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3.5- Dienecarboxylic acid derivs

The first method, resolution, is unattractive unless both enantiomers are useful in synthesis. In some cases, such as the resolution of dienecarboxylic acid derivatives mentioned earlier (via the phenylethyl-ammonium salt), the resolution is efficient and provides optically pure materials in good yield.39 60,63 In certain cases, the dienyliron complex can be treated with a chiral nucleophile to give a mixture of dia-stereomers which are separated and then reconverted to enantiomerically pure dienyl complex.64 An example of this method is the resolution of complex (27 Scheme 33), via the menthyl ethers (195) and... [Pg.687]


See other pages where 3.5- Dienecarboxylic acid derivs is mentioned: [Pg.786]    [Pg.298]    [Pg.786]    [Pg.276]    [Pg.786]    [Pg.361]    [Pg.468]   


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