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Radical additions magnesium bromide etherate

The new diphenylalanine-derived oxazolidinone, 15, is particularly effective when used as an auxiliary on radical 29. The auxiliary can be used in a propagation sequence that involves radical addition followed by trapping of the addition radical with allylstannane or allylsilanes, Eq. (21). Excellent yield and diastereoselectivity are observed if the reaction is carried out in the presence of Lewis acids such as magnesium bromide or lanthanide triflates at —78°C. The reaction promoted by magnesium bromide, for example, provides a diastereomer mixture in excess of 100 1 with a yield of 85%. Sc, Yb, Y, La, or Sm triflates provide similar results in reactions usually carried out in ether. [Pg.433]


See other pages where Radical additions magnesium bromide etherate is mentioned: [Pg.101]    [Pg.435]    [Pg.313]    [Pg.86]    [Pg.1273]    [Pg.65]    [Pg.128]    [Pg.91]    [Pg.253]    [Pg.66]    [Pg.160]   
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Magnesium additions

Magnesium bromide Ether

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