Vanadyl(IV) Acetate: An Efficient, Reusable Heterogenous Catalyst for Aza-Michael Reaction Under Solvent-Free Conditions
Vanadyl(IV) acetate [VO(OAc)2] efficiently catalyzes the conjugate addition of aliphatic, aromatic amines to α,-unsaturated carbonyl compounds in solvent-free media at room temperature to afford corresponding amino compounds in good to excellent yields. The catalyst can be recovered and reused for further cycles.
Keywords: Amines; aza-Michael reaction; solvent free; vanadyl(IV) acetate
Document Type: Research Article
Affiliations: Inorganic and Physical Chemistry Division, Indian Institute of Chemical Technology, Hyderabad, India
Publication date: 01 January 2008
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