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0043206858
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note
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To the best of our knowledge, the cross-coupling of cycloalkenylsiloxanes has not been reported.
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4-4-i-Pr)] as the catalyst, see: Fürstner, A.; Hill, A. F.; Liebl, M.; Wilton-Ely, J. D. E. T. Chem. Commun. 1999, 601.
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(f) For asymmetric studies using chiral Mo complex as the catalyst, see: Zhu, S. S.; Cefalo, D. R.; La, D. S.; Jamieson, J. Y.; Davis, W. M.; Hoveyda, A. H.; Schrock, R. R. J. Am. Chem. Soc. 1999, 121, 8251.
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40
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0001101871
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(d) The ruthenium carbene complex 1 is more sensitive to the substitution pattern of alkenes than molybdenum catalyst 2, see: Kirkland, T. A.; Grubbs, R. H. J. Org. Chem. 1997, 62, 7310.
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0033598258
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Recently, the 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene-substituted ruthenium complex exhibited high reactivity in RCM, especially for di-, tri-, or tetra-substituted cyclic alkenes; see: Scholl, M.; Ding, S.; Lee, C. W.; Grubbs, R. H. Org. Lett. 1999, 1, 953.
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The molybdenum complex 2 is commercially available (Strem) and can be prepared according to the reported procedure with consistent purity and reactivity; see: (a) Fox, H. H.; Yap, K. B.; Robbins, J.; Cai, S.; Schrock, R. R. Inorg. Chem. 1992, 31, 2287.
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46
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0041704101
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note
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1H NMR analysis.
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