-
1
-
-
34248221211
-
-
For a recent review involving uses of derivatives of 1, see.
-
For a recent review involving uses of derivatives of 1, see:, Y.-Q. Liu, L. Yang, X. Tian, Curr. Bioact. Compd. 2007, 3, 37.
-
(2007)
Curr. Bioact. Compd.
, vol.3
, pp. 37
-
-
Liu, Y.-Q.1
Yang, L.2
Tian, X.3
-
3
-
-
34547733485
-
-
For a recent review highlighting synthetic strategies toward aryltetralin lignans, see:, For total syntheses of 1, see
-
For a recent review highlighting synthetic strategies toward aryltetralin lignans, see:, J. D. Sellars, P. G. Steel, Eur. J. Org. Chem. 2007, 3815; For total syntheses of 1, see
-
(2007)
Eur. J. Org. Chem.
, pp. 3815
-
-
Sellars, J.D.1
Steel, P.G.2
-
8
-
-
0023768503
-
-
R. C. Andrews, S. J. Teague, A. I. Meyers, J. Am. Chem. Soc. 1988, 110, 7854
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 7854
-
-
Andrews, R.C.1
Teague, S.J.2
Meyers, A.I.3
-
11
-
-
0025755543
-
-
R. Van Speybroeck, H. Guo, J. Van der Eycken, M. Vandewalle, Tetrahedron 1991, 47, 4675
-
(1991)
Tetrahedron
, vol.47
, pp. 4675
-
-
Van Speybroeck, R.1
Guo, H.2
Van Der Eycken, J.3
Vandewalle, M.4
-
15
-
-
0030199884
-
-
S. B. Hadimani, R. P. Tanpure, S. V. Bhat, Tetrahedron Lett. 1996, 37, 4791
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4791
-
-
Hadimani, S.B.1
Tanpure, R.P.2
Bhat, S.V.3
-
16
-
-
0033960568
-
-
D. B. Berkowitz, S. Choi, J.-H. Maeng, J. Org. Chem. 2000, 65, 847
-
(2000)
J. Org. Chem.
, vol.65
, pp. 847
-
-
Berkowitz, D.B.1
Choi, S.2
Maeng, J.-H.3
-
17
-
-
0141888982
-
-
A. J. Reynolds, A. J. Scott, C. I. Turner, M. S. Sherburn, J. Am. Chem. Soc. 2003, 125, 12108
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 12108
-
-
Reynolds, A.J.1
Scott, A.J.2
Turner, C.I.3
Sherburn, M.S.4
-
18
-
-
34147173768
-
-
Y. Wu, H. Zhang, Y. Zhao, J. Zhao, J. Chen, L. Li, Org. Lett. 2007, 9, 1199
-
(2007)
Org. Lett.
, vol.9
, pp. 1199
-
-
Wu, Y.1
Zhang, H.2
Zhao, Y.3
Zhao, J.4
Chen, J.5
Li, L.6
-
19
-
-
60849114785
-
-
Y. Wu, J. Zhao, J. Chen, C. Pan, L. Li, H. Zhang, Org. Lett. 2009, 11, 597
-
(2009)
Org. Lett.
, vol.11
, pp. 597
-
-
Wu, Y.1
Zhao, J.2
Chen, J.3
Pan, C.4
Li, L.5
Zhang, H.6
-
21
-
-
54749151723
-
-
For formal syntheses of 1, see
-
Angew. Chem. Int. Ed. 2008, 47, 7557; For formal syntheses of 1, see
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7557
-
-
-
22
-
-
0017773181
-
-
A. S. Kende, L. S. Liebeskind, J. E. Mills, P. S. Rutledge, D. P. Curran, J. Am. Chem. Soc. 1977, 99, 7082
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 7082
-
-
Kende, A.S.1
Liebeskind, L.S.2
Mills, J.E.3
Rutledge, P.S.4
Curran, D.P.5
-
25
-
-
0029991379
-
-
M. Medarde, A. C. Ramos, E. Caballero, J. L. Lõpez, R. Peláez-Lamamié de Clairac, A. S. San Feliciano, Tetrahedron Lett. 1996, 37, 2663
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 2663
-
-
Medarde, M.1
Ramos, A.C.2
Caballero, E.3
Lõpez, J.L.4
Peláez- Lamamié De Clairac, R.5
San Feliciano, A.S.6
-
27
-
-
2542466672
-
-
J. J. Kennedy-Smith, L. A. Young, F. D. Toste, Org. Lett. 2004, 6, 1325
-
(2004)
Org. Lett.
, vol.6
, pp. 1325
-
-
Kennedy-Smith, J.J.1
Young, L.A.2
Toste, F.D.3
-
28
-
-
84875934795
-
-
M. Takahashi, N. Suzuki, T. Ishikawa, J. Org. Chem. 2013, 78, 3250
-
(2013)
J. Org. Chem.
, vol.78
, pp. 3250
-
-
Takahashi, M.1
Suzuki, N.2
Ishikawa, T.3
-
29
-
-
37649009484
-
-
For the synthesis of 4-epi 1, see
-
F. Mingoia, M. Vitale, D. Madec, G. Prestat, G. Poli, Tetrahedron Lett. 2008, 49, 760; For the synthesis of 4-epi 1, see
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 760
-
-
Mingoia, F.1
Vitale, M.2
Madec, D.3
Prestat, G.4
Poli, G.5
-
31
-
-
0022496595
-
-
D. M. Vyas, P. M. Skonezny, T. A. Jenks, T. W. Doyle, Tetrahedron Lett. 1986, 27, 3099
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 3099
-
-
Vyas, D.M.1
Skonezny, P.M.2
Jenks, T.A.3
Doyle, T.W.4
-
32
-
-
18744373827
-
-
U. Engelhardt, A. Sarkar, T. Linker, Angew. Chem. 2003, 115, 2591
-
(2003)
Angew. Chem.
, vol.115
, pp. 2591
-
-
Engelhardt, U.1
Sarkar, A.2
Linker, T.3
-
34
-
-
79960676884
-
-
C.-C. Wu, T.-K. Li, L. Farh, L.-Y. Lin, T.-S. Lin, Y.-J. Yu, T.-J. Yen, C.-W. Chiang, N.-L. Chan, Science 2011, 333, 459.
-
(2011)
Science
, vol.333
, pp. 459
-
-
Wu, C.-C.1
Li, T.-K.2
Farh, L.3
Lin, L.-Y.4
Lin, T.-S.5
Yu, Y.-J.6
Yen, T.-J.7
Chiang, C.-W.8
Chan, N.-L.9
-
35
-
-
85055223076
-
-
For comprehensive structure-activity relationship studies involving 2, see:, CRC, Boca Raton, Chap.
-
For comprehensive structure-activity relationship studies involving 2, see:, G. M. Cragg, D. G. I. Kingston, D. Newman, Anticancer Agents from Natural Products, CRC, Boca Raton, 2012, Chap. 5.
-
(2012)
Anticancer Agents from Natural Products
-
-
Cragg, G.M.1
Kingston, D.G.I.2
Newman, D.3
-
36
-
-
25444458063
-
-
V. G. Zaitsev, D. Shabashov, O. Daugulis, J. Am. Chem. Soc. 2005, 127, 13154
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13154
-
-
Zaitsev, V.G.1
Shabashov, D.2
Daugulis, O.3
-
41
-
-
84885126549
-
-
E. T. Nadres, G. I. Franco Santos, D. Shabashov, O. Daugulis, J. Org. Chem. 2013, 78, 9689.
-
(2013)
J. Org. Chem.
, vol.78
, pp. 9689
-
-
Nadres, E.T.1
Franco Santos, G.I.2
Shabashov, D.3
Daugulis, O.4
-
42
-
-
84869456845
-
-
M. Wasa, K. S. L. Chan, X.-G. Zhang, J. He, M. Miura, J.-Q. Yu, J. Am. Chem. Soc. 2012, 134, 18570
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 18570
-
-
Wasa, M.1
Chan, K.S.L.2
Zhang, X.-G.3
He, J.4
Miura, M.5
Yu, J.-Q.6
-
43
-
-
67651233294
-
-
M. Wasa, K. M. Engle, J.-Q. Yu, J. Am. Chem. Soc. 2009, 131, 9886
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 9886
-
-
Wasa, M.1
Engle, K.M.2
Yu, J.-Q.3
-
44
-
-
84884840141
-
-
T. M. Figg, M. Wasa, J.-Q. Yu, D. G. Musaev, J. Am. Chem. Soc. 2013, 135, 14206
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 14206
-
-
Figg, T.M.1
Wasa, M.2
Yu, J.-Q.3
Musaev, D.G.4
-
45
-
-
84874860520
-
-
J. He, M. Wasa, K. S. L. Chan, J.-Q. Yu, J. Am. Chem. Soc. 2013, 135, 3387
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 3387
-
-
He, J.1
Wasa, M.2
Chan, K.S.L.3
Yu, J.-Q.4
-
46
-
-
83055161417
-
-
M. Wasa, K. M. Engle, D. W. Lin, E. J. Yoo, J.-Q. Yu, J. Am. Chem. Soc. 2011, 133, 19598
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 19598
-
-
Wasa, M.1
Engle, K.M.2
Lin, D.W.3
Yoo, E.J.4
Yu, J.-Q.5
-
47
-
-
77949801096
-
-
M. Wasa, K. M. Engle, J.-Q. Yu, J. Am. Chem. Soc. 2010, 132, 3680
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 3680
-
-
Wasa, M.1
Engle, K.M.2
Yu, J.-Q.3
-
48
-
-
33947644069
-
-
R. Giri, N. Maugel, J.-J. Li, D.-H. Wang, S. P. Breazzano, L. B. Saunders, J.-Q. Yu, J. Am. Chem. Soc. 2007, 129, 3510
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 3510
-
-
Giri, R.1
Maugel, N.2
Li, J.-J.3
Wang, D.-H.4
Breazzano, S.P.5
Saunders, L.B.6
Yu, J.-Q.7
-
49
-
-
44949242600
-
-
D.-H. Wang, M. Wasa, R. Giri, J.-Q. Yu, J. Am. Chem. Soc. 2008, 130, 7190.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7190
-
-
Wang, D.-H.1
Wasa, M.2
Giri, R.3
Yu, J.-Q.4
-
50
-
-
84882270894
-
-
S.-Y. Zhang, Q. Li, G. He, W. A. Nack, G. Chen, J. Am. Chem. Soc. 2013, 135, 12135
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 12135
-
-
Zhang, S.-Y.1
Li, Q.2
He, G.3
Nack, W.A.4
Chen, G.5
-
51
-
-
84873667624
-
-
S.-Y. Zhang, G. He, W. A. Nack, Y. Zhao, Q. Li, G. Chen, J. Am. Chem. Soc. 2013, 135, 2124
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 2124
-
-
Zhang, S.-Y.1
He, G.2
Nack, W.A.3
Zhao, Y.4
Li, Q.5
Chen, G.6
-
52
-
-
84860797573
-
-
S.-Y. Zhang, G. He, Y. Zhao, K. Wright, W. A. Nack, G. Chen, J. Am. Chem. Soc. 2012, 134, 7313
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 7313
-
-
Zhang, S.-Y.1
He, G.2
Zhao, Y.3
Wright, K.4
Nack, W.A.5
Chen, G.6
-
53
-
-
84862908390
-
-
G. He, Y. Zhao, S. Zhang, C. Lu, G. Chen, J. Am. Chem. Soc. 2012, 134, 3
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 3
-
-
He, G.1
Zhao, Y.2
Zhang, S.3
Lu, C.4
Chen, G.5
-
56
-
-
84890483819
-
-
G. He, S.-Y. Zhang, W. A. Nack, Q. Li, G. Chen, Angew. Chem. 2013, 125, 11330
-
(2013)
Angew. Chem.
, vol.125
, pp. 11330
-
-
He, G.1
Zhang, S.-Y.2
Nack, W.A.3
Li, Q.4
Chen, G.5
-
58
-
-
33746872900
-
-
B. V. S. Reddy, L. R. Reddy, E. J. Corey, Org. Lett. 2006, 8, 3391
-
(2006)
Org. Lett.
, vol.8
, pp. 3391
-
-
Reddy, B.V.S.1
Reddy, L.R.2
Corey, E.J.3
-
59
-
-
80051721509
-
-
Y. Ano, M. Tobisu, N. Chatani, J. Am. Chem. Soc. 2011, 133, 12984
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 12984
-
-
Ano, Y.1
Tobisu, M.2
Chatani, N.3
-
60
-
-
84886778961
-
-
X. Ye, Z. He, T. Ahmed, K. Weise, N. Akhmedov, J. L. Petersen, X. Shi, Chem. Sci. 2013, 4, 3712
-
(2013)
Chem. Sci.
, vol.4
, pp. 3712
-
-
Ye, X.1
He, Z.2
Ahmed, T.3
Weise, K.4
Akhmedov, N.5
Petersen, J.L.6
Shi, X.7
-
61
-
-
84883298886
-
-
K. Chen, F. Hu, S.-Q. Zhang, B.-F. Shi, Chem. Sci. 2013, 4, 3906
-
(2013)
Chem. Sci.
, vol.4
, pp. 3906
-
-
Chen, K.1
Hu, F.2
Zhang, S.-Q.3
Shi, B.-F.4
-
62
-
-
84885044834
-
-
F.-J. Chen, S. Zhao, F. Hu, K. Chen, Q. Zhang, S.-Q. Zhang, B.-F. Shi, Chem. Sci. 2013, 4, 4187
-
(2013)
Chem. Sci.
, vol.4
, pp. 4187
-
-
Chen, F.-J.1
Zhao, S.2
Hu, F.3
Chen, K.4
Zhang, Q.5
Zhang, S.-Q.6
Shi, B.-F.7
-
63
-
-
84896334920
-
-
Q. Zhang, K. Chen, W. Rao, Y. Zhang, F.-J. Chen, B.-F. Shi, Angew. Chem. 2013, 125, 13833
-
(2013)
Angew. Chem.
, vol.125
, pp. 13833
-
-
Zhang, Q.1
Chen, K.2
Rao, W.3
Zhang, Y.4
Chen, F.-J.5
Shi, B.-F.6
-
65
-
-
84896346652
-
-
G. Shan, X. Yang, Y. Zong, Y. Rao, Angew. Chem. 2013, 125, 1
-
(2013)
Angew. Chem.
, vol.125
, pp. 1
-
-
Shan, G.1
Yang, X.2
Zong, Y.3
Rao, Y.4
-
66
-
-
84896322317
-
-
For a related iron-catalyzed method, see
-
Angew. Chem. Int. Ed. 2013, 52, 1 For a related iron-catalyzed method, see
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 1
-
-
-
67
-
-
84876711631
-
-
R. Shang, L. Ilies, A. Matsumoto, E. Nakamura, J. Am. Chem. Soc. 2013, 135, 6030.
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 6030
-
-
Shang, R.1
Ilies, L.2
Matsumoto, A.3
Nakamura, E.4
-
71
-
-
84867044853
-
-
W. R. Gutekunst, R. Gianatassio, P. S. Baran, Angew. Chem. 2012, 124, 7625
-
(2012)
Angew. Chem.
, vol.124
, pp. 7625
-
-
Gutekunst, W.R.1
Gianatassio, R.2
Baran, P.S.3
-
75
-
-
0001253325
-
-
E. Akgün, E. M. B. Glinski, K. L. Dhawan, T. Durst, J. Org. Chem. 1981, 46, 2730.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 2730
-
-
Akgün, E.1
Glinski, E.M.B.2
Dhawan, K.L.3
Durst, T.4
-
76
-
-
54849436434
-
-
For two-step β-lactam synthesis through based on Ci-H functionalization (i.e. Ci-H halogenation/cyclization, see.
-
For two-step β-lactam synthesis through based on Ci-H functionalization (i.e. Ci-H halogenation/cyclization, see:, M. Wasa, J.-Q. Yu, J. Am. Chem. Soc. 2008, 130, 14058-14059.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 14058-14059
-
-
Wasa, M.1
Yu, J.-Q.2
-
77
-
-
84896330102
-
-
articles ASAP
-
3)-H activation processes, the β-lactam-forming pathway can become favorable over the arylation pathway, see: W.-W. Sun, P. Cao, R.-Q. Mei, Y. Li, Y.-L. Ma, B. Wu, Org. Lett. 2013, articles ASAP, DOI:.
-
(2013)
Org. Lett.
-
-
Sun, W.-W.1
Cao, P.2
Mei, R.-Q.3
Li, Y.4
Ma, Y.-L.5
Wu, B.6
-
78
-
-
0002521519
-
-
IV center typically precedes Ci-C reductive elimination, see.
-
IV center typically precedes Ci-C reductive elimination, see:, A. J. Canty, Acc. Chem. Res. 1992, 25, 83.
-
(1992)
Acc. Chem. Res.
, vol.25
, pp. 83
-
-
Canty, A.J.1
-
80
-
-
79960914042
-
-
For a discussion on this topic, see
-
For a discussion on this topic, see:, K. M. Engle, T.-S. Mei, X. Wang, J.-Q. Yu, Angew. Chem. 2011, 123, 1514
-
(2011)
Angew. Chem.
, vol.123
, pp. 1514
-
-
Engle, K.M.1
Mei, T.-S.2
Wang, X.3
Yu, J.-Q.4
|