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P-ABSA

The carbocyclic [6-7] core of guanacastepenes was prepared by. D. Trauner et al. using the intramolecular reaction between carbenoids derived from diazo carbonyl compounds and furans. The required diazo carbonyl substrate was synthesized using p-acetamidobenzenesulfonyl azide (p-ABSA) as the diazo-donor component in the Regitz diazo transfer reaction. [Pg.377]

See other pages where P-ABSA is mentioned: [Pg.588]    [Pg.588]    [Pg.377]    [Pg.377]    [Pg.441]    [Pg.588]    [Pg.588]    [Pg.52]    [Pg.52]    [Pg.52]   
See also in sourсe #XX -- [ Pg.377 ]



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