-
1
-
-
33749821128
-
-
For a summary of the early isolations of various Securinega alkaloids, see: "The Securinega Alkaloids": in (Ed.: R.H.F. Manske), . Intriguingly, compounds 1 and 2 are enantiomeric and have been isolated as single antipodes from their producing organisms. For an interesting review on enantiomeric natural products, see
-
For a summary of the early isolations of various Securinega alkaloids, see: "The Securinega Alkaloids":, V. Snieckus, in The Alkaloids, Vol.14 (Ed.:, R.H.F. Manske,), 1975, pp. 425-506. Intriguingly, compounds 1 and 2 are enantiomeric and have been isolated as single antipodes from their producing organisms. For an interesting review on enantiomeric natural products, see
-
(1975)
The Alkaloids, Vol.14
, pp. 425-506
-
-
Snieckus, V.1
-
2
-
-
84878043273
-
-
J. M. Finefield, D. H. Sherman, M. Kreitman, R. M. Williams, Angew. Chem. 2012, 124, 4886-4920
-
(2012)
Angew. Chem.
, vol.124
, pp. 4886-4920
-
-
Finefield, J.M.1
Sherman, D.H.2
Kreitman, M.3
Williams, R.M.4
-
3
-
-
84860854183
-
-
Angew. Chem. Int. Ed. 2012, 51, 4802-4836.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 4802-4836
-
-
-
4
-
-
0037424771
-
-
A. Ohsaki, H. Ishiyama, K. Yoneda, J. Kobayashi, Tetrahedron Lett. 2003, 44, 3097-3099.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3097-3099
-
-
Ohsaki, A.1
Ishiyama, H.2
Yoneda, K.3
Kobayashi, J.4
-
5
-
-
84862588022
-
-
B.-X. Zhao, Y. Wang, D.-M. Zhang, X.-J. Huang, L.-L. Bai, Y. Yan, J.-M. Chen, T.-B. Lu, Y.-T. Wang, Q.-W. Zhang, W.-C. Ye, Org. Lett. 2012, 14, 3096-3099.
-
(2012)
Org. Lett.
, vol.14
, pp. 3096-3099
-
-
Zhao, B.-X.1
Wang, Y.2
Zhang, D.-M.3
Huang, X.-J.4
Bai, L.-L.5
Yan, Y.6
Chen, J.-M.7
Lu, T.-B.8
Wang, Y.-T.9
Zhang, Q.-W.10
Ye, W.-C.11
-
6
-
-
0023549451
-
-
For studies of the GABA activity of securinine, see
-
J. A. Beutler, A. N. Brubaker, Drugs Future 1987, 12, 957-976. For studies of the GABA activity of securinine, see
-
(1987)
Drugs Future
, vol.12
, pp. 957-976
-
-
Beutler, J.A.1
Brubaker, A.N.2
-
7
-
-
0026772112
-
-
D. Rognan, T. Boulanger, R. Hoffmann, D. P. Vercauteren, J.-M. Andre, F. Durant, C.-G. Wermuth, J. Med. Chem. 1992, 35, 1969-1977
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1969-1977
-
-
Rognan, D.1
Boulanger, T.2
Hoffmann, R.3
Vercauteren, D.P.4
Andre, J.-M.5
Durant, F.6
Wermuth, C.-G.7
-
8
-
-
0028886410
-
-
For studies of other biological activities, see
-
E. Galvez-Ruano, M. H. Aprison, D. H. Robertson, K. B. Lipkowitz, J. Neurosci. Res. 1995, 42, 666-673. For studies of other biological activities, see
-
(1995)
J. Neurosci. Res.
, vol.42
, pp. 666-673
-
-
Galvez-Ruano, E.1
Aprison, M.H.2
Robertson, D.H.3
Lipkowitz, K.B.4
-
9
-
-
0025175365
-
-
H. Weenen, M. H. H. Nkunya, D. H. Bray, L. B. Mwasumbi, L. S. Kinabo, V. A. Kilimali, J. B. Wijnberg, Planta Med. 1990, 56, 371-373
-
(1990)
Planta Med.
, vol.56
, pp. 371-373
-
-
Weenen, H.1
Nkunya, M.H.H.2
Bray, D.H.3
Mwasumbi, L.B.4
Kinabo, L.S.5
Kilimali, V.A.6
Wijnberg, J.B.7
-
10
-
-
0025159251
-
-
J. L. Mensah, I. Lagarde, C. Ceschin, G. Michael, J. Gleye, I. Fouraste, J. Ethnopharmacol. 1990, 28, 129-133
-
(1990)
J. Ethnopharmacol.
, vol.28
, pp. 129-133
-
-
Mensah, J.L.1
Lagarde, I.2
Ceschin, C.3
Michael, G.4
Gleye, J.5
Fouraste, I.6
-
11
-
-
0025728312
-
-
H. Tatematsu, M. Mori, T.-H. Yang, J.-J. Chang, T. T.-Y. Lee, K.-H. Lee, J. Pharm. Sci. 1991, 80, 325-327
-
(1991)
J. Pharm. Sci.
, vol.80
, pp. 325-327
-
-
Tatematsu, H.1
Mori, M.2
Yang, T.-H.3
Chang, J.-J.4
Lee, T.T.-Y.5
Lee, K.-H.6
-
12
-
-
13044285433
-
-
N. Z. Dong, Z. L. Gu, W. H. Chou, C. Y. Kwok, Acta Pharmacol. Sin. 1999, 20, 267-270.
-
(1999)
Acta Pharmacol. Sin.
, vol.20
, pp. 267-270
-
-
Dong, N.Z.1
Gu, Z.L.2
Chou, W.H.3
Kwok, C.Y.4
-
13
-
-
0013887785
-
-
S. Saito, H. Yoshikawa, Y. Sato, H. Nakai, N. Sugimoto, Z. Horii, M. Hanaoka, Y. Tamura, Chem. Pharm. Bull. 1966, 14, 313-314
-
(1966)
Chem. Pharm. Bull.
, vol.14
, pp. 313-314
-
-
Saito, S.1
Yoshikawa, H.2
Sato, Y.3
Nakai, H.4
Sugimoto, N.5
Horii, Z.6
Hanaoka, M.7
Tamura, Y.8
-
15
-
-
0024806965
-
-
P. A. Jacobi, C. A. Blum, R. W. DeSimone, U. E. S. Udong, Tetrahedron Lett. 1989, 30, 7173-7176
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 7173-7176
-
-
Jacobi, P.A.1
Blum, C.A.2
Desimone, R.W.3
Udong, U.E.S.4
-
16
-
-
0001421951
-
-
P. A. Jacobi, C. A. Blum, R. W. DeSimone, U. E. S. Dong, J. Am. Chem. Soc. 1991, 113, 5384-5392
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 5384-5392
-
-
Jacobi, P.A.1
Blum, C.A.2
Desimone, R.W.3
Dong, U.E.S.4
-
17
-
-
0007101449
-
-
G. Han, M. G. LaPorte, J. J. Folmer, K. M. Werner, S. M. Weinreb, Angew. Chem. 2000, 112, 243-246
-
(2000)
Angew. Chem.
, vol.112
, pp. 243-246
-
-
Han, G.1
Laporte, M.G.2
Folmer, J.J.3
Werner, K.M.4
Weinreb, S.M.5
-
19
-
-
0034613331
-
-
G. Han, M. G. LaPorte, J. J. Folmer, K. M. Werner, S. M. Weinreb, J. Org. Chem. 2000, 65, 6293-6306
-
(2000)
J. Org. Chem.
, vol.65
, pp. 6293-6306
-
-
Han, G.1
Laporte, M.G.2
Folmer, J.J.3
Werner, K.M.4
Weinreb, S.M.5
-
20
-
-
0001594575
-
-
G. Han, M. G. LaPorte, M. C. McIntosh, S. M. Weinreb, J. Org. Chem. 1996, 61, 9483-9493
-
(1996)
J. Org. Chem.
, vol.61
, pp. 9483-9493
-
-
Han, G.1
Laporte, M.G.2
McIntosh, M.C.3
Weinreb, S.M.4
-
21
-
-
0034729972
-
-
T. Honda, H. Namiki, M. Kudoh, N. Wantanabe, H. Nagase, H. Mizutani, Tetrahedron Lett. 2000, 41, 5927-5930
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 5927-5930
-
-
Honda, T.1
Namiki, H.2
Kudoh, M.3
Wantanabe, N.4
Nagase, H.5
Mizutani, H.6
-
22
-
-
0037226378
-
-
T. Honda, H. Namiki, M. Kudoh, H. Nagase, H. Mizutani, Heterocycles 2003, 59, 169-187
-
(2003)
Heterocycles
, vol.59
, pp. 169-187
-
-
Honda, T.1
Namiki, H.2
Kudoh, M.3
Nagase, H.4
Mizutani, H.5
-
23
-
-
0035826385
-
-
S. Liras, J. E. Davoren, J. Bordner, Org. Lett. 2001, 3, 703-706
-
(2001)
Org. Lett.
, vol.3
, pp. 703-706
-
-
Liras, S.1
Davoren, J.E.2
Bordner, J.3
-
24
-
-
0742304181
-
-
T. Honda, H. Namiki, K. Kaneda, H. Mizutani, Org. Lett. 2004, 6, 87-89
-
(2004)
Org. Lett.
, vol.6
, pp. 87-89
-
-
Honda, T.1
Namiki, H.2
Kaneda, K.3
Mizutani, H.4
-
25
-
-
2942553023
-
-
T. Honda, H. Namiki, N. Watanabe, H. Mizutani, Tetrahedron Lett. 2004, 45, 5211-5213
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 5211-5213
-
-
Honda, T.1
Namiki, H.2
Watanabe, N.3
Mizutani, H.4
-
26
-
-
2942534934
-
-
R. Alibés, M. Ballbe, F. Busqué, P. deMarch, L. Elias, M. Figueredo, J. Font, Org. Lett. 2004, 6, 1813-1816
-
(2004)
Org. Lett.
, vol.6
, pp. 1813-1816
-
-
Alibés, R.1
Ballbe, M.2
Busqué, F.3
Demarch, P.4
Elias, L.5
Figueredo, M.6
Font, J.7
-
27
-
-
27644536211
-
-
R. Alibés, P. Bayon, P. deMarch, M. Figueredo, J. Font, E. Garcia-Garcia, D. Gonzalez-Galvez, Org. Lett. 2005, 7, 5107-5109
-
(2005)
Org. Lett.
, vol.7
, pp. 5107-5109
-
-
Alibés, R.1
Bayon, P.2
Demarch, P.3
Figueredo, M.4
Font, J.5
Garcia-Garcia, E.6
Gonzalez-Galvez, D.7
-
29
-
-
33749858163
-
-
Angew. Chem. Int. Ed. 2006, 45, 6560-6563
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6560-6563
-
-
-
31
-
-
54749144499
-
-
Angew. Chem. Int. Ed. 2008, 47, 7945-7948
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7945-7948
-
-
-
32
-
-
0037484718
-
-
F. Busqué, M. Canto, P. deMarch, M. Figueredo, J. Font, Tetrahedron: Asymmetry 2003, 14, 2021-2032
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 2021-2032
-
-
Busqué, F.1
Canto, M.2
Demarch, P.3
Figueredo, M.4
Font, J.5
-
33
-
-
45249097976
-
-
P. Liu, S. Hong, S. M. Weinreb, J. Am. Chem. Soc. 2008, 130, 7562-7563
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7562-7563
-
-
Liu, P.1
Hong, S.2
Weinreb, S.M.3
-
34
-
-
58149464323
-
-
B. Dhudshia, B. F. T. Cooper, C. L. B. Macdonald, A. N. Thadani, Chem. Commun. 2009, 463-465
-
(2009)
Chem. Commun.
, pp. 463-465
-
-
Dhudshia, B.1
Cooper, B.F.T.2
Macdonald, C.L.B.3
Thadani, A.N.4
-
36
-
-
84866020610
-
-
J.-H. Chen, S. R. Levine, J. F. Buergler, T. C. McMahon, M. R. Medeiros, J. L. Wood, Org. Lett. 2012, 14, 4531-4533
-
(2012)
Org. Lett.
, vol.14
, pp. 4531-4533
-
-
Chen, J.-H.1
Levine, S.R.2
Buergler, J.F.3
McMahon, T.C.4
Medeiros, M.R.5
Wood, J.L.6
-
38
-
-
81355151524
-
-
M. Sampath, P.-Y. B. Lee, T.-P. Loh, Chem. Sci. 2011, 2, 1988-1991
-
(2011)
Chem. Sci.
, vol.2
, pp. 1988-1991
-
-
Sampath, M.1
Lee, P.-Y.B.2
Loh, T.-P.3
-
39
-
-
84887319017
-
-
H. Wei, C. Qiao, G. Liu, Z. Yang, C.-c. Li, Angew. Chem. 2013, 125, 648-652
-
(2013)
Angew. Chem.
, vol.125
, pp. 648-652
-
-
Wei, H.1
Qiao, C.2
Liu, G.3
Yang, Z.4
-
41
-
-
81255211331
-
-
A. T. Biju, N. Kuhl, F. Glorius, Acc. Chem. Res. 2011, 44, 1182-1195
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 1182-1195
-
-
Biju, A.T.1
Kuhl, N.2
Glorius, F.3
-
42
-
-
80051783520
-
-
N-Heterocyclic Carbenes: From Laboratory Curiosities to Efficient Synthetic Tools":, in (Ed.: S. Díez-González), Royal Society of Chemistry, Cambridge
-
"N-Heterocyclic Carbenes: From Laboratory Curiosities to Efficient Synthetic Tools":, P.-C. Chiang, J. W. Bode, in RSC Catalysis Series (Ed.:, S. Díez-González,), Royal Society of Chemistry, Cambridge, 2010, pp. 339-445
-
(2010)
RSC Catalysis Series
, pp. 339-445
-
-
Chiang, P.-C.1
Bode, J.W.2
-
43
-
-
79956273127
-
-
N-Heterocyclic Carbenes in Organocatalysis":, in (Ed.: C.S.J. Cazin), Springer, Dortrecht
-
"N-Heterocyclic Carbenes in Organocatalysis":, C. D. Campbell, K. B. Ling, A. D. Smith, in N-Heterocyclic Carbenes in Transition Metal Catalysis and Organocatalysis, Catalysis by Metal Complexes, Vol.32 (Ed.:, C.S.J. Cazin,), Springer, Dortrecht, 2011, pp. 263-297
-
(2011)
N-Heterocyclic Carbenes in Transition Metal Catalysis and Organocatalysis, Catalysis by Metal Complexes, Vol.32
, pp. 263-297
-
-
Campbell, C.D.1
Ling, K.B.2
Smith, A.D.3
-
45
-
-
77950278547
-
-
E. M. Phillips, A. Chan, K. A. Scheidt, Aldrichimica Acta 2009, 42, 55-66
-
(2009)
Aldrichimica Acta
, vol.42
, pp. 55-66
-
-
Phillips, E.M.1
Chan, A.2
Scheidt, K.A.3
-
46
-
-
56549104231
-
-
V. Nair, S. Vellalath, B. P. Babu, Chem. Soc. Rev. 2008, 37, 2691-2698
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 2691-2698
-
-
Nair, V.1
Vellalath, S.2
Babu, B.P.3
-
47
-
-
38349109278
-
-
D. Enders, O. Niemeier, A. Henseler, Chem. Rev. 2007, 107, 5606-5655
-
(2007)
Chem. Rev.
, vol.107
, pp. 5606-5655
-
-
Enders, D.1
Niemeier, O.2
Henseler, A.3
-
48
-
-
36549003584
-
-
N. Marion, S. Díez-González, S. P. Nolan, Angew. Chem. 2007, 119, 3046-3058
-
(2007)
Angew. Chem.
, vol.119
, pp. 3046-3058
-
-
Marion, N.1
Díez-González, S.2
Nolan, S.P.3
-
49
-
-
34250870731
-
-
Angew. Chem. Int. Ed. 2007, 46, 2988-3000
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 2988-3000
-
-
-
51
-
-
84874270779
-
-
For a recent review of the use of NHCs in the context of total synthesis, see
-
For a recent review of the use of NHCs in the context of total synthesis, see:, J. Izquierdo, G. E. Hutson, D. T. Cohen, K. A. Scheidt, Angew. Chem. 2012, 124, 11854-11866
-
(2012)
Angew. Chem.
, vol.124
, pp. 11854-11866
-
-
Izquierdo, J.1
Hutson, G.E.2
Cohen, D.T.3
Scheidt, K.A.4
-
52
-
-
84869460648
-
-
Angew. Chem. Int. Ed. 2012, 51, 11686-11698.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 11686-11698
-
-
-
55
-
-
77954281480
-
-
J. Kaeobamrung, J. Mahatthananchai, P. Zheng, J. W. Bode, J. Am. Chem. Soc. 2010, 132, 8810-8812
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8810-8812
-
-
Kaeobamrung, J.1
Mahatthananchai, J.2
Zheng, P.3
Bode, J.W.4
-
57
-
-
79960519557
-
-
Z. Q. Zhu, X.-L. Feng, N.-F. Jiang, X. Wan, J.-C. Xiao, Chem. Commun. 2011, 47, 8670-8672
-
(2011)
Chem. Commun.
, vol.47
, pp. 8670-8672
-
-
Zhu, Z.Q.1
Feng, X.-L.2
Jiang, N.-F.3
Wan, X.4
Xiao, J.-C.5
-
58
-
-
84863338189
-
-
Y.-M. Zhao, Y. Tam, Y.-J. Wang, Z. Li, J. Sun, Org. Lett. 2012, 14, 1398-1401
-
(2012)
Org. Lett.
, vol.14
, pp. 1398-1401
-
-
Zhao, Y.-M.1
Tam, Y.2
Wang, Y.-J.3
Li, Z.4
Sun, J.5
-
59
-
-
84863230138
-
-
D. Du, Z. Hu, J. Jin, Y. Lu, W. Tang, B. Wang, T. Lu, Org. Lett. 2012, 14, 1274-1277
-
(2012)
Org. Lett.
, vol.14
, pp. 1274-1277
-
-
Du, D.1
Hu, Z.2
Jin, J.3
Lu, Y.4
Tang, W.5
Wang, B.6
Lu, T.7
-
60
-
-
84859571449
-
-
J. Mahatthananchai, J. Kaeobamrung, J. W. Bode, ACS Catal. 2012, 2, 494-503.
-
(2012)
ACS Catal.
, vol.2
, pp. 494-503
-
-
Mahatthananchai, J.1
Kaeobamrung, J.2
Bode, J.W.3
-
62
-
-
22144480983
-
-
Interestingly, the mesityl-substituted derivative of 14 (a catalyst designed to prefer homoenolate addition) was no more effective than 14 in our reactions
-
M. S. Kerr, J. R. deAlaniz, T. Rovis, J. Org. Chem. 2005, 70, 5725-5728. Interestingly, the mesityl-substituted derivative of 14 (a catalyst designed to prefer homoenolate addition) was no more effective than 14 in our reactions.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 5725-5728
-
-
Kerr, M.S.1
Dealaniz, J.R.2
Rovis, T.3
-
63
-
-
77956041225
-
-
For the original disclosure, see:, For subsequent disclosures and a review of NHC/Lewis acid cooperative catalysis, see Ref.[6i], and references therein
-
For the original disclosure, see:, D. E. A. Raup, B. Cardinal-David, D. Holte, K. A. Scheidt, Nat. Chem. 2010, 2, 766-771. For subsequent disclosures and a review of NHC/Lewis acid cooperative catalysis, see Ref.[6i], and references therein.
-
(2010)
Nat. Chem.
, vol.2
, pp. 766-771
-
-
Raup, D.E.A.1
Cardinal-David, B.2
Holte, D.3
Scheidt, K.A.4
-
66
-
-
0035477197
-
-
Interestingly, imidazolium pre-catalysts were ineffective in the absence of an exogenous base
-
S. Yamasaki, M. Kanai, M. Shibasaki, Chem. Eur. J. 2001, 7, 4066-4072. Interestingly, imidazolium pre-catalysts were ineffective in the absence of an exogenous base.
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 4066-4072
-
-
Yamasaki, S.1
Kanai, M.2
Shibasaki, M.3
-
70
-
-
84887319269
-
-
P. Magnus, J. Rõdriguez-Lõpez, K. Mulholland, I. Matthews, J. Am. Chem. Soc. 1992, 114, 383-385
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 383-385
-
-
Magnus, P.1
Rõdriguez-Lõpez, J.2
Mulholland, K.3
Matthews, I.4
-
71
-
-
0027201713
-
-
P. Magnus, J. Rõdriguez-Lõpez, K. Mulholland, I. Matthews, Tetrahedron 1993, 49, 8059-8072.
-
(1993)
Tetrahedron
, vol.49
, pp. 8059-8072
-
-
Magnus, P.1
Rõdriguez-Lõpez, J.2
Mulholland, K.3
Matthews, I.4
-
72
-
-
68349095634
-
-
N. Z. Burns, P. S. Baran, R. W. Hoffmann, Angew. Chem. 2009, 121, 2896-2910
-
(2009)
Angew. Chem.
, vol.121
, pp. 2896-2910
-
-
Burns, N.Z.1
Baran, P.S.2
Hoffmann, R.W.3
-
73
-
-
70349769724
-
-
Angew. Chem. Int. Ed. 2009, 48, 2854-2867.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 2854-2867
-
-
-
74
-
-
84875180910
-
-
During the review of this manuscript, a related NHC/Lewis acid catalyst system for the intermolecular homoenolate addition of an ynal to non-enolizable α-keto esters was reported
-
During the review of this manuscript, a related NHC/Lewis acid catalyst system for the intermolecular homoenolate addition of an ynal to non-enolizable α-keto esters was reported:, J. Qi, X. Xie, R. Han, D. Ma, J. Yang, X. She, Chem. Eur. J. 2013, 19, 4146-4150.
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 4146-4150
-
-
Qi, J.1
Xie, X.2
Han, R.3
Ma, D.4
Yang, J.5
She, X.6
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