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1
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0000036185
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For reviews, see: a
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For reviews, see: (a) de Meijere, A.; Schirmer, H.; Duetsch, M. Angew. Chem., Int. Ed. 2000, 39, 3964-4002.
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de Meijere, A.1
Schirmer, H.2
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2
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(b) Barluenga, J.; Rodriguez, F.; Fañanás, F. J.; Flórez, J. Top. Organomet. Chem. 2004, 13, 59-121.
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Barluenga, J.1
Rodriguez, F.2
Fañanás, F.J.3
Flórez, J.4
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3
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(c) Barluenga, J.; Fernández-Rodríguez, M.; Aguilar, E. J. Organomet. Chem. 2005, 690, 539-587.
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J. Organomet. Chem
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Barluenga, J.1
Fernández-Rodríguez, M.2
Aguilar, E.3
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5
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0033986474
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For a review of l-metalla-1,3,5-hexatrienes, see: a
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For a review of l-metalla-1,3,5-hexatrienes, see: (a) Aumann, R. Eur. J. Org. Chem. 2000, 17-31.
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Eur. J. Org. Chem
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Aumann, R.1
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7
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0031774005
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(c) Barluenga, J.; Aznar, F.; Barluenga, S.; Fernández, M.; Martín, A.; García-Granda, S.; Piñera-Nicolás, A. Chem. Eur. J. 1998, 4, 2280-2298.
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Chem. Eur. J
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Barluenga, J.1
Aznar, F.2
Barluenga, S.3
Fernández, M.4
Martín, A.5
García-Granda, S.6
Piñera-Nicolás, A.7
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8
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0001080334
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(a) Merlic, C. A.; Burns, E. E.; Xu, D.; Chen, S. Y. J. Am. Chem. Soc. 1992, 114, 8722-8724.
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J. Am. Chem. Soc
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Merlic, C.A.1
Burns, E.E.2
Xu, D.3
Chen, S.Y.4
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10
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19044362518
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Barluenga, J.; Fenández-Rodriguez, M. A.; Aguilar, E. Org. Lett. 2002, 4, 3659-3662.
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Barluenga, J.1
Fenández-Rodriguez, M.A.2
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13
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37049113433
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Warrener, R. N.; Hammer, B. C.; Russell, R. A. J. Chem. Soc., Chem. Commun. 1981, 942-943.
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Warrener, R.N.1
Hammer, B.C.2
Russell, R.A.3
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14
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34748824297
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The anthraquinone unit is part of a large group of naturally occurring compounds with a number of different biological properties specially antitumor activity. See: Tietze, L. F, Gericke, K. M, Schuberth, I, Chem. 2007, 4563-4577 and references therein
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The anthraquinone unit is part of a large group of naturally occurring compounds with a number of different biological properties specially antitumor activity. See: Tietze, L. F.; Gericke, K. M.; Schuberth, I. Eur. J. Org. Chem. 2007, 4563-4577 and references therein.
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15
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39749133007
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The benzannulation reaction using tungsten carbenes was found less efficient. Thus, attempts to improve the yield of compound 5b using the corresponding tungsten enynylcarbene were unsuccesful
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The benzannulation reaction using tungsten carbenes was found less efficient. Thus, attempts to improve the yield of compound 5b using the corresponding tungsten enynylcarbene were unsuccesful.
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16
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0030842824
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Magnus, P.; Eisenbeis, S. A.; Fairhurst, R. A.; Iliadis, T.; Magnus, N. A.; Parry, D. J. Am. Chem. Soc. 1997, 119, 5591-5607.
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Magnus, P.1
Eisenbeis, S.A.2
Fairhurst, R.A.3
Iliadis, T.4
Magnus, N.A.5
Parry, D.6
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17
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0001141796
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Yamaguchi, M.; Hasabe, K.; Higshi, H.; Uchida, M.; Irie, A.; Minami, T. J. Org. Chem. 1990, 55, 1611-1623.
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Yamaguchi, M.1
Hasabe, K.2
Higshi, H.3
Uchida, M.4
Irie, A.5
Minami, T.6
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18
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39749110807
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Unfortunately these standard oxidation conditions were not effective in the case of the dimethoxy derivative 8c
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Unfortunately these standard oxidation conditions were not effective in the case of the dimethoxy derivative 8c.
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