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Ring closing metathesis , carbene synthesis applications

With the discovery by Grubbs of ruthenium carbene complexes such as Cl2(PCy3)2Ru=CHR, which mediate olefin metathesis under mild reaction conditions and which are compatible with a broad range of functional groups [111], the application of olefin metathesis to solid-phase synthesis became a realistic approach for the preparation of alkenes. Both ring-closing metathesis and cross-metathesis of alkenes and alkynes bound to insoluble supports have been realized (Figure 5.12). [Pg.182]

There are several important applications of the Mo-carbene complex (1) in the synthesis of natural products, illustrating the power of the ring-closing olefin metathesis. Thus, elegant syntheses of coronafacic acid, dactylol, and fluvirucin have been reported. [Pg.220]


See other pages where Ring closing metathesis , carbene synthesis applications is mentioned: [Pg.13]    [Pg.46]    [Pg.390]    [Pg.486]    [Pg.117]    [Pg.371]    [Pg.486]    [Pg.124]    [Pg.533]    [Pg.23]    [Pg.227]    [Pg.524]    [Pg.164]    [Pg.401]    [Pg.711]    [Pg.19]    [Pg.412]   
See also in sourсe #XX -- [ Pg.581 , Pg.582 ]




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Carbenes metathesis

Carbenes ring-closing metathesis

Carbenes rings

Metathesis applications

Metathesis, carbene synthesis

Ring closing metathesis , carbene synthesis

Ring metathesis

Ring-closed

Ring-closing

Ring-closing metatheses

Ring-closing metathesi

Synthesis applications

Synthesis metathesis

Synthesis ring-closing metathesis

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