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Nitrogen ylide cyclizations rearrangement

Carbene reactions provide a versatile approach to the synthesis of five-membered nitrogen-containing rings. Of particular importance here are intramolecular insertion of a carbene into C — H and N — H bonds, addition onto multiple carbon-carbon bonds, intermediate formation of ylides as a result of carbene addition onto the heteroatom followed by rearrangement, cycloaddition, and cyclization. [Pg.107]


See other pages where Nitrogen ylide cyclizations rearrangement is mentioned: [Pg.399]    [Pg.347]    [Pg.271]    [Pg.109]    [Pg.126]    [Pg.108]    [Pg.731]    [Pg.531]    [Pg.2003]   
See also in sourсe #XX -- [ Pg.126 , Pg.127 , Pg.128 ]




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