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Cycloaddition precursor cyclohexanone

Retro-Mannich fragmentation of the cycloaddition product 40 (not isolated) resulted in the formation of the imine 41, which upon a new Mannich closure reaction produced the cyclohexanone derivative 42. Further manipulation of 42 resulted in the formation of 43, which had previously been reported as a precursor for vindorosine (44) [27, 28]. [Pg.288]

See other pages where Cycloaddition precursor cyclohexanone is mentioned: [Pg.304]    [Pg.192]    [Pg.653]    [Pg.95]    [Pg.178]    [Pg.241]    [Pg.66]    [Pg.83]   
See also in sourсe #XX -- [ Pg.168 , Pg.381 ]



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