The oxygenation of styrene catalyzed by optically active cobalt Schiff base complexes in 2-propanol gives an enantiomer excess of l-phenylethanol. The asymmetric induction may be accomplished in two steps: addition of CoH species to styrene and decomposition of 1-phenylethyl hydroperoxide. Cobalt Sc
Conversion of 2′-hydroxychalcones to flavanones catalyzed by cobalt Schiff base complex
✍ Scribed by Kazushige Maruyama; Kimihiro Tamanaka; Akira Nishinaga; Akira Inada; Tsutomu Nakanishi
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 224 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Co(salpr) catalyzes the conversion of 2'-hydroxychalcones to flavanones in methanol under oxygen. Base catalysis by Co(salpr)(OH) produced in situ is responsible for the reaction, which is found to proceed reversibly. Cobalt(II) Schiff base complexes [ColI (SB) ] exhibit dioxygenase-like activity in aprotic solvents, whereas in protic solvents they catalyze monooxygen-
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Al~tract--A cationic latex has been prepared by emulsion copolymerization of styrene and divinylbenzene with 2 mol% of quaternary ammonium ion surfactant monomer 2. The cationic latex-bound cobalt (II) complex of N,N'-ethylenebis-(salicylaldimine-5-sodium sulphonate) 1 showed high catalytic activity
## Abstract Cobalt 2,4‐dinitrophenolate (complex **1**) based upon a __N__,__N__,__O__,__O__‐tetradentate Schiff base ligand framework was prepared. X‐ray diffraction analysis confirmed that complex **1** was triclinic species with a six‐coordinated central cobalt octahedron in the solid. Asymmetri
Substituted 2'-hydroxyacetophenone 4-bromophenylhydrazones are oxygenated readily in the presence of Co(Salpr) in ethanol to give 2-(4-bromophenylazo)-1,3\_benzodioxoles in good yield. The results