 14991-14999
-
-
Wu, P.1
He, C.2
Wang, J.3
Peng, X.4
Li, X.5
An, Y.6
Duan, C.7
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