The Baylis−Hillman Acetates as a Valuable Source for One-Pot Multistep Synthesis: A Facile Synthesis of Functionalized Tri-/Tetracyclic Frameworks Containing Azocine Moiety
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The Baylis-Hillman acetates have been conveniently transformed into tri-/tetracyclic heterocyclic frameworks containing an important azocine moiety via one-pot multistep protocol involving alkylation, reduction, and cyclization sequence.
创建时间:
2007-06-21



