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1
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0001938751
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Kadish K.M., Smith K.M., and Guilard R. (Eds), The Academic Press, San Diego, CA
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Lindsay J.S. In: Kadish K.M., Smith K.M., and Guilard R. (Eds). The Porphyrin Handbook Vol. 1 (2000), The Academic Press, San Diego, CA 45-118
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Lindsay, J.S.1
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2
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33645459913
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Yamada H., Kushibe K., Okujima T., Uno H., and Ono N. Chem. Commun. (2006) 383-385
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Yamada, H.1
Kushibe, K.2
Okujima, T.3
Uno, H.4
Ono, N.5
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10
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0025899576
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Morgan A.R., Garbo G.M., Keck R.W., Selman S.H., and Skalkos D. J. Med. Chem. 34 (1991) 2126-2133
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Morgan, A.R.1
Garbo, G.M.2
Keck, R.W.3
Selman, S.H.4
Skalkos, D.5
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11
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0000599217
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Yeung M., Ng A.C.H., Drew M.G.B., Vorpagel E., Breitung E.M., McMahon R.J., and Ng D.K.P. J. Org. Chem. 63 (1998) 7143-7150
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Yeung, M.1
Ng, A.C.H.2
Drew, M.G.B.3
Vorpagel, E.4
Breitung, E.M.5
McMahon, R.J.6
Ng, D.K.P.7
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12
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0037423255
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2, but triphyrin was mainly prepared in the presence of trifluoroacetic acid.
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2, but triphyrin was mainly prepared in the presence of trifluoroacetic acid. Krivokapic A., Cowley A.R., Anderson H.L. J. Org. Chem. 68 (2003) 1089-1096
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Krivokapic, A.1
Cowley, A.R.2
Anderson, H.L.3
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13
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45549122294
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note
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We have already reported that the cis-type porphyrin was prepared at first and has changed to trans-type by room light during the work-up and column chromatography.The cis-type porphyrin can be also changed to trans-type by photo-irradiation, intendedly. See Ref. 2.
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14
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45649083138
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note
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Crystallographic data (excluding structure factors) for the structures in this Letter have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 684217. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: 144-(0)1223-336033 ore-mail: deposit@ccdc.cam.ac.uk].
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16
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29544437353
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A recent example of stabilization by silyl group is as follows. In this Letter, however, β-phenyl group also showed stabilizing effect similar to silyl groups in the hydroalumination reaction.
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A recent example of stabilization by silyl group is as follows. In this Letter, however, β-phenyl group also showed stabilizing effect similar to silyl groups in the hydroalumination reaction. Igawa K., and Tomooka K. Angew. Chem., Int. Ed. 45 (2006) 232-234
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Igawa, K.1
Tomooka, K.2
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17
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0001573613
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For the stabilization effect of tris(bicyclo[2.2.2]octeno)benzene, following literatures have been reported;
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For the stabilization effect of tris(bicyclo[2.2.2]octeno)benzene, following literatures have been reported;. Komatsu K., Akamatsu H., Jinbu Y., and Okamoto K. J. Am. Chem. Soc. 110 (1988) 633-634
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Komatsu, K.1
Akamatsu, H.2
Jinbu, Y.3
Okamoto, K.4
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18
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33751500307
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Komatsu K., Aonuma S., Jinbu Y., Tsuji R., Hirosawa C., and Takeuchi K.i. J. Org. Chem. 56 (1991) 195-203
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Komatsu, K.1
Aonuma, S.2
Jinbu, Y.3
Tsuji, R.4
Hirosawa, C.5
Takeuchi, K.i.6
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20
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0033972340
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Ito S., Ochi N., Murashima T., Uno H., and Ono N. Heterocycles 52 (2000) 399-411
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Heterocycles
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Ito, S.1
Ochi, N.2
Murashima, T.3
Uno, H.4
Ono, N.5
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22
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1442349803
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Shimizu Y., Shen Z., Okujima T., Uno H., and Ono N. Chem. Commun. (2004) 374-375
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Shimizu, Y.1
Shen, Z.2
Okujima, T.3
Uno, H.4
Ono, N.5
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