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Overman pyrrolidine synthesis amines

The Overman pyrrolidine synthesis is a tandem reaction, or cascade, used to generate acylpyrrolidine derivatives. This process begins with condensation of an allylic alcohol/ether-containing secondary homoallylic amine with an aldehyde, followed by an aza-Cope rearrangement and subsequent Mannich reaction. Commonly, this reaction is run in refluxing benzene with an acidic additive, such as c/-10-camphorsulfonic acid (CSA). [Pg.60]


See other pages where Overman pyrrolidine synthesis amines is mentioned: [Pg.60]    [Pg.1042]    [Pg.1042]    [Pg.216]    [Pg.62]    [Pg.1042]   
See also in sourсe #XX -- [ Pg.62 ]




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