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Mouse androgen, synthesis

Even for benzaldehyde, which lacks the feature of potential chelation control, the simple diastereoselectivity is within the range of d.r. 89 11- 98.5 1.5. This highly stereoselective method has been applied to the synthesis of natural products [e.g., exo-brevicomin (5) and mouse androgen (6)]. [Pg.723]

See other pages where Mouse androgen, synthesis is mentioned: [Pg.270]    [Pg.273]    [Pg.181]    [Pg.172]    [Pg.195]    [Pg.161]    [Pg.212]    [Pg.40]    [Pg.61]    [Pg.232]    [Pg.636]    [Pg.575]    [Pg.532]   
See also in sourсe #XX -- [ Pg.42 , Pg.270 ]



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