-
8
-
-
0036291384
-
Lectures presented at the 11th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS-11), Taipei, Taiwan, 22-26 July 2001
-
(b) Tien-Yau Luh, Lectures presented at the 11th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS-11), Taipei, Taiwan, 22-26 July 2001, Pure Appl. Chem., 2002, 74, 1, 1-186;
-
(2002)
Pure Appl. Chem.
, vol.74
, Issue.1
, pp. 1-186
-
-
Luh, T.-Y.1
-
10
-
-
0026418434
-
-
(a) B. M. Trost, Science, 1991, 254, 1471;
-
(1991)
Science
, vol.254
, pp. 1471
-
-
Trost, B.M.1
-
13
-
-
3142763237
-
-
T. Shibata, T. Fujimoto, K. Yokota and K. Takagi, J. Am. Chem. Soc., 2004, 126, 8382.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8382
-
-
Shibata, T.1
Fujimoto, T.2
Yokota, K.3
Takagi, K.4
-
14
-
-
0001136410
-
-
ed. L. S. Hegedus, Pergamon Press, Oxford
-
(a) N. E. Schore, in Comprehensive Organometallic Chemistry II, ed. L. S. Hegedus, Pergamon Press, Oxford, 1999, vol. 12, pp. 703-739;
-
(1999)
Comprehensive Organometallic Chemistry II
, vol.12
, pp. 703-739
-
-
Schore, N.E.1
-
15
-
-
0002110351
-
-
(b) M. Lautens, W. Klute and W. Tam, Chem. Rev., 1996, 96, 49;
-
(1996)
Chem. Rev.
, vol.96
, pp. 49
-
-
Lautens, M.1
Klute, W.2
Tam, W.3
-
17
-
-
33845278920
-
-
(a) T. Hayashi, K. Hayashizaki, T. Kiyoi and Y. Ito, J. Am. Chem. Soc., 1988, 110, 8153;
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 8153
-
-
Hayashi, T.1
Hayashizaki, K.2
Kiyoi, T.3
Ito, Y.4
-
18
-
-
0001578739
-
-
(b) T. Hayashi, S. Niizuma, T. Kamikawa, N. Suzuki and Y. Uozumi, J. Am. Chem. Soc., 1995, 117, 9101;
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 9101
-
-
Hayashi, T.1
Niizuma, S.2
Kamikawa, T.3
Suzuki, N.4
Uozumi, Y.5
-
19
-
-
0029592611
-
-
(c) M. Nakajima, K. Kanayama, I. Miyoshi and S.-I. Hashimoto, Tetrahedron Lett., 1995, 36, 9519;
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 9519
-
-
Nakajima, M.1
Kanayama, K.2
Miyoshi, I.3
Hashimoto, S.-I.4
-
20
-
-
0033615324
-
-
(d) S. Saito, T. Kano, H. Muto, M. Nakadai and H. Yamamoto, J. Am. Chem. Soc., 1999, 121, 8943;
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 8943
-
-
Saito, S.1
Kano, T.2
Muto, H.3
Nakadai, M.4
Yamamoto, H.5
-
23
-
-
0035822065
-
-
(g) C.-Y. Chu, D.-R. Hwang, S.-K. Wang and B.-J. Uang, Chem. Commun., 2001, 980;
-
(2001)
Chem. Commun.
, pp. 980
-
-
Chu, C.-Y.1
Hwang, D.-R.2
Wang, S.-K.3
Uang, B.-J.4
-
24
-
-
0038676302
-
-
(h) X. Li, J. B. Hewgley, C. A. Mulrooney, J. Yang and M. C. Kozlowski, J. Org. Chem., 2003, 68, 5500.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 5500
-
-
Li, X.1
Hewgley, J.B.2
Mulrooney, C.A.3
Yang, J.4
Kozlowski, M.C.5
-
25
-
-
24644462889
-
-
A recent review of the synthesis of atropoisomeric biaryl skeletons with axial chirality: G. Bringmann, A. J. P. Mortimer, P. A. Keller, M. J. Gresser, J. Garner and M. Breuning, Angew. Chem., Int. Ed., 2005, 44, 5384.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 5384
-
-
Bringmann, G.1
Mortimer, A.J.P.2
Keller, P.A.3
Gresser, M.J.4
Garner, J.5
Breuning, M.6
-
26
-
-
0033525671
-
-
The pioneering work on the enantioselective [2 + 2 + 2] cycloaddition of triynes for the synthesis of helicene derivatives: I. G. Stará, I. Stary, A. Kollárovic, F. Teply, S. Vyskocil and D. Saman, Tetrahedron Lett., 1999, 40, 1993.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 1993
-
-
Stará, I.G.1
Stary, I.2
Kollárovic, A.3
Teply, F.4
Vyskocil, S.5
Saman, D.6
-
27
-
-
4544286694
-
-
Other than us, two groups independently reported cobalt and rhodium complex-catalyzed [2 + 2 + 2] cycloadditions for the synthesis of an atropoisomeric biaryl with an axial chirality. They used diynes with no substituent on one of two alkyne termini: (a) A. Gutnov, B. Heller, C. Fischer, H.-J. Drexler, A. Spannenberg, B. Sundermann and C. Sundermann, Angew. Chem., Int. Ed., 2004, 43, 3795;
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 3795
-
-
Gutnov, A.1
Heller, B.2
Fischer, C.3
Drexler, H.-J.4
Spannenberg, A.5
Sundermann, B.6
Sundermann, C.7
-
28
-
-
11144315960
-
-
(b) K. Tanaka, G. Nishida, A. Wada and K. Noguchi, Angew. Chem., Int. Ed., 2004, 43, 6510.
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 6510
-
-
Tanaka, K.1
Nishida, G.2
Wada, A.3
Noguchi, K.4
-
29
-
-
29744447757
-
-
note
-
Ee was determined by high-performance liquid chromatography (HPLC) using a chiral stationary phase column (see supporting informationt). A >99% ee means that the minor enantiomer could not be detected.
-
-
-
-
30
-
-
29744457752
-
-
note
-
In each reaction, diastereomers could not be detected during the purification of the products using thin layer chromatography on silica gel or by NMR measurement of cycloadducts 2.
-
-
-
-
31
-
-
22944431902
-
-
Teraryl compounds were used as a synthetic scaffold that mimics an α-helix, the key element of a protein surface in biochemical research: H. Yin, G. Lee, K. A. Sedey, O. Kutzki, H. S. Park, B. P. Orner, J. T. Ernst, H.-G. Wang, S. M. Sebti and A. D. Hamilton, J. Am. Chem. Soc., 2005, 127, 10191.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10191
-
-
Yin, H.1
Lee, G.2
Sedey, K.A.3
Kutzki, O.4
Park, H.S.5
Orner, B.P.6
Ernst, J.T.7
Wang, H.-G.8
Sebti, S.M.9
Hamilton, A.D.10
|