Synthesis of triphenylpyridines via an oxidative cyclization reaction using Sr-doped LaCoO3 perovskite as a
Thu N M Le1, Son H Doan1, Phuc H Pham1
1Faculty of Chemical Engineering, HCMC University of Technology, VNU-HCM 268 Ly Thuong Kiet, District 10 Ho Chi Minh City Vietnam tungtn@hcmut.edu.vn ptsnam@hcmut.edu.vn +84 8 38637504 +84 8 38647256 extn 5681.
Abstract:
An La0.6Sr0.4CoO3 strontium-doped lanthanum cobaltite perovskite was prepared via a gelation and calcination approach and used as a heterogeneous catalyst for the synthesis of triphenylpyridines via the cyclization reaction between ketoximes and phenylacetic acids. The transformation proceeded via the oxidative functionalization of the sp3 C-H bond in phenylacetic acid. The La0.6Sr0.4CoO3 catalyst demonstrated a superior performance to that of the pristine LaCoCO3 as well as a series of homogeneous and heterogeneous catalysts. Furthermore, the La0.6Sr0.4CoO3 catalyst was facilely recovered and reused without considerable decline in its catalytic efficiency. To the best of our knowledge, the combination of ketoximes with easily available phenylacetic acids is novel.
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
Sharpless Epoxidation
Cycloaddition Reactions: MO Requirements for Thermal Activation

![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
