-
4
-
-
67650059255
-
-
ed. J. Siegel and Y. Tobe, Thieme, Stuttgart, 483-506
-
H. Sano and J. Nishimura, Science of Synthesis, ed., J. Siegel, and, Y. Tobe, Thieme, Stuttgart, 2009, vol. 45a, pp. 483-506
-
(2009)
Science of Synthesis
, vol.45
-
-
Sano, H.1
Nishimura, J.2
-
15
-
-
84871556696
-
-
T. Suzuki Y. Sakano T. Iwai S. Iwashita Y. Miura R. Katoono H. Kawai K. Fujiwara Y. Tsuji T. Fukushima Chem.-Eur. J. 2013 19 117 123
-
(2013)
Chem.-Eur. J.
, vol.19
, pp. 117-123
-
-
Suzuki, T.1
Sakano, Y.2
Iwai, T.3
Iwashita, S.4
Miura, Y.5
Katoono, R.6
Kawai, H.7
Fujiwara, K.8
Tsuji, Y.9
Fukushima, T.10
-
18
-
-
24444480839
-
-
W. P. Cofino M. Engelsma D. A. Kamminga G. Ph. Hoornweg C. Gooijer C. MacLean N. H. Velthost Spectrochim. Acta, Part A 1984 40 269 273
-
(1984)
Spectrochim. Acta, Part A
, vol.40
, pp. 269-273
-
-
Cofino, W.P.1
Engelsma, M.2
Kamminga, D.A.3
Hoornweg, G.Ph.4
Gooijer, C.5
MacLean, C.6
Velthost, N.H.7
-
24
-
-
27144481377
-
-
T. Kubo A. Shimizu M. Sakamoto M. Uruichi K. Yakushi M. Nakano D. Shiomi K. Sato T. Takui Y. Morita K. Nakasuji Angew. Chem., Int. Ed. 2005 44 6564 6568
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 6564-6568
-
-
Kubo, T.1
Shimizu, A.2
Sakamoto, M.3
Uruichi, M.4
Yakushi, K.5
Nakano, M.6
Shiomi, D.7
Sato, K.8
Takui, T.9
Morita, Y.10
Nakasuji, K.11
-
25
-
-
33846435318
-
-
T. Kubo A. Shimizu M. Uruichi K. Yakushi M. Nakano D. Shiomi K. Sato T. Takui Y. Morita K. Nakasuji Org. Lett. 2007 9 81 84
-
(2007)
Org. Lett.
, vol.9
, pp. 81-84
-
-
Kubo, T.1
Shimizu, A.2
Uruichi, M.3
Yakushi, K.4
Nakano, M.5
Shiomi, D.6
Sato, K.7
Takui, T.8
Morita, Y.9
Nakasuji, K.10
-
28
-
-
84865801594
-
-
Y. Li W.-K. Heng B. S. Lee N. Aratani J. L. Zafra N. Bao R. Lee Y. M. Sung Z. Sun K.-W. Huang R. D. Webster J. T. L. Navarrete D. Kim A. Osuka J. Casado J. Ding J. Wu J. Am. Chem. Soc. 2012 134 14913 14922
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 14913-14922
-
-
Li, Y.1
Heng, W.-K.2
Lee, B.S.3
Aratani, N.4
Zafra, J.L.5
Bao, N.6
Lee, R.7
Sung, Y.M.8
Sun, Z.9
Huang, K.-W.10
Webster, R.D.11
Navarrete, J.T.L.12
Kim, D.13
Osuka, A.14
Casado, J.15
Ding, J.16
Wu, J.17
-
29
-
-
77955587750
-
-
A. Konishi Y. Hirao M. Nakano A. Shimizu E. Botek B. Champagne D. Shiomi K. Sato T. Takui K. Matsumoto H. Kurata T. Kubo J. Am. Chem. Soc. 2010 132 11021 11023
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 11021-11023
-
-
Konishi, A.1
Hirao, Y.2
Nakano, M.3
Shimizu, A.4
Botek, E.5
Champagne, B.6
Shiomi, D.7
Sato, K.8
Takui, T.9
Matsumoto, K.10
Kurata, H.11
Kubo, T.12
-
30
-
-
84873862930
-
-
A. Konishi Y. Hirao K. Matsumoto H. Kurata R. Kishi Y. Shigeta M. Nakano K. Tokunaga K. Kamada T. Kubo J. Am. Chem. Soc. 2013 135 1430 1437
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 1430-1437
-
-
Konishi, A.1
Hirao, Y.2
Matsumoto, K.3
Kurata, H.4
Kishi, R.5
Shigeta, Y.6
Nakano, M.7
Tokunaga, K.8
Kamada, K.9
Kubo, T.10
-
33
-
-
84863448195
-
-
D. T. Chase A. G. Fix S. J. Kang B. D. Rose C. D. Weber Y. Zhong L. N. Zakharov M. C. Lonergan C. Nuckolls M. M. Haley J. Am. Chem. Soc. 2012 134 10349 10352
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 10349-10352
-
-
Chase, D.T.1
Fix, A.G.2
Kang, S.J.3
Rose, B.D.4
Weber, C.D.5
Zhong, Y.6
Zakharov, L.N.7
Lonergan, M.C.8
Nuckolls, C.9
Haley, M.M.10
-
37
-
-
84934908949
-
-
10.1007/128-2012-376. Recently, Haley and co-workers added a new member of p-QDM, indeno[2,1-c]fluorene, to the indenofluorene family
-
A. G. Fix D. T. Chase M. M. Haley Top. Curr. Chem. 10.1007/128-2012-376
-
Top. Curr. Chem.
-
-
Fix, A.G.1
Chase, D.T.2
Haley, M.M.3
-
38
-
-
84875197286
-
-
We also reported indeno[2,1-b]fluorene, a meta-quinodimethane congener
-
A. G. Fix P. E. Deal C. L. Vonnegut B. D. Rose L. N. Zakharov M. M. Haley Org. Lett. 2013 15 1362 1365
-
(2013)
Org. Lett.
, vol.15
, pp. 1362-1365
-
-
Fix, A.G.1
Deal, P.E.2
Vonnegut, C.L.3
Rose, B.D.4
Zakharov, L.N.5
Haley, M.M.6
-
39
-
-
84878405379
-
-
A. Shimizu R. Kishi M. Nakano D. Shiomi K. Sato T. Takui I. Hisaki M. Miyata Y. Tobe Angew. Chem., Int. Ed. 2013 52 6076 6079
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 6076-6079
-
-
Shimizu, A.1
Kishi, R.2
Nakano, M.3
Shiomi, D.4
Sato, K.5
Takui, T.6
Hisaki, I.7
Miyata, M.8
Tobe, Y.9
-
40
-
-
33947435033
-
-
Though diol 11 was obtained as a single isomer, its stereochemistry was not determined It should be pointed out that for 11,12-diphenylindeno[2,1-a] fluorene (8c), Le Berre reported that oxygen added to the exo-methylene carbons yielding the corresponding cyclic peroxide which further degradated to give bond cleaved products. 12a Similarly, attempts to prepare NQD derivative 9c resulted in the formation of decomposition products derived from oxygenation at the exo-methylene carbons 12a
-
C. F. Koelsch H. J. Richter J. Org. Chem. 1938 3 465 472
-
(1938)
J. Org. Chem.
, vol.3
, pp. 465-472
-
-
Koelsch, C.F.1
Richter, H.J.2
-
45
-
-
0037130668
-
-
Y. Takano T. Taniguchi H. Isobe T. Kubo Y. Morita K. Yamamoto K. Nakasuji T. Takui K. Yamaguchi J. Am. Chem. Soc. 2002 124 11122 11130
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 11122-11130
-
-
Takano, Y.1
Taniguchi, T.2
Isobe, H.3
Kubo, T.4
Morita, Y.5
Yamamoto, K.6
Nakasuji, K.7
Takui, T.8
Yamaguchi, K.9
-
57
-
-
0001033243
-
-
Le Berre reported that maleic anhydride added to the exo-methylene carbons of 11,12-diphenylindeno[2,1-a]fluorene (8c), though the structure was not concretely established. 12a Similarly, an attempt to prepare NQD derivative 9c in the presence of maleic anhydride gave an adduct at the exo-methylene carbons. 12a On the other hand, we reported that dimesityl derivative 8b did not react with maleic anhydride when a toluene solution of them was heated at 100 °C, 12b showing the efficient protecting effect of the mesityl groups
-
K. K. Baldridge J. S. Siegel J. Am. Chem. Soc. 1992 114 9583 9587
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9583-9587
-
-
Baldridge, K.K.1
Siegel, J.S.2
|