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Alkylations 2- trimethylsilyloxyfuran

Triisopropylsilyloxyfurans were effective nucleophiles for the vinylogous Mannich addition to iminium ions that were formed by Rh2(cap)4-catalyzed oxidation of N-alkyl groups by THYDRO <06JA5648>. A stereoselective addition of 2-trimethylsilyloxyfurans to aryl aldehydes-derived aldimines employing a chiral phosphine/Ag complex as catalyst was developed <06AG(I)7230>. The prototypical example is shown below. [Pg.178]


See other pages where Alkylations 2- trimethylsilyloxyfuran is mentioned: [Pg.305]    [Pg.104]    [Pg.178]    [Pg.140]    [Pg.293]    [Pg.634]    [Pg.634]    [Pg.305]    [Pg.344]    [Pg.331]    [Pg.104]    [Pg.634]    [Pg.293]   
See also in sourсe #XX -- [ Pg.685 , Pg.687 ]




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2- trimethylsilyloxyfuran

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