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Ring-closing alkyne metathesis tungsten alkylidyne complex

At the same time, Filrstner used tungsten alkyUdene complex 150 developed by Schrock for ring-closing alkyne metathesis. He compared the reactivities of tungsten alkylidyne complex 150 and Mo(CO)6-p-ClC6H40H (Table 6.4) and showed that both catalysts work well, although a higher reaction temperature is required in the case of Mo(CO)6-p-chlorophenol. [Pg.198]

At the same time, Fiirstner and others used Schrock s tungsten alkylidyne complex 120 for ring-closing alkyne metathesis. They compared 120 with the Mo(CO)6-/>-ClC6H40H system (Table 4) in reactivity and found that... [Pg.301]

Ring-closing metathesis (RCM) is not restricted to alkenes similar reactions are also known for alkynes. The tungsten alkylidyne complex W(=CCMe3)(OCMc3)3 has been used to catalyze such reactions. Predict the structures of the cyclic products for metathesis of... [Pg.555]

J., Hrib, C.G., Jones, P.G., and Tamm, M. (2008) Preparation of cyclophanes by room-temperature ring-closing alkyne metathesis with imidazolin-2-iminato tungsten alkylidyne complexes. Org. [Pg.152]


See other pages where Ring-closing alkyne metathesis tungsten alkylidyne complex is mentioned: [Pg.475]   
See also in sourсe #XX -- [ Pg.2 ]




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Alkylidyne

Alkylidynes

Alkyne complexe

Alkyne complexes

Alkynes metathesis

Closed complex

Ring complexes

Ring metathesis

Ring-closed

Ring-closing

Ring-closing alkyne

Ring-closing alkyne metathesi

Ring-closing metatheses

Ring-closing metathesi

Tungsten alkynes

Tungsten complexes alkynes

Tungsten complexes rings

Tungsten metathesis

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