| Title |
Year |
Author |
Number |
| CONDENSED HETEROCYCLIC COMPOUNDS AND SQUALENE-SYNTHETASE INHIBITORS |
1994 |
- Khidefumi Jukimasa
- Rjuiti Tozava
- Jasuo Sugijama
- Masakuni Kori
|
RU2129547C1 |
| CYCLIC AMINOCOMPOUND OR ITS PHYSIOLOGICALLY ACCEPTABLE ADDITIVE ACID SALT |
1990 |
- Goto Giiti[Jp]
- Jukimasa Khidefumi[Jp]
- Imamoto Tetsudzi[Jp]
|
RU2021989C1 |
| ANTIHYPERTRIGLYCERIDEMIC COMPOSITION (VARIANTS), METHOD OF ITS PREPARING, METHOD OF TREATMENT OR PROPHYLAXIS OF HYPERTRIGLYCERIDEMIA |
1995 |
- Jasuo Sugijama
- Khidefumi Jukimasa
|
RU2166320C2 |
| ARALKYLAMINE DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS |
1992 |
- Goto Giiti[Jp]
- Nagaoka Akinobu[Jp]
- Isikhara Judzi[Jp]
|
RU2021256C1 |
| PROCESS FOR PREPARING ARALKYLAMINE DERIVATIVES OR THEIR ACID ADDITION SALTS |
1990 |
- Giiti Goto[Jp]
- Akinobu Nagaoka[Jp]
- Judzi Isikhara[Jp]
|
RU2005717C1 |
| DERIVATIVES OF 4,1-BENZOXAZEPINE |
1993 |
- Jukimasa Khidefumi
- Tozava Rjuiti
- Kori Masakuni
- Kitano Kazuaki
|
RU2170732C2 |
| METHOD OF PRODUCING DERIVATIVES OF 2, 3, 4, 5-TETRAHYDRO-1, 5-BENZOXAZEPIN-4-ON OR HYDROCHLORIDES THEREOF |
0 |
- Khirosada Sugikhara
- Kokhej Nisikava
- Katsumi Ito
|
SU1459613A3 |
| TRIAZINE DERIVATIVES, METHODS OF THEIR SYNTHESIS, ANTIPROTOZOAN COMPOSITION, ADDITION TO ANIMAL FOOD, METHOD OF INHIBITION OF PROTOZOAN INFECTION IN ANIMALS |
1994 |
- Khideki Miki
- Koiti Ivanaga
- Tosimi Matsuno
|
RU2146674C1 |
| SULFUR-CONTAINING HETEROCYCLIC COMPOUNDS OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF |
1989 |
- Takasi Sokhda[Jp]
- Masao Tsuda[Jp]
- Ivao Jamazaki[Jp]
|
RU2041875C1 |
| BENZYLPIPERIDINE DERIVATIVES, METHOD OF PREPARATION THEREOF, PHARMACEUTICAL COMPOSITION AND METHOD OF PREPARATION THEREOF |
1995 |
- Khel'Mut Prjukher
- Rudol'F Gottshlikh
- Joakhim Lajbrok
- Kharri Shvartts
|
RU2160259C2 |
where: X - O, S or 
where: R1 - H, C1-C7-alkyl, C7-C10-aralkyl, C2-C8-alkylcarbonyl; R2 - H, C7-C10-aralkyl; A - benzene ring; K = 0-3; m = 0-5; n = 2, or its salt. Reagent 1: compound of the formula (II) 
where: Y - halide; Z - N-protective group. Reagent 2: compound of the formula (III) 
. The synthesized compounds were used as choline esterase inhibitors. EFFECT: improved method of synthesis. 21 cl, 18 tbl