Abstract
A series of new, N-substituted azapodophyllotoxin derivatives were synthesized via
a three-component reaction of an aldehyde, an enaminone and tetronic acid in glacial
acetic acid, under microwave irradiation, without a catalyst. This new protocol has
the advantages of shorter time, higher yields, lower cost and broader substrate scope,
as well as easier operation.
Key words
microwave irradiation - tetronic acid - enaminone - N-substituted furo[3,4-b ]quinoline - azapodophyllotoxin
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