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Jang M., Cai L., Udeani G.O., Slowing K.V., Thomas C.F., Beecher C.W.W., Fong H.H.S., Farnsworth N.R., Kinghorn A.D., Mehta R.G., Moon R.C., Pezzuto J.M. Science. 275:1997;218.
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Fong, H.H.S.7
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Chang, S.5
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For selected examples of cross metathesis of styrenes, see: (a) Crowe, W. E.; Zhang, Z. J. J. Am. Chem. Soc. 1993, 115, 10998; (b) Pietraszuk, C.; Marciniec, B.; Fischer, H. Organometallics 2000, 19, 913; (c) Choi, T.-L.; Chatterjee, A. K.; Grubbs, R. H. Angew. Chem., Int. Ed. 2001, 40, 1277.
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Zhang, Z.J.2
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For selected examples of cross metathesis of styrenes, see: (a) Crowe, W. E.; Zhang, Z. J. J. Am. Chem. Soc. 1993, 115, 10998; (b) Pietraszuk, C.; Marciniec, B.; Fischer, H. Organometallics 2000, 19, 913; (c) Choi, T.-L.; Chatterjee, A. K.; Grubbs, R. H. Angew. Chem., Int. Ed. 2001, 40, 1277.
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Organometallics
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Pietraszuk, C.1
Marciniec, B.2
Fischer, H.3
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20
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0035794963
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For selected examples of cross metathesis of styrenes, see: (a) Crowe, W. E.; Zhang, Z. J. J. Am. Chem. Soc. 1993, 115, 10998; (b) Pietraszuk, C.; Marciniec, B.; Fischer, H. Organometallics 2000, 19, 913; (c) Choi, T.-L.; Chatterjee, A. K.; Grubbs, R. H. Angew. Chem., Int. Ed. 2001, 40, 1277.
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Angew. Chem., Int. Ed.
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Choi, T.-L.1
Chatterjee, A.K.2
Grubbs, R.H.3
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21
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0035828999
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. It has been recently reported that cross metathesis of protected 2-allylphenols with styrenes afforded 1,3-diarylpropenes with moderate to good yields. See: Forget-Champagne D., Mondon M., Fonteneau N., Gesson J.-P. Tetrahedron Lett. 42:2002;7229.
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Tetrahedron Lett.
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Forget-Champagne, D.1
Mondon, M.2
Fonteneau, N.3
Gesson, J.-P.4
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For some selected examples of metathesis reactions on solid-phase, see: (a) Miller, S. J.; Blackwell, H. E.; Grubbs, R. H. J. Am. Chem. Soc. 1996, 118, 9606; (b) Schuster, M.; Lucas, N.; Blechert, S. Chem. Commun. 1997, 823; (c) Schafmeister, C. E.; Po, J.; Verdine, G. L. J. Am. Chem. Soc. 2000, 122, 5891.
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J. Am. Chem. Soc.
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Miller, S.J.1
Blackwell, H.E.2
Grubbs, R.H.3
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23
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0002847271
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For some selected examples of metathesis reactions on solid-phase, see: (a) Miller, S. J.; Blackwell, H. E.; Grubbs, R. H. J. Am. Chem. Soc. 1996, 118, 9606; (b) Schuster, M.; Lucas, N.; Blechert, S. Chem. Commun. 1997, 823; (c) Schafmeister, C. E.; Po, J.; Verdine, G. L. J. Am. Chem. Soc. 2000, 122, 5891.
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Chem. Commun.
, pp. 823
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Schuster, M.1
Lucas, N.2
Blechert, S.3
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24
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0034697649
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For some selected examples of metathesis reactions on solid-phase, see: (a) Miller, S. J.; Blackwell, H. E.; Grubbs, R. H. J. Am. Chem. Soc. 1996, 118, 9606; (b) Schuster, M.; Lucas, N.; Blechert, S. Chem. Commun. 1997, 823; (c) Schafmeister, C. E.; Po, J.; Verdine, G. L. J. Am. Chem. Soc. 2000, 122, 5891.
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J. Am. Chem. Soc.
, vol.122
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Schafmeister, C.E.1
Po, J.2
Verdine, G.L.3
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25
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0030857041
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. Ring-opening cross metathesis of bicyclic alkenes with styrenes on Wang resin has been reported. See: Cuny G.D., Cao J., Hauske J.R. Tetrahedron Lett. 38:1997;5237.
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Tetrahedron Lett.
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Cuny, G.D.1
Cao, J.2
Hauske, J.R.3
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26
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0034007951
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For some selected recent reviews on solid phase synthesis, see: (a) Wendeborn, S.; De Mesmaeker, A.; Brill, W. K.-D.; Berteina, S. Acc. Chem. Res. 2000, 33, 215; (b) Guillier, F.; Orain, D.; Bradley, M. Chem. Rev. 2000, 100, 2091; (c) Clapham, B.; Reger, T. S.; Janda, K. D. Tetrahedron 2001, 57, 4637.
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Acc. Chem. Res.
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Wendeborn, S.1
De Mesmaeker, A.2
Brill, W.K.-D.3
Berteina, S.4
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27
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0033683359
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For some selected recent reviews on solid phase synthesis, see: (a) Wendeborn, S.; De Mesmaeker, A.; Brill, W. K.-D.; Berteina, S. Acc. Chem. Res. 2000, 33, 215; (b) Guillier, F.; Orain, D.; Bradley, M. Chem. Rev. 2000, 100, 2091; (c) Clapham, B.; Reger, T. S.; Janda, K. D. Tetrahedron 2001, 57, 4637.
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Chem. Rev.
, vol.100
, pp. 2091
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Guillier, F.1
Orain, D.2
Bradley, M.3
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28
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0035962701
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For some selected recent reviews on solid phase synthesis, see: (a) Wendeborn, S.; De Mesmaeker, A.; Brill, W. K.-D.; Berteina, S. Acc. Chem. Res. 2000, 33, 215; (b) Guillier, F.; Orain, D.; Bradley, M. Chem. Rev. 2000, 100, 2091; (c) Clapham, B.; Reger, T. S.; Janda, K. D. Tetrahedron 2001, 57, 4637.
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(2001)
Tetrahedron
, vol.57
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Clapham, B.1
Reger, T.S.2
Janda, K.D.3
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29
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0011244282
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Higher yields were obtained in this reaction when the solid supported substrate was swelled at least 2 h before addition of the carbene catalyst.
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Higher yields were obtained in this reaction when the solid supported substrate was swelled at least 2 h before addition of the carbene catalyst.
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0011201365
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It is assumed that rather long and flexible olefinic moieties on resin allow site-site interactions leading to the intramolecular metathesis as in Ref. 14. However, extents of those interactions may be much less in the bound styrenyl double bonds probably due to steric reasons.
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It is assumed that rather long and flexible olefinic moieties on resin allow site-site interactions leading to the intramolecular metathesis as in Ref. 14 . However, extents of those interactions may be much less in the bound styrenyl double bonds probably due to steric reasons.
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33
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0011167105
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13C NMR, IR and HRMS.
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13C NMR, IR and HRMS.
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0011167679
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Aliphatic olefins (e.g. 1-hexene) were also reacted with the resin bound styrenyl ether with similar efficiency under otherwise identical conditions.
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Aliphatic olefins (e.g. 1-hexene) were also reacted with the resin bound styrenyl ether with similar efficiency under otherwise identical conditions.
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0030979224
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For some recent examples for synthesis of resveratrol and its derivatives, see: (a) Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95; (b) Alonso, E.; Ramón, D. J.; Yus, M. J. Org. Chem. 1997, 62, 417; (c) Guiso, M.; Marra, C.; Farina, A. Tetrahedron Lett. 2002, 43, 597.
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Carbohydr. Res.
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Orsini, F.1
Pelizzoni, F.2
Bellini, B.3
Miglierini, G.4
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36
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0031053263
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For some recent examples for synthesis of resveratrol and its derivatives, see: (a) Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95; (b) Alonso, E.; Ramón, D. J.; Yus, M. J. Org. Chem. 1997, 62, 417; (c) Guiso, M.; Marra, C.; Farina, A. Tetrahedron Lett. 2002, 43, 597.
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J. Org. Chem.
, vol.62
, pp. 417
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Alonso, E.1
Ramón, D.J.2
Yus, M.3
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37
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0037147976
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For some recent examples for synthesis of resveratrol and its derivatives, see: (a) Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95; (b) Alonso, E.; Ramón, D. J.; Yus, M. J. Org. Chem. 1997, 62, 417; (c) Guiso, M.; Marra, C.; Farina, A. Tetrahedron Lett. 2002, 43, 597.
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Tetrahedron Lett.
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, pp. 597
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Guiso, M.1
Marra, C.2
Farina, A.3
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