Abstract:Structurally novel 2-azaspiro[4.5]deca-1,6,9-trien-8-ones
were
synthesized from N-(2-propyn-1-yl) amides and 1,3,5-trimethoxybenzenes
by a tandem method consisting of a Tf2O-promoted amide
activation and a TfOH-promoted Friedel–Crafts ipso-cyclization. The method offered the first example of using N-(2-propyn-1-yl) amides as substrates in both Tf2O-promoted secondary amide activation and the synthesis of azaspiro[4.5]deca-6,9-diene-8-ones.
A novel method for TfOH-promoted chemospecific C3- and
C2-olefinations
of isatins is developed, which offers the first examples of Grob fragmentation
using isatins and amides as substrates.
A novel method for TfOH-promoted chemospecific C3- and
C2-olefinations
of isatins is developed, which offers the first examples of Grob fragmentation
using isatins and amides as substrates.
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