References
[1]
(a) H. Tong, Y. Dong, M. Häußler, J. W. Y. Lam, H. H. Y. Sung, I. D. Williams, J. Sun, B. Z. Tang,
Chem. Commun. 2006, 1133.
|
CrossRef |
(b) H. Tong, Y. Dong, Y. Hong, M. Haussier, J. W. Y. Lam, H. H. Y. Sung, X. Yu, J. Sun, I. D. Williams, H. S. Kwok, B. Z. Tang,
J. Phys. Chem. C 2007,
111, 2287.
|
CrossRef |
(c) X. Luo, J. Li, C. Li, L. Heng, Y. Q. Dong, Z. Liu, Z. Bo, B. Z. Tang,
Adv. Mater. 2011,
23, 3261.
|
CrossRef |
(d) F. G. Brunetti, X. Gong, M. Tong, A. J. Heeger, F. Wudl,
Angew. Chem. Int. Ed. 2010,
49, 532.
|
CrossRef |
(e) F. G. Brunetti, A. Varotto, N. A. Batara, F. Wudl,
Chem.–Eur. J. 2011,
17, 8604.
|
CrossRef |
(f) H. Usta, A. Facchetti, T. J. Marks,
J. Am. Chem. Soc. 2008,
130, 8580.
|
CrossRef |
(g) H. Usta, A. Facchetti, T. J. Marks,
Org. Lett. 2008,
10, 1385.
|
CrossRef |
(h) H. Usta, C. Risko, Z. Wang, H. Huang, M. K. Deliomeroglu, A. Zhukhovitskiy, A. Facchetti, T. J. Marks,
J. Am. Chem. Soc. 2009,
131, 5586.
|
CrossRef |
(i) J. Vicario, M. Walko, A. Meetsma, B. L. Feringa,
J. Am. Chem. Soc. 2006,
128, 5127.
|
CrossRef |
(j) R. Eelkema, B. L. Feringa,
Chem. Asian J. 2006,
1, 367.
|
CrossRef |
(k) D. Pijper, B. L. Feringa,
Angew. Chem. Int. Ed. 2007,
46, 3693.
|
CrossRef |
(l) T. L. Andrew, J. R. Cox, T. M. Swager,
Org. Lett. 2010,
12, 5302.
|
CrossRef |
[2]
M. L. T. M. B. Franco, B. J. Herold, J. C. Evans, C. C. Rowlands,
J. Chem. Soc., Perkin Trans. 2 1988, 443.
|
CrossRef |
CAS |
[3]
M. Banerjee, S. J. Emond, S. V. Lindeman, R. Rathore,
J. Org. Chem. 2007,
72, 8054.
|
CrossRef |
CAS |
[4]
(a) N. Chernyak, V. Gevorgyan,
J. Am. Chem. Soc. 2008,
130, 5636.
|
CrossRef |
CAS |
(b) N. Chernyak, V. Gevorgyan,
Adv. Synth. Catal. 2009,
351, 1101.
|
CrossRef |
(c) S. A. Kandil, R. E. Dessy,
J. Am. Chem. Soc. 1966,
88, 3027.
See also
|
CrossRef |
[5]
(a) Q. Tian, R. C. Larock,
Org. Lett. 2000,
2, 3329.
|
CrossRef |
CAS |
(b) R. C. Larock, Q. Tian,
J. Org. Chem. 2001,
66, 7372.
|
CrossRef |
(c) T. Morishita, H. Yoshida, J. Ohshita,
Chem. Commun. 2010,
46, 640.
See also
|
CrossRef |
[6]
V. S. Thirunavukkarasu, K. Parthasarathy, C.-H. Cheng,
Chem.–Eur. J. 2010,
16, 1436.
|
CrossRef |
CAS |
[7]
(a) C. V. Ramana, B. K. Kishore Reddy, C. Nageswara Reddy, R. G. Gonnade, M. K. Gurjar,
Synlett 2007, 127.
|
CrossRef |
CAS |
(b) S. Paul, T. Gorai, A. Koley, J. K. Ray,
Tetrahedron Lett. 2011,
52, 4051.
|
CrossRef |
[8]
(a) M. Shimizu, I. Nagao, Y. Tomioka, T. Hiyama,
Angew. Chem. Int. Ed. 2008,
47, 8096.
|
CrossRef |
CAS |
(b) M. Shimizu, Y. Tomioka, I. Nagao, T. Hiyama,
Synlett 2009, 3147.
|
CrossRef |
(c) M. Shimizu, I. Nagao, Y. Tomioka, T. Kadowaki, T. Hiyama,
Tetrahedron 2011,
67, 8014.
|
CrossRef |
(d) I. Nagao, M. Shimizu, T. Hiyama,
Angew. Chem. Int. Ed. 2009,
48, 7573.
|
CrossRef |
[9]
(a) T. Hata, H. Kitagawa, H. Masai, T. Kurahashi, M. Shimizu, T. Hiyama,
Angew. Chem. Int. Ed. 2001,
40, 790.
|
CrossRef |
CAS |
(b) T. Kurahashi, T. Hata, H. Masai, H. Kitagawa, M. Shimizu, T. Hiyama,
Tetrahedron 2002,
58, 6381.
|
CrossRef |
(c) M. Shimizu, C. Nakamaki, K. Shimono, M. Schelper, T. Kurahashi, T. Hiyama,
J. Am. Chem. Soc. 2005,
127, 1250.
|
CrossRef |
[10]
In ref. [8d], two examples of the annulation using
7 and 1,1-dibromoalk-1-enes were preliminarily reported.
[11]
To the best of our knowledge, this is the first synthesis of dinaphthofulvenes of type
4e.