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1
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Look, G.C.1
Fotsch, C.H.2
Wong, C.-H.3
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0000579594
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For example see: Wong, C.-H.; Halcomb, R. L.; Ichikawa, Y.; Kajimoto; T. Angew. Chem. 1995, 107, 569; Angew. Chem., Int. Ed. Engl. 1995, 34, 521. Legler, G. Naturwissenschaften 1993, 80, 397.
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Wong, C.-H.1
Halcomb, R.L.2
Ichikawa, Y.3
Kajimoto, T.4
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3
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0029163690
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For example see: Wong, C.-H.; Halcomb, R. L.; Ichikawa, Y.; Kajimoto; T. Angew. Chem. 1995, 107, 569; Angew. Chem., Int. Ed. Engl. 1995, 34, 521. Legler, G. Naturwissenschaften 1993, 80, 397.
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Angew. Chem., Int. Ed. Engl.
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4
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0027423025
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For example see: Wong, C.-H.; Halcomb, R. L.; Ichikawa, Y.; Kajimoto; T. Angew. Chem. 1995, 107, 569; Angew. Chem., Int. Ed. Engl. 1995, 34, 521. Legler, G. Naturwissenschaften 1993, 80, 397.
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Legler, G.1
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5
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0024311992
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Anzeveno, P. B.; Creemer, L. J.; Daniel, J. K.; King, C.-H. R.; Liu, P. S. J. Org. Chem. 1989, 54, 2539.
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Creemer, L.J.2
Daniel, J.K.3
King, C.-H.R.4
Liu, P.S.5
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6
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Humphries, M.J.1
Matsumoto, K.2
White, S.L.3
Olden, K.4
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9
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-
0001485244
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-
For recent reviews about applications of ring closing olefin metathesis see: Schmalz, H.-G. Angew. Chem. 1995, 107, 1981; Angew. Chem., Int. Ed. Engl. 1995, 34, 1833. Koert, U. Nach. Chem. Tech. Lab. 1995, 43, 809.
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Schmalz, H.-G.1
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10
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33750239613
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For recent reviews about applications of ring closing olefin metathesis see: Schmalz, H.-G. Angew. Chem. 1995, 107, 1981; Angew. Chem., Int. Ed. Engl. 1995, 34, 1833. Koert, U. Nach. Chem. Tech. Lab. 1995, 43, 809.
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Angew. Chem., Int. Ed. Engl.
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-
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11
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0001264772
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For recent reviews about applications of ring closing olefin metathesis see: Schmalz, H.-G. Angew. Chem. 1995, 107, 1981; Angew. Chem., Int. Ed. Engl. 1995, 34, 1833. Koert, U. Nach. Chem. Tech. Lab. 1995, 43, 809.
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Koert, U.1
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1542763298
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Grubbs, R. H.; Miller, S. J.; Fu, G. C. Acc. Chem. Res. 1995, 28, 446.
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Grubbs, R.H.1
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Hallinan, K. O.; Crout, D. H. G.; Errington, W. J. Chem. Soc., Perkin Trans. 1 1994, 3537.
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Hallinan, K.O.1
Crout, D.H.G.2
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84989561615
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Nguyen, S. T.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1993, 115, 9858.
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Nguyen, S.T.1
Grubbs, R.H.2
Ziller, J.W.3
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17
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-
8044237114
-
-
note
-
The yields for the dihydroxylation and epoxidation steps given in Scheme 2 refer to isolated, purified main products, which were used for the next steps (see experimental). No attempts were made to determine the exact selectivities of these standard steps.
-
-
-
-
21
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0000413805
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Wada, M.; Sakurai, Y.; Akiba, K. Tetrahedron Lett. 1984, 25, 1083.
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Sakurai, Y.2
Akiba, K.3
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Schwab, P.; France, M. B.; Ziller, J. W.; Grubbs, R. H. Angew. Chem. 1995, 107, 2179; Angew. Chem., Int. Ed. Engl. 1995, 34, 2039.
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Schwab, P.1
France, M.B.2
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23
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33746236970
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Schwab, P.; France, M. B.; Ziller, J. W.; Grubbs, R. H. Angew. Chem. 1995, 107, 2179; Angew. Chem., Int. Ed. Engl. 1995, 34, 2039.
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24
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85085844515
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note
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3CH = CH).
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25
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0027996112
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