Oxidation of p/o-Cresols to p/o-Hydroxybenzaldehydes Catalyzed by Metalloporphyrins with Molecular Oxygen

Author:

SHE Yuanbin,WANG Weijie,LI Guojun

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry,Biochemistry,Environmental Engineering

Reference14 articles.

1. Smith, W.E., (Dow Chemical Corporation), “Reimer-Tiemann aldehyde synthesis process”, US Pat., 4324922 (1982).

2. “The Reimer-Tiemann reaction in slightly hydrated solid-liquid medium: A new method for the synthesis of formyl and diformyl phenols”;Thoer;Synth. Commun.,1988

3. “Increased para selectivity in the Reimer-Tiemann reaction by use of polyethylene glycol as complexing agent”;Neumann;Synthesis,1986

4. “Catalytic-oxidation of 2-hydroxymethyl phenols by MnCln/M0/O2 (M=Cu, Fe)”;Sparfel;Tetrahedron,1990

5. Formanek, K., “o-Hydroxybenzaldehydes”, Eur. Pat., EP 77279 A1 (1983).

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