Hoveyda-Grubbs II structure
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Common Name | Hoveyda-Grubbs II | ||
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CAS Number | 301224-40-8 | Molecular Weight | 626.622 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C31H38Cl2N2ORu | Melting Point | 216-220ºC(lit.) | |
MSDS | USA | Flash Point | N/A |
Highly efficient ruthenium catalysts for the formation of tetrasubstituted olefins via ring-closing metathesis.
Org. Lett. 9 , 1589, (2007) [reaction: see text] A series of ruthenium-based metathesis catalysts with N-heterocyclic carbene (NHC) ligands have been prepared in which the N-aryl groups have been changed from mesityl to mono-ortho-substituted phenyl (e.g., tolyl). These new catalysts of... |
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Sequential catalysis: a metathesis/dihydroxylation sequence.
Angew. Chem. Int. Ed. Engl. 45 , 1900, (2006)
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Ruthenium catalysed cross metathesis with fluorinated olefins.
Chem. Commun. (Camb.) , 1692, (2001) The E-selective cross metathesis (CM) of fluorinated olefins with various functionalised alkenes in good to excellent yields is reported. |
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Ring-opening metathesis/oxy-cope rearrangement: a new strategy for the synthesis of bicyclic medium ring-containing compounds.
J. Am. Chem. Soc. 125 , 14901, (2003) Ring-opening/ring-closing metathesis on cyclobutene-containing substrates with angular oxygen functionality provides a stereospecific introduction of 1,5-bis-dienes required for an anion-accelerated oxy-Cope rearrangement. The reaction sequence offers general... |
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Schrodi, Y.; Pederson, R. L.
Aldrichimica Acta 40th ed.,, 45, (2007)
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Vougioukalakis, G. C.; Grubbs, R. H.
Chem. Rev. 110th ed.,, 1746, (2010)
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Grubbs, R. H.
Tetrahedron 60th ed.,, 7117, (2004)
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Trnka, T. M.; Grubbs, R. H.
Acc. Chem. Res. 34th ed.,, 18, (2001)
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Fürstner, A.
Angew. Chem. Int. Ed. Engl. 39th ed.,, 3012, (2000)
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Schuster, M.; Blechert, S.
Angew. Chem. Int. Ed. Engl. 36th ed.,, 2036, (1997)
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