FIELD: chemical technology. SUBSTANCE: invention relates to method of epoxidation of prochiral olefin. Method involves interaction of prochiral olefin with oxygen source in the presence of salt catalyst. Epoxidation is carried out in the presence of isoquinoline N-oxide as ligand donor. Compound of formulas (IB) or (II) characterized by claim 2 of the invention claim are used as catalyst. Except for, invention proposes variant of method where interaction of prochiral olefin with oxygen source is carried out in the presence of compound of the formula (II) as salt catalyst and ligand source donating electron. EFFECT: improved method of epoxidation. 7 cl, 21 ex
Title |
Year |
Author |
Number |
BENZOPYRANS, PHARMACEUTICAL COMPOSITION BASED THEREON, AND METHOD OF MEDICAL TREATMENT |
1995 |
- Vaj Ngor Chan
- Ehlen Kejt Ehnn Morgan
- Mervin Tompson
- Dzhon Morris Ehvans
|
RU2147581C1 |
CONDENSED INDOLE DERIVATIVE OR ITS PHARMACEUTICALLY ACCEPTABLE SALT, PHARMACEUTICAL COMPOSITION SHOWING ACTIVITY OF 5-$$$-RECEPTOR ANTAGONIST |
1993 |
- Lehrami Mehri Gaster[Gb]
- Pol Adrian Vajman[Gb]
|
RU2104279C1 |
6-(SUBSTITUTED METHYLENE)PENEMS, METHOD OF PREPARING THEREOF, INTERMEDIATE PRODUCTS, AND PHARMACEUTICAL COMPOSITION |
1993 |
- Najdzhel Dzhon Perrimen Brum
- Frehnk Peter Kharrington
|
RU2133750C1 |
ANTAGONISTS OF ENDOTHELIAL RECEPTORS, PHARMACEUTICAL COMPOSITION, METHOD OF SYNTHESIS, METHOD OF INHIBITION OF ENDOTHELIAL RECEPTORS |
1992 |
- Rassell Donovan Kaznz
- Dzhon Dunkan Ehlliott
- Marija Amparo Lago
- Dzhek Dejl Liber
- Kehtrin Ehlizabet Pejshoff
|
RU2125980C1 |
HETEROCYCLIC COMPOUND OR ITS TAUTOMERIC FORM AND/OR PHARMACEUTICALLY ACCEPTABLE SALT AND/OR PHARMACEUTICALLY ACCEPTABLE SOLVATE, PHARMACEUTICAL COMPOSITION DECREASING BLOOD GLUCOSE LEVEL, METHOD OF TREATMENT AND/OR PROPHYLAXIS OF HYPOGLYCEMIC PATIENTS |
1993 |
- Dehvid Khej
- Dzhon Tomas Sajm
|
RU2134686C1 |
METHOD OF SYNTHESIS OF BIPHENYLCARBONITRILES |
1991 |
- Dehvid Ehntoni Roberts[Gb]
- Simon Tomas Rassell[Gb]
- Dzhon Dehvid Pittem[Gb]
|
RU2026285C1 |
METHOD OF TREATMENT OF STATE WHERE 5HT-LIKE AGONIST, DERIVATIVE OF TETRAHYDROCARBAZOLE IS REQUIRED, METHOD OF ITS SYNTHESIS, PHARMACEUTICAL COMPOSITION SHOWING ACTIVITY OF AGONIST OF 5HT-LIKE RECEPTORS |
1992 |
- Frehnsis Dehvid King
- Larami Mehri Gehster
- Al'Berto Dzhulio Kaumann
- Rodni Kristofer Jang
|
RU2137474C1 |
METHOD OF SYNTHESIS OF CLAVULANIC ACID OR ITS PHARMACEUTICALLY ACCEPTABLE SALTS AND ETHERS, CLAVULANIC ACID SALT WITH AMINE |
1995 |
- Majkl Allen Kuk[Gb]
- Robert Bennett Uilkins[Gb]
|
RU2081121C1 |
1,4,5-TRISUBSTITUTED IMIDAZOLE DERIVATIVES, METHODS OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF |
1996 |
- Ehdams Dzherri Leroj
- Gallager Timoti F.
- Garidzhipati Ravi Shanker
- Boem Dzheffri Charl'Z
- Sisko Dzhozef
- Li Dzhon Cheung-Lun
|
RU2196139C2 |
METHOD OF PREPARING AND/OR PURIFYING CLAVULANIC ACID OR PHARMACEUTICALLY ACCEPTABLE SALTS OR ESTERS THEREOF CLAVULANIC ACID SALT WITH AMINO ACID |
1993 |
- Majkl Allen Kuk[Gb]
- Robert Bennett Uilkins[Gb]
|
RU2105768C1 |