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1
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0033919896
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For recent reports involving 2,3-dihydro-1,4-benzodioxin derivatives, see: (a) Czompa, A.; Dinya, Z.; Antus, S.; Varga, Z. Arch. Pharm. 2000, 333, 175-180;
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Czompa, A.1
Dinya, Z.2
Antus, S.3
Varga, Z.4
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(b) Gu, W. X.; Jing, X. B.; Pan, X. F.; Chan, A. S. C.; Yang, T. K. Tetrahedron Lett. 2000, 41, 6079-6082;
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Gu, W.X.1
Jing, X.B.2
Pan, X.F.3
Chan, A.S.C.4
Yang, T.K.5
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0033533802
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(d) Bolognesi, M. L.; Budriesi, R.; Cavalli, A.; Chiarini, A.; Gotti, R.; Leonardi, A.; Minarini, A.; Poggesi, E.; Recanatini, M.; Rosini, M.; Tumiatti, V.; Melchiorre, C. J. Med. Chem. 1999, 42, 4214-4224;
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Bolognesi, M.L.1
Budriesi, R.2
Cavalli, A.3
Chiarini, A.4
Gotti, R.5
Leonardi, A.6
Minarini, A.7
Poggesi, E.8
Recanatini, M.9
Rosini, M.10
Tumiatti, V.11
Melchiorre, C.12
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84944045237
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Katrizky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford
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(e) Guillaumet, G. In Comprehensive Heterocyclic Chemistry II, 1st ed.; Katrizky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford, 1996; Vol. 6, pp. 447-463.
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Guillaumet, G.1
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8
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0001061904
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Comoy C., Benarab A., Monteil A., Leinot M., Massingham R., Guillaumet G. Med. Chem. Res. 1996;392-399.
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Comoy, C.1
Benarab, A.2
Monteil, A.3
Leinot, M.4
Massingham, R.5
Guillaumet, G.6
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Sánchez I., Pujol M.D., Guillaumet G., Massingham R., Monteil A., Dureng G., Winslow E. Sci. Pharm. 68:2000;159-164.
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Monteil, A.5
Dureng, G.6
Winslow, E.7
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12
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18544402515
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Holladay M.W., Bai H., Yihong L., Nan-Horng D., Jerome F., Ryther K.B., Wasicak J.T., Kincaid J.F., He Y., Hettinger A.-M., Huang P., Anderson D.J., Bannon A.W., Buckley M.J., Campbell J.E., Donnelly-Roberts D.L., Gunter K.L., Kim D.J.B., Kuntzweiler T.A., Sullivan J.P., Decker M.W., Arneric S.P. Bioorg. Med. Chem. Lett. 8:1998;2797-2802.
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Holladay, M.W.1
Bai, H.2
Yihong, L.3
Nan-Horng, D.4
Jerome, F.5
Ryther, K.B.6
Wasicak, J.T.7
Kincaid, J.F.8
He, Y.9
Hettinger, A.-M.10
Huang, P.11
Anderson, D.J.12
Bannon, A.W.13
Buckley, M.J.14
Campbell, J.E.15
Donnelly-Roberts, D.L.16
Gunter, K.L.17
Kim, D.J.B.18
Kuntzweiler, T.A.19
Sullivan, J.P.20
Decker, M.W.21
Arneric, S.P.22
more..
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13
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85031221079
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When DMF was used as solvent the allyloxygroup of 11 underwent spontaneous isomerization to the corresponding enol-ether.
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When DMF was used as solvent the allyloxygroup of 11 underwent spontaneous isomerization to the corresponding enol-ether.
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14
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85031224367
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3 at reflux or NaH in DMF at room temperature, a mixture of two compounds was obtained. In both cases the desired product was the minor fraction while the structure of the major fraction could not be determined.
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3 at reflux or NaH in DMF at room temperature, a mixture of two compounds was obtained. In both cases the desired product was the minor fraction while the structure of the major fraction could not be determined.
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15
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85031211647
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+: 230.
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+: 230.
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18
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85031228183
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+: 230.
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+: 230.
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19
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85031226175
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When the reaction was carried out on DMF or DMSO as solvents the yield of the process dramatically decreased.
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When the reaction was carried out on DMF or DMSO as solvents the yield of the process dramatically decreased.
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-
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21
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85031233784
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+: 231.
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+: 231.
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