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Skaanderup and Madsen

A common procedure used to forge carbocyclic systems is represented by the ring-closing metathesis reactions exploiting various Grubbs-type carbene catalysts. Based on this cyclization technology, Skaanderup and Madsen [71], on the way to polyhydroxy-nortropane calystegines, reported the asymmetric synthesis of aminated 6a-carbahexoseptanose derivatives 311. [Pg.496]

See other pages where Skaanderup and Madsen is mentioned: [Pg.83]    [Pg.83]    [Pg.440]    [Pg.136]    [Pg.136]    [Pg.3934]    [Pg.3933]    [Pg.218]    [Pg.60]    [Pg.186]    [Pg.206]    [Pg.1049]    [Pg.101]    [Pg.101]    [Pg.534]   
See also in sourсe #XX -- [ Pg.29 , Pg.496 ]



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