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Aza‐Michael Addition of 5‐Substituted Tetrazole Catalysed By a Novel Nanoparticle Solid Base Catalyst Involving a Layered Zinc Hydroxide Supported on a Ferrite Core
Author(s) -
Pazoki Farzane,
Mehraban Jamshid Azarnia,
Shamsayei Maryam,
Bakhshi Bita,
Esfandiarpour Razieh,
Miraki Maryam Kazemi,
Heydari Akbar
Publication year - 2019
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201804070
Subject(s) - hydroxide , tetrazole , acetonitrile , catalysis , zinc , michael reaction , zinc ferrite , chemistry , nanoparticle , base (topology) , inorganic chemistry , polymer chemistry , organic chemistry , materials science , nanotechnology , mathematical analysis , mathematics
Fe 3 O 4 @SiO 2 @layered Zinc hydroxide (LZH) (0.85 mol %) efficiently was catalyzed the aza‐Michael reaction of 5‐substituted tetrazoles derivatives with α, β‐unsaturated carbonyl compound under reflux in acetonitrile to produce the new compounds. These new compounds were investigated for antibacterial activity and studied for the structural properties by theoretical calculations.