-
1
-
-
0001615883
-
-
Wilzbach, K. E.; Harkness, A. L.; Kaplan, L. J. Am. Chem. Soc. 1968, 90, 1116.
-
(1968)
J. Am. Chem. Soc
, vol.90
, pp. 1116
-
-
Wilzbach, K.E.1
Harkness, A.L.2
Kaplan, L.3
-
3
-
-
33947085056
-
-
(b) Chapman, O. L.; McIntosh, C. L.; Pacansky, J. J. Am. Chem. Soc. 1973, 95, 614.
-
(1973)
J. Am. Chem. Soc
, vol.95
, pp. 614
-
-
Chapman, O.L.1
McIntosh, C.L.2
Pacansky, J.3
-
5
-
-
0141811897
-
-
Cundall, R. B.; Fletcher, F. J.; Milne, D. G. Trans. Faraday Soc. 1964, 60, 1146.
-
(1964)
Trans. Faraday Soc
, vol.60
, pp. 1146
-
-
Cundall, R.B.1
Fletcher, F.J.2
Milne, D.G.3
-
7
-
-
41649087433
-
-
Irradiation at 193, 213.9, or 228.8 nm has been reported to result in ring cleavage. See: (a) Mathias, E.; Heicklen, J. Mol. Photochem. 1972, 4, 483.
-
Irradiation at 193, 213.9, or 228.8 nm has been reported to result in ring cleavage. See: (a) Mathias, E.; Heicklen, J. Mol. Photochem. 1972, 4, 483.
-
-
-
-
8
-
-
23944522638
-
-
(b) Lin, M.-F.; Dyakov, Y. A.; Tseng, C.-M.; Mebel, A. M.; Lin, S. H.; Lee, Y. T.; Ni, C.-K. J. Chem. Phys. 2005, 123, 054309.
-
(2005)
J. Chem. Phys
, vol.123
, pp. 054309
-
-
Lin, M.-F.1
Dyakov, Y.A.2
Tseng, C.-M.3
Mebel, A.M.4
Lin, S.H.5
Lee, Y.T.6
Ni, C.-K.7
-
9
-
-
0033597604
-
-
Pavlik, J. W.; Kebede, N.; Thompson, M.; Day, A. C.; Barltrop, J. A. J. Am. Chem. Soc. 1999, 121, 5666.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 5666
-
-
Pavlik, J.W.1
Kebede, N.2
Thompson, M.3
Day, A.C.4
Barltrop, J.A.5
-
10
-
-
34548718691
-
-
Pavlik, J. W.; Laohhasurayotin, S.; Vongnakorn, T. J. Org. Chem. 2007, 72, 7116.
-
(2007)
J. Org. Chem
, vol.72
, pp. 7116
-
-
Pavlik, J.W.1
Laohhasurayotin, S.2
Vongnakorn, T.3
-
11
-
-
37049120561
-
-
A similar biradical structure called prefulvene was first suggested to be an intermediate in the photoisomerization of benzene. See: Bryce-Smith, D, Longuet-Higgins, H. C. J. Chem. Soc, Chem. Commun. 1966, 17, 593
-
A similar biradical structure called prefulvene was first suggested to be an intermediate in the photoisomerization of benzene. See: Bryce-Smith, D.; Longuet-Higgins, H. C. J. Chem. Soc., Chem. Commun. 1966, 17, 593.
-
-
-
-
13
-
-
0001018235
-
-
Sobolewski, A. L.; Woywod, C.; Domke, W. J. Chem. Phys. 1993, 98, 5627.
-
(1993)
J. Chem. Phys
, vol.98
, pp. 5627
-
-
Sobolewski, A.L.1
Woywod, C.2
Domke, W.3
-
14
-
-
0000871650
-
-
Zhang, D.; Dian, E. W.-G.; Bernhardt, T.; De Feyter, S.; Roberts, J. D.; Zewail, A. H. Chem. Phys. Lett. 1998, 298, 129.
-
(1998)
Chem. Phys. Lett
, vol.298
, pp. 129
-
-
Zhang, D.1
Dian, E.W.-G.2
Bernhardt, T.3
De Feyter, S.4
Roberts, J.D.5
Zewail, A.H.6
-
15
-
-
0035805239
-
-
Cao, Z.; Zhang, Q.; Peyerimhoff, S. D. Chem. - Eur. J. 2001, 7, 1927.
-
(2001)
Chem. - Eur. J
, vol.7
, pp. 1927
-
-
Cao, Z.1
Zhang, Q.2
Peyerimhoff, S.D.3
-
20
-
-
41649086193
-
-
In the present study, since product mixtures could not be analyzed by glpc, small amounts of leakage products would be difficult to detect
-
In the present study, since product mixtures could not be analyzed by glpc, small amounts of leakage products would be difficult to detect.
-
-
-
-
21
-
-
37049138104
-
-
Pyridine phototranspositions were originally suggested to occur via Dewar pyridine intermediates. See: Caplain, S, Lablache-Combier, A. J. Chem. Soc, Chem. Commun. 1969, 1247. Subsequent work showed that Dewar pyridines are only minor intermediates in these reactions. See ref 7
-
Pyridine phototranspositions were originally suggested to occur via Dewar pyridine intermediates. See: Caplain, S.; Lablache-Combier, A. J. Chem. Soc., Chem. Commun. 1969, 1247. Subsequent work showed that Dewar pyridines are only minor intermediates in these reactions. See ref 7.
-
-
-
|