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O hindered

The most obvious way is a halogenation in add solution (Chapter 21) on the more substituted side of the ketone and elimination of HX in base. The double bond uhll prefer to go inside the ring and there is no argument about its stereoehcmistn. Typical bases would he tertiary amines o hindered alkoxides (c.g. t-RuO ). [Pg.262]


See other pages where O hindered is mentioned: [Pg.49]    [Pg.1543]    [Pg.1787]    [Pg.302]   
See also in sourсe #XX -- [ Pg.29 , Pg.184 ]




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Hindered

O-H bonds in sterically hindered phenols

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