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Enantioselective Transforms as T-Goals

Diisocyanoadociane, a novel marine-derived diterpenoid, was analyzed retrosynthetically using the intramolecular Diels-Alder transform as T-goal concurrently with topological and stereochemical guidance. The enantioselective synthesis outlined below allowed assignment of absolute configuration. [Pg.218]

See other pages where Enantioselective Transforms as T-Goals is mentioned: [Pg.17]    [Pg.26]    [Pg.27]    [Pg.36]    [Pg.18]    [Pg.27]    [Pg.17]    [Pg.26]    [Pg.27]    [Pg.36]    [Pg.18]    [Pg.27]    [Pg.81]    [Pg.90]    [Pg.81]    [Pg.26]    [Pg.27]    [Pg.36]    [Pg.37]    [Pg.27]    [Pg.28]   


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A enantioselective

Goals transformations

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