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Lombarde, L.; Taylor, R. J. K. Synthesis 1978, 131. Wadsworth, W. S.; Emmons, W. D. J. Am. Chem. Soc. 1961, 83, 1733.
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Gibson, V. C. Adv. Mater. 1994, 6, 37. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 960. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 7542. Schrock, R. H. Acc. Chem. Res. 1990, 23, 158. Breslow, D. S. Prog. Polym. Sci. 1993, 18, 1141.
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Grubbs, R.H.2
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Gibson, V. C. Adv. Mater. 1994, 6, 37. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 960. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 7542. Schrock, R. H. Acc. Chem. Res. 1990, 23, 158. Breslow, D. S. Prog. Polym. Sci. 1993, 18, 1141.
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Novak, B.M.1
Grubbs, R.H.2
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37
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0001422883
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Gibson, V. C. Adv. Mater. 1994, 6, 37. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 960. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 7542. Schrock, R. H. Acc. Chem. Res. 1990, 23, 158. Breslow, D. S. Prog. Polym. Sci. 1993, 18, 1141.
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, vol.23
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Schrock, R.H.1
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0027871953
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Gibson, V. C. Adv. Mater. 1994, 6, 37. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 960. Novak, B. M.; Grubbs, R. H. J. Am. Chem. Soc. 1988, 110, 7542. Schrock, R. H. Acc. Chem. Res. 1990, 23, 158. Breslow, D. S. Prog. Polym. Sci. 1993, 18, 1141.
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, vol.18
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Breslow, D.S.1
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39
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85034133048
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note
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Bis(tricyclohexylphosphine)benzylideneruthenium(IV) dichloride, commercially available from Fluka.
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-
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40
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85034118556
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note
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3. The norbornene monomers have characteristic vinyl protons at 6-6.2 ppm. Releasing the ring strain shifts these signals to 5.2-5.5 ppm in the polymer.
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41
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37049099042
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-1) polystyrene-derived Wadsworth-Emmons resin, see: Salvino, J. M.; Kresow, T. J.; Darnbrough, S.; Labaudiniere, R. J. Comb. Chem. 1999, 1, 134.
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(1980)
J. Chem. Soc., Perkin Trans. 1
, pp. 2516
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Cainelli, G.1
Contento, M.2
Manescalchi, F.3
Regnoli, R.4
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42
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0001867601
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-1) polystyrene-derived Wadsworth-Emmons resin, see: Salvino, J. M.; Kresow, T. J.; Darnbrough, S.; Labaudiniere, R. J. Comb. Chem. 1999, 1, 134.
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(1999)
J. Comb. Chem.
, vol.1
, pp. 134
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Salvino, J.M.1
Kresow, T.J.2
Darnbrough, S.3
Labaudiniere, R.4
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43
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85034132594
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note
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Typically, 50 mg of dry ROMPGEL would swell to 5 mL when solvated in acetonitrile.
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45
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0000476716
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Blanchette, M. A.; Choy, W.; Davis, J. T.; Essenfeld, A. P.; Masamune, S.; Roush, W. R.; Sakai, T. Tetrahedron Lett. 1984, 25, 2183.
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(1984)
Tetrahedron Lett.
, vol.25
, pp. 2183
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-
Blanchette, M.A.1
Choy, W.2
Davis, J.T.3
Essenfeld, A.P.4
Masamune, S.5
Roush, W.R.6
Sakai, T.7
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46
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85034137941
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note
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Commercially available from Fluka.
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-
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47
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85034131022
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note
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In a typical procedure, the aldehyde 4 (0.045 mmol) and Barton base (0.09 mmol) were added to the ROMPGEL (0.09 mmol) in acetonitrile (1.5 mL). After stirring for the required time, the mixture was filtered through a 200 mg silica cartridge (Alltech Associates, cat. no. 209150), the silica was washed with EtOAc (10 mL), and the combined washings were evaporated in a stream of nitrogen.
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48
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85034124095
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note
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13C NMR, GC, and HRMS.
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