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RCM/tautomerization

There are many aromatic compounds that are in equilibrium with their tautomers. Therefore, it is possible to target the tautomers as direct RCM products for the synthesis of aromatic compounds. Scheme 26.19 shows an RCM/tautomerization sequence used to synthesize naphthol 68 by van Otterlo et al. [25]. The direct product by RCM of diene 66, which contains a carbonyl group, was ketonic tautomer... [Pg.730]

See other pages where RCM/tautomerization is mentioned: [Pg.730]    [Pg.732]   
See also in sourсe #XX -- [ Pg.730 , Pg.732 ]



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