-
1
-
-
84944053662
-
-
in, (Eds., A. R. Katritzky, C. W. Rees, E. F. V. Scriven, Pergamon Press, Oxford
-
G. Jones in Comprehensive Heterocyclic Chemistry II, (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon Press, Oxford, UK, 1996, pp. 167–243;
-
(1996)
Comprehensive Heterocyclic Chemistry II
, pp. 167-243
-
-
Jones, G.1
-
2
-
-
0029154248
-
-
J. Semba, A. Watanabe, S. Kito, M. Toru, Neuropharmacology 1995, 34, 785;
-
(1995)
Neuropharmacology
, vol.34
, pp. 785
-
-
Semba, J.1
Watanabe, A.2
Kito, S.3
Toru, M.4
-
3
-
-
0027008374
-
-
H. Hayashi, Y. Miwa, I. Miki, S. Ichikawa, N. Yoda, A. Ishii, M. Kono, F. Suzuki, J. Med. Chem. 1992, 35, 4893;
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4893
-
-
Hayashi, H.1
Miwa, Y.2
Miki, I.3
Ichikawa, S.4
Yoda, N.5
Ishii, A.6
Kono, M.7
Suzuki, F.8
-
4
-
-
0033813482
-
-
H. Zhao, A. Thurkauf, J. Braun, R. Brodbeck, A. Kieltyka, Bioorg. Med. Chem. Lett. 2000, 10, 2119;
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2119
-
-
Zhao, H.1
Thurkauf, A.2
Braun, J.3
Brodbeck, R.4
Kieltyka, A.5
-
5
-
-
0035939374
-
-
M. Patel, R. J. McHugh, B. C. Cordova, R. M. Klabe, L. T. Bacheler, S. Erickson-Viitanen, J. D. Rodgers, Bioorg. Med. Chem. Lett. 2001, 11, 1943;
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1943
-
-
Patel, M.1
McHugh, R.J.2
Cordova, B.C.3
Klabe, R.M.4
Bacheler, L.T.5
Erickson-Viitanen, S.6
Rodgers, J.D.7
-
6
-
-
29444458698
-
-
R. Uchida, R. Imasoto, K. Shiomi, H. Tomoda, S. Omura, Org. Lett. 2005, 7, 5701.
-
(2005)
Org. Lett.
, vol.7
, pp. 5701
-
-
Uchida, R.1
Imasoto, R.2
Shiomi, K.3
Tomoda, H.4
Omura, S.5
-
7
-
-
85020558015
-
-
For selected examples for the synthesis of 3,4-dihydroquinolin-2-ones, s
-
For selected examples for the synthesis of 3,4-dihydroquinolin-2-ones, see:
-
-
-
-
8
-
-
31544481150
-
-
K. L. Turner, T. M. Baker, S. Islam, D. J. Procter, M. Stefaniak, Org. Lett. 2006, 8, 329;
-
(2006)
Org. Lett.
, vol.8
, pp. 329
-
-
Turner, K.L.1
Baker, T.M.2
Islam, S.3
Procter, D.J.4
Stefaniak, M.5
-
9
-
-
59249099229
-
-
W. Zhou, L. R. Zhang, N. Jiao, Tetrahedron 2009, 65, 1982;
-
(2009)
Tetrahedron
, vol.65
, pp. 1982
-
-
Zhou, W.1
Zhang, L.R.2
Jiao, N.3
-
10
-
-
84892969930
-
-
B. Li, Y. Park, S. Chang, J. Am. Chem. Soc. 2014, 136, 1125;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 1125
-
-
Li, B.1
Park, Y.2
Chang, S.3
-
11
-
-
84908066004
-
-
O. D. Engl, S. P. Fritz, Al. Käslin, H. Wennemers, Org. Lett. 2014, 16, 5454;
-
(2014)
Org. Lett.
, vol.16
, pp. 5454
-
-
Engl, O.D.1
Fritz, S.P.2
Käslin, A.3
Wennemers, H.4
-
12
-
-
84899896529
-
-
J. X. Yan, H. Li, X. W. Liu, J. L. Shi, X. Wang, Z. J. Shi, Angew. Chem. Int. Ed. 2014, 53, 4945;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 4945
-
-
Yan, J.X.1
Li, H.2
Liu, X.W.3
Shi, J.L.4
Wang, X.5
Shi, Z.J.6
-
13
-
-
84973338819
-
-
Angew. Chem. 2014, 126, 5045;
-
(2014)
Angew. Chem.
, vol.126
, pp. 5045
-
-
-
14
-
-
84902348370
-
-
Z. Q. Fu, K. Jiang, T. S. Zhu, J. Torres, Y. G. R. Chi, Angew. Chem. Int. Ed. 2014, 53, 6506;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 6506
-
-
Fu, Z.Q.1
Jiang, K.2
Zhu, T.S.3
Torres, J.4
Chi, Y.G.R.5
-
15
-
-
84935035797
-
-
Angew. Chem. 2014, 126, 6624;
-
(2014)
Angew. Chem.
, vol.126
, pp. 6624
-
-
-
16
-
-
84922784373
-
-
S. R. Vidadala, C. Golz, C. Strohmann, C.-G. Daniliuc, H. Waldmann, Angew. Chem. Int. Ed. 2015, 54, 651;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 651
-
-
Vidadala, S.R.1
Golz, C.2
Strohmann, C.3
Daniliuc, C.-G.4
Waldmann, H.5
-
17
-
-
85027041242
-
-
Angew. Chem. 2015, 127, 661;
-
(2015)
Angew. Chem.
, vol.127
, pp. 661
-
-
-
18
-
-
85006410194
-
-
Y. Zhao, J. R. Chen, W. J. Xiao, Org. Lett. 2016, 18, 6304.
-
(2016)
Org. Lett.
, vol.18
, pp. 6304
-
-
Zhao, Y.1
Chen, J.R.2
Xiao, W.J.3
-
19
-
-
85020556765
-
-
For selected reviews on the synthesis of tetrahydroquinolines, s
-
For selected reviews on the synthesis of tetrahydroquinolines, see:
-
-
-
-
20
-
-
0030602266
-
-
A. R. Katritzky, S. Rachwal, B. Rachwal, Tetrahedron 1996, 52, 15031;
-
(1996)
Tetrahedron
, vol.52
, pp. 15031
-
-
Katritzky, A.R.1
Rachwal, S.2
Rachwal, B.3
-
23
-
-
84872695279
-
-
G. Masson, C. Lalli, M. Benohoud, G. Dagousset, Chem. Soc. Rev. 2013, 42, 902;
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 902
-
-
Masson, G.1
Lalli, C.2
Benohoud, M.3
Dagousset, G.4
-
25
-
-
0030817973
-
-
K. Okuro, H. Kai, H. Alper, Tetrahedron: Asymmetry 1997, 8, 2307;
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 2307
-
-
Okuro, K.1
Kai, H.2
Alper, H.3
-
27
-
-
84919363703
-
-
L. Zhang, Z. Qureshi, L. Sonaglia, M. Lautens, Angew. Chem. Int. Ed. 2014, 53, 13850;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 13850
-
-
Zhang, L.1
Qureshi, Z.2
Sonaglia, L.3
Lautens, M.4
-
28
-
-
85008941506
-
-
Angew. Chem. 2014, 126, 14070;
-
(2014)
Angew. Chem.
, vol.126
, pp. 14070
-
-
-
29
-
-
84905259527
-
-
A. Lee, A. Younai, C. K. Price, J. Izquierdo, R. K. Mishra, K. A. Scheidt, J. Am. Chem. Soc. 2014, 136, 10589.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 10589
-
-
Lee, A.1
Younai, A.2
Price, C.K.3
Izquierdo, J.4
Mishra, R.K.5
Scheidt, K.A.6
-
30
-
-
85020586545
-
-
For reviews on catalyzed propargylic substitution, s
-
For reviews on catalyzed propargylic substitution, see:
-
-
-
-
32
-
-
84960093918
-
-
Angew. Chem. 2009, 121, 652;
-
(2009)
Angew. Chem.
, vol.121
, pp. 652
-
-
-
34
-
-
77952340938
-
-
Y. Miyake, S. Uemura, Y. Nishibayashi, ChemCatChem 2009, 1, 342;
-
(2009)
ChemCatChem
, vol.1
, pp. 342
-
-
Miyake, Y.1
Uemura, S.2
Nishibayashi, Y.3
-
38
-
-
84949115770
-
-
X.-H. Hu, Z.-T. Liu, H. Shao, X.-P. Hu, Synthesis 2015, 913;
-
(2015)
Synthesis
, pp. 913
-
-
Hu, X.-H.1
Liu, Z.-T.2
Shao, H.3
Hu, X.-P.4
-
40
-
-
0037055054
-
-
Y. Nishibayashi, Y. Inada, M. Hidai, S. Uemura, J. Am. Chem. Soc. 2002, 124, 7900;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 7900
-
-
Nishibayashi, Y.1
Inada, Y.2
Hidai, M.3
Uemura, S.4
-
41
-
-
2442701969
-
-
Y. Nishibayashi, M. Yoshikawa, Y. Inada, M. Hidai, S. Uemura, J. Org. Chem. 2004, 69, 3408;
-
(2004)
J. Org. Chem.
, vol.69
, pp. 3408
-
-
Nishibayashi, Y.1
Yoshikawa, M.2
Inada, Y.3
Hidai, M.4
Uemura, S.5
-
42
-
-
77951853107
-
-
K. Kanao, Y. Miyake, Y. Nishibayashi, Organometallics 2010, 29, 2126;
-
(2010)
Organometallics
, vol.29
, pp. 2126
-
-
Kanao, K.1
Miyake, Y.2
Nishibayashi, Y.3
-
43
-
-
84862224599
-
-
C. Zhang, X.-H. Hu, Y.-H. Wang, Z. Zheng, J. Xu, X.-P. Hu, J. Am. Chem. Soc. 2012, 134, 9585;
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 9585
-
-
Zhang, C.1
Hu, X.-H.2
Wang, Y.-H.3
Zheng, Z.4
Xu, J.5
Hu, X.-P.6
-
44
-
-
84908064850
-
-
F.-L. Zhu, Y.-H. Wang, D.-Y. Zhang, J. Xu, X.-P. Hu, Angew. Chem. Int. Ed. 2014, 53, 10223;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 10223
-
-
Zhu, F.-L.1
Wang, Y.-H.2
Zhang, D.-Y.3
Xu, J.4
Hu, X.-P.5
-
45
-
-
84926618910
-
-
Angew. Chem. 2014, 126, 10387;
-
(2014)
Angew. Chem.
, vol.126
, pp. 10387
-
-
-
46
-
-
77952324547
-
-
G. Hattori, Y. Miyake, Y. Nishibayashi, ChemCatChem 2010, 2, 155;
-
(2010)
ChemCatChem
, vol.2
, pp. 155
-
-
Hattori, G.1
Miyake, Y.2
Nishibayashi, Y.3
-
47
-
-
84935869255
-
-
W. Shao, H. Li, C. Liu, C. J. Liu, S. L. You, Angew. Chem. Int. Ed. 2015, 54, 7684;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 7684
-
-
Shao, W.1
Li, H.2
Liu, C.3
Liu, C.J.4
You, S.L.5
-
48
-
-
84977928714
-
-
Angew. Chem. 2015, 127, 7794;
-
(2015)
Angew. Chem.
, vol.127
, pp. 7794
-
-
-
49
-
-
84978792945
-
-
Q. Wang, T. R. Li, L. Q. Lu, M. M. Li, K. Zhang, W. J. Xiao, J. Am. Chem. Soc. 2016, 138, 8360;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 8360
-
-
Wang, Q.1
Li, T.R.2
Lu, L.Q.3
Li, M.M.4
Zhang, K.5
Xiao, W.J.6
-
50
-
-
84990218787
-
-
T. R. Li, B. Y. Cheng, Y. N. Wang, M. M. Zhang, L. Q. Lu, W. J. Xiao, Angew. Chem. Int. Ed. 2016, 55, 12422;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 12422
-
-
Li, T.R.1
Cheng, B.Y.2
Wang, Y.N.3
Zhang, M.M.4
Lu, L.Q.5
Xiao, W.J.6
-
51
-
-
85020109852
-
-
Angew. Chem. 2016, 128, 12610.
-
(2016)
Angew. Chem.
, vol.128
, pp. 12610
-
-
-
52
-
-
85020569687
-
-
For selected reviews, s
-
For selected reviews, see:
-
-
-
-
55
-
-
84906266327
-
-
D. F. Chen, Z. Y. Han, X. L. Zhou, L. Z. Gong, Acc. Chem. Res. 2014, 47, 2365;
-
(2014)
Acc. Chem. Res.
, vol.47
, pp. 2365
-
-
Chen, D.F.1
Han, Z.Y.2
Zhou, X.L.3
Gong, L.Z.4
-
59
-
-
6044270401
-
-
Angew. Chem. 2004, 116, 4666.
-
(2004)
Angew. Chem.
, vol.116
, pp. 4666
-
-
-
60
-
-
77956915666
-
-
M. Ikeda, Y. Miyake, Y. Nishibayashi, Angew. Chem. Int. Ed. 2010, 49, 7289;
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 7289
-
-
Ikeda, M.1
Miyake, Y.2
Nishibayashi, Y.3
-
61
-
-
79952046183
-
-
Angew. Chem. 2010, 122, 7447;
-
(2010)
Angew. Chem.
, vol.122
, pp. 7447
-
-
-
62
-
-
79951613334
-
-
A. Yoshida, M. Ikeda, G. Hattori, Y. Miyake, Y. Nishibayashi, Org. Lett. 2011, 13, 592.
-
(2011)
Org. Lett.
, vol.13
, pp. 592
-
-
Yoshida, A.1
Ikeda, M.2
Hattori, G.3
Miyake, Y.4
Nishibayashi, Y.5
-
63
-
-
84905280739
-
-
For a review on Lewis-base catalysis involving ammonium enolate reactivity, s
-
For a review on Lewis-base catalysis involving ammonium enolate reactivity, see: L. C. Morrill, A. D. Smith, Chem. Soc. Rev. 2014, 43, 6214.
-
(2014)
Chem. Soc. Rev.
, vol.43
, pp. 6214
-
-
Morrill, L.C.1
Smith, A.D.2
-
64
-
-
85020561667
-
-
For seminal and recent examples, s
-
For seminal and recent examples, see:
-
-
-
-
65
-
-
0034808095
-
-
G. S. Cortez, R. L. Tennyson, D. Romo, J. Am. Chem. Soc. 2001, 123, 7945;
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7945
-
-
Cortez, G.S.1
Tennyson, R.L.2
Romo, D.3
-
67
-
-
49449093005
-
-
V. C. Purohit, A. S. Malta, D. Romo, J. Am. Chem. Soc. 2008, 130, 10478;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 10478
-
-
Purohit, V.C.1
Malta, A.S.2
Romo, D.3
-
68
-
-
78650078134
-
-
C. A. Leverett, V. C. Purohit, D. Romo, Angew. Chem. Int. Ed. 2010, 49, 9479;
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 9479
-
-
Leverett, C.A.1
Purohit, V.C.2
Romo, D.3
-
69
-
-
84925127612
-
-
Angew. Chem. 2010, 122, 9669;
-
(2010)
Angew. Chem.
, vol.122
, pp. 9669
-
-
-
70
-
-
84894589142
-
-
S. R. Smith, J. Douglas, H. Prevet, P. Shapland, A. M. Z. Slawin, A. D. Smith, J. Org. Chem. 2014, 79, 1626;
-
(2014)
J. Org. Chem.
, vol.79
, pp. 1626
-
-
Smith, S.R.1
Douglas, J.2
Prevet, H.3
Shapland, P.4
Slawin, A.M.Z.5
Smith, A.D.6
-
71
-
-
84992504728
-
-
C. M. Young, D. G. Stark, T. H. West, J. E. Taylor, A. D. Smith, Angew. Chem. Int. Ed. 2016, 55, 14394;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 14394
-
-
Young, C.M.1
Stark, D.G.2
West, T.H.3
Taylor, J.E.4
Smith, A.D.5
-
72
-
-
85020561568
-
-
Angew. Chem. 2016, 128, 14606;
-
(2016)
Angew. Chem.
, vol.128
, pp. 14606
-
-
-
73
-
-
84966340531
-
-
K. J. Schwarz, J. L. Amos, J. C. Klein, D. T. Do, T. N. Snaddon, J. Am. Chem. Soc. 2016, 138, 5214;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 5214
-
-
Schwarz, K.J.1
Amos, J.L.2
Klein, J.C.3
Do, D.T.4
Snaddon, T.N.5
-
74
-
-
85015807833
-
-
X. Y. Jiang, J. J. Beiger, J. F. Hartwig, J. Am. Chem. Soc. 2017, 139, 87.
-
(2017)
J. Am. Chem. Soc.
, vol.139
, pp. 87
-
-
Jiang, X.Y.1
Beiger, J.J.2
Hartwig, J.F.3
-
75
-
-
85017383969
-
-
During the preparation of our manuscript, Gong and co-workers reported a similar cascade reaction in which a combination of Cu(CH, CN), PF, i, Pr-Pybox and BTM was employed as catalyst, In our catalysis system the optimal combination of catalysts is different to that reported by Gong and co-workersa relatively larger substrate scope was evaluated in our studie
-
During the preparation of our manuscript, Gong and co-workers reported a similar cascade reaction in which a combination of Cu(CH3CN)4PF6/iPr-Pybox and BTM was employed as catalyst: J. Song, Z. J. Zhang, L. Z. Gong, Angew. Chem. Int. Ed. 2017, 56, 5212. In our catalysis system the optimal combination of catalysts is different to that reported by Gong and co-workers, and a relatively larger substrate scope was evaluated in our studies.
-
(2017)
Angew. Chem. Int. Ed.
, vol.56
, pp. 5212
-
-
Song, J.1
Zhang, Z.J.2
Gong, L.Z.3
-
76
-
-
85020595615
-
-
For initial efforts on establishing of the structures of propargylic alcohol, see the Supporting Informatio
-
For initial efforts on establishing of the structures of propargylic alcohol derivatives and enolate precursors suited for the study and details of conditions optimization, see the Supporting Information.
-
-
-
-
78
-
-
85020602085
-
-
contains the supplementary crystallographic data for this paper, Crystallographic Data Centr
-
CCDC 1541659 (3 ha) contains the supplementary crystallographic data for this paper. These data are provided free of charge by The Cambridge Crystallographic Data Centre.
-
-
-
-
79
-
-
84863624104
-
-
P. Liu, X. Yang, V. B. Birman, K. N. Houk, Org. Lett. 2012, 14, 3288;
-
(2012)
Org. Lett.
, vol.14
, pp. 3288
-
-
Liu, P.1
Yang, X.2
Birman, V.B.3
Houk, K.N.4
-
80
-
-
84880024313
-
-
D. Belmessieri, D. B. Cordes, A. M. Z. Slawin, A. D. Smith, Org. Lett. 2013, 15, 3472;
-
(2013)
Org. Lett.
, vol.15
, pp. 3472
-
-
Belmessieri, D.1
Cordes, D.B.2
Slawin, A.M.Z.3
Smith, A.D.4
-
81
-
-
84897081812
-
-
T. H. West, D. S. B. Daniels, A. M. Z. Slawin, A. D. Smith, J. Am. Chem. Soc. 2014, 136, 4476.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 4476
-
-
West, T.H.1
Daniels, D.S.B.2
Slawin, A.M.Z.3
Smith, A.D.4
-
82
-
-
85020595723
-
-
In, Cu–allenylidene complexes, either mono-Cu or di-Cu, [5] and [6] for examples), no solid evidence has been found to support the specific structure of Cu–allenylidene complexe
-
In Cu-catalyzed propargylic substitution reactions, Cu–allenylidene complexes, either mono-Cu or di-Cu, were frequently included as key intermediates in the catalytic cycle and to explain the chiral induction (see Ref. [5] and [6] for examples). However, no solid evidence has been found to support the specific structure of Cu–allenylidene complexes.
-
-
-
|