| Title |
Year |
Author |
Number |
| TETRAHYDROACRIDINE DERIVATIVES, PROCESSES FOR PREPARATION THEREOF (VARIANTS), TETRAHYDROACRIDINONE DERIVATIVES, DIHYDROBENZOXAROLE DERIVATIVE AND PHARMACEUTIC COMPOSITION HAVING EFFECT OF EASING OR ELIMINATING MEMORY DYSFUNCTION |
1992 |
- Gregori Majkl Shatski[Us]
- Kevin Dzhejms Kaples[Us]
- Dzhon Dik Tomer[Us]
|
RU2083564C1 |
| METHOD OF SYNTHESIS OF 9-AMINO-1,2,3,4-TETRAHYDROACRIDINE |
1992 |
- Tomas Bing Kin Li[Us]
- Kejt Eh.Goring[Us]
|
RU2076099C1 |
| METHOD OF SYNTHESIS OF HEXAHYDRO-8-METHYLPYRROLO[2,3-B]-INDOLE COMPOUNDS |
1993 |
- Dzhordzh S.K.Vong[Hk]
- Tomas B.K. Li[Us]
- Frants Vejbert[Us]
|
RU2108334C1 |
| METHOD FOR STEREOSELECTIVE PRODUCTION OF ASYMMETRICAL DERIVATIVES OF OXINDOLE |
1991 |
- Tomas Bing Kin Li[Us]
- Dzhordzh S.K. Vong[Us]
|
RU2072354C1 |
| SUBSTITUTED TETRAHYDRO-, OR HEXAHYDROCYCLOPENT/B/ INDOLES OR THEIR PHARMACEUTICALLY ACCEPTABLE ADDITIVE SALTS AND METHOD FOR THEIR PRODUCTION |
1992 |
- Khelen Khu Ong[Us]
- Dzherard Dzhozef O"Malli[Us]
- Majkl Klejton Merrimen[Us]
- Mark Gabriel' Palermo[Us]
|
RU2077530C1 |
| PROCESS FOR PREPARING ISOMERS, OR PHARMACEUTICALLY ACCEPTABLE SALTS, AND ALDEHYDE AS AN INTERMEDIATE PRODUCT IN THE 1-ALKYL, 1-ALKENYL OR 1-ALKYNYLARYL-2-AMINO-1, 3- PROPANEDIOL SYSTEM |
1991 |
- Dzhon Dzhozef Tidzheler[Us]
- Barbara Sivi Rokman[Us]
- Rassell Richard Li Khejmer[Us]
- Brajan Skott Frid[Us]
|
RU2024493C1 |
| METHOD OF SYNTHESIS OF AMINOCARBONYLCARBAMATES |
1990 |
- Ehdvard Dzhozef Glehmkovski[Us]
- Julin Chiang[Us]
- Rassel Richard Li Khejmer[Us]
|
RU2069664C1 |
| 1-ALKYL, 1-ALKENYL OR 1-ALKYNYLARYL-2-AMINO-1,3-PROPANEDIOLS OR THEIR OPTICAL ISOMERS OR PHARMACEUTICALLY ACCEPTABLE SALTS AND METHOD OF THEIR SYNTHESIS |
1992 |
- Dzhon Dzhozef Tidzheler[Us]
- Barbara Sivi Rokman[Us]
- Rassell Richard Li Khejmer[Us]
- Brajan Skott Frid[Us]
|
RU2074181C1 |
| [(ARYLALKYLPIPERIDINYL-4-YL)-METHYL]-2A,3,4,5-TETRAHYDRO-1-ONES OR THEIR ACID-ADDITIVE SALTS AND A METHOD OF THEIR PREPARING |
1992 |
- Rehjmond V.Kosli Ml.[Us]
- Bettina Shpal'[Us]
|
RU2043989C1 |
| METHOD OF SYNTHESIS OF PHYSOSTIGMINE DERIVATIVES (VARIANTS) |
1993 |
- Dzhordzh E.Lii
- Tomas B.K.Lii
- Donna M.Borek
|
RU2116307C1 |
where R - hydrogen atom, R′ - hydrogen atom or benzyl, or its pharmaceutically acceptable acid-additive salt is reduced in the presence of catalyst based on noble metal under hydrogen pressure. Process is carried out in medium of lower alkanol, at 50-100 C in the presence of lithium oxide hydrate and corresponding derivative of acridine-1-ol of the general formula (II) 
where R and 
have the same values or its pharmaceutically acceptable salt is obtained. ???EFFECT: improved method of synthesis.