141 |
CYCLOHEXANDIONECARBOXYLIC ACID DERIVATIVES HAVING A HERBICIDAL AND PLANT GROWTH-REGULATING ACTION. |
MYPI19872263 |
1987-09-29 |
MY102084A |
1992-03-31 |
HANS-GEORG BRUNNER |
NEW CYCLOHEXANEDIONECARBOXYLIC ACID DERIVATIVES EXHIBIT A HERBICIDAL AND PLANT GROWTH-REGULATING ACTION. THE CYCLOHEXANEDIONECARBOXYLIC ACID DERIVATIVES CORRESPONDING (SIC) TO THE FORMULA 1 WHEREIN A DENOTES A RADICAL -OR2 OR -NR3R4,B DENOTES HYDROXYL, A RADICAL -NHOR1 OR A METAL OR AMMONIUM SALT THEREOF R DENOTES C1-C6-ALKYL, C1-C6-CYCLOALKYL WHICH IS UNSUBSTITUTED OR SUBSTITUTED BY HALOGEN, C1-C4-ALKOXYL OR C1-C4 ALKYLTHIO,R1 DENOTES C1-C6-ALKYL, C1-C6-HALOGENOALKYL, C3-C6-ALKENYL, C3-C6-HALOGENOALKENYL OR C3-C6-ALKYNYL,R2 R3 AND R4 INDEPENDENTLY OF ONE ANOTHER EACH DENOTEHYDROGEN; CI-C6 ALKYL, C1-C6-HALOGENOALKYL, C2-C10-ALKOXYALKYL OR C2-C10-ALKYLTHIOALKYL; C3-C6-ALKENYL WHICH IS UNSUBSTITUTED OR SUBSTITUTED BY HALOGEN, C1-C4-ALKOXY OR C1-C4-ALKYLTHIO; C3-C6-ALKYNYL; OR PHENYL OR C1-C6 ARALKYL WHEREIN THE PHENYL NUCLEUS IS UNSUBSTITUTED OR SUBSTITUTED BY HYDROGEN, C1-C4-ALKYL, C1-C4-ALKOXY, C1-C4-HALOGENOALKYL, NITRO OR CYANO, AND R3 ANDR4, TOGETHER WITH THE NITROGEN ATOM TO WHICH THEY ARE ATTACHED, ALSO FORM A 5-MEMBERED TO 6-MEMBERED HETEROCYCLIC STRUCTURE WHICH CAN BE ALSO CONTAIN AN OXYGEN OR SULFUR ATOM IN THE RING. |
142 |
Inhibitors of slow reacting substance anaphylactic. |
DE3585377 |
1985-07-11 |
DE3585377D1 |
1992-03-26 |
SAKSENA ANIL KUMAR; WONG JESSE KWOK-KEUNG; MANGIARACINA PIETRO |
|
143 |
RETINOIDS,THEIR MANUFACTURE AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
IL8404187 |
1987-09-30 |
IL84041A |
1992-02-16 |
|
|
144 |
|
NO841687 |
1984-04-27 |
NO168526B |
1991-11-25 |
CRAWLEY GRAHAM CHARLES; EDWARDS PHILIP NEIL; HILL GEORGE BERESFORD; TAIT BRIAN STEELE; YOUNG DEREK WILLIAM; PILGRIM WILLIAM ROBERT |
|
145 |
ORGANIC SULFIDE ANTIOXIDANTS |
CA2027829 |
1990-10-17 |
CA2027829A1 |
1991-05-01 |
BOHEN JOSEPH M; REILLY JAMES L |
ORGANIC SULFIDE ANTIOXIDANTS Organic sulfide antioxidants useful for stabilizing polyolefins against oxidative and thermal degradation during processing and use represented by Formula I: (I) wherein n is an integer of 2 to 15; R is an integer group of 2 to 30 carbons, or a cycloalkyl group of 5 to 20 carbons, R is a substituted or unsubstituted alkyl group of 2 to 30 carbons, a substituted or unsubstituted cycloalkyl group of 5 to 20 carbons, a substituted or unsubstituted alkyl group of 2 to 30 carbons where any of up to 6 carbon atoms are replaced with an O or S heteroatom, a substituted or unsubstituted cycloalkyl group of 5 to 20 carbons where any of up to 6 carbon atoms are replaced with an O or S heteroatom, with the proviso that the heteroatoms must be separated from each other and from the portion of the compound to which the R group is bonded by at least one carbon atom, the substituents for R being -OH, -SR4 or -OR4, wherein R4 is an alkyl group of 1 to 3 0 carbons or a cycloalkyl group of 5 to 20 carbons; R1 and R2 are independently H or an alkyl group of 1 to 4 carbons; and R3 is an alkyl group of 1 to 24 carbons or a cycloalkyl group of 5 to 20 carbons. |
146 |
RETROVIRAL PROTEASE INHIBITING COMPOUNDS |
AU5571190 |
1990-05-18 |
AU5571190A |
1990-11-29 |
NAME NOT GIVEN |
|
147 |
|
AT86303299 |
1986-04-30 |
ATE56951T1 |
1990-10-15 |
KOJIMA KOICHI; AMEMIYA SHIGEO; KOYAMA KAZUO; IWATA NOBUYOSHI; OSHIMA TAKESHI |
|
148 |
PROSTAGLANDIN DERIVATIVES, THEIR PREPARATION AND USE |
CA508019 |
1986-04-30 |
CA1273919A |
1990-09-11 |
KOJIMA KOICHI; AMEMIYA SHIGEO; KOYAMA KAZUO; IWATA NOBUYOSHI; OSHIMA TAKASHI |
Prostaglandin derivatives, and specifically derivatives of isocarbacyclin, have an optionally substituted methylene group as a substituent on the .alpha.-carbon atom of the .alpha.-side chain. They have a variety of physiological effects, notably a strong ability to inhibit blood platelet aggregation and a strong anti-ulcer activity. They may be prepared from a carbacyclin derivative. |
149 |
HERBICIDES AND REGULATING THE GROWTH OF PLANTS COMPOSITIONS CONTAINING AS ACTIVE SUBSTANCE DERIVATIVES OF CYCLOHEXAN-DION-CARBONIC ACID AND PROCESS FOR PRODUCTION OF THE ACTIVE SUBSTANCES |
HU190384 |
1984-05-17 |
HU199770B |
1990-03-28 |
BRUNNER HANS-GEORG |
|
150 |
PROCESS FOR PRODUCING FLUOROALLYLAMINE MONOAMINEOXIDASE INHIBITORS |
HU502586 |
1986-12-04 |
HU199394B |
1990-02-28 |
BEY PHILIPPE; MCDONALD IAN A; PALFREYMAN MICHAEL G |
|
151 |
|
NO844570 |
1984-11-15 |
NO160361C |
1989-04-12 |
BRUNNER HANS-GEORG |
|
152 |
|
ES557713 |
1987-09-01 |
ES557713A0 |
1989-03-16 |
|
|
153 |
CYCLOHEXANEDIONE-CARBOXYLIC-ACID DERIVATIVES HAVING A HERBICIDAL AND PLANT GROWTH REGULATING ACTIVITY |
DE3476195 |
1984-05-14 |
DE3476195D1 |
1989-02-23 |
BRUNNER HANS-GEORG |
|
154 |
|
PT8386486 |
1986-12-03 |
PT83864B |
1989-01-17 |
BEY PHILIPPE; PALFREYMAN MICHAEL G; MCDONALD IAN A |
|
155 |
DERIVATIVES OF 4-ACYL-3,5-DIOXOCYCLO HEXANECARBOXYLIC ACID,THEIR PREPARATION AND THEIR USE AS HERBICIDES AND PLANT GROWTH REGULATORS |
IL7184984 |
1984-05-16 |
IL71849A |
1988-06-30 |
|
|
156 |
UN PROCEDIMIENTO PARA LA PREPARACION DE NUEVOS DERIVADOS DE PROSTAGLANDINA |
ES557711 |
1987-09-01 |
ES8802418A1 |
1988-06-01 |
|
LOS DERIVADOS DE PROSTAGLANDINA (I), DONDE NO EXCLUSIVAMENTE R ELEVADO A 1 ES CARBOXI O TETRAZOLILO, R ELEVADO A 2, R ELEVADO A 3 Y R ELEVADO A 6 ALQUILO C1-4, R ELEVADO A 4 Y R ELEVADO A 5 ACILO ALIFATICO C2-5, O ACILO AROMATICO, R ELEVADO A 7 ALQUILO C1-12, B ES -CH2-CH2 O -CH=CH-, E OXIGENO O AZUFRE, P VA DE 0 A 3 Y Q DE 1 A 3, Y LA LINEA DISCONTINUA REPRESENTA UN DOBLE ENLACE EN 2 O 3; SE OBTIENE HACIENDO REACCIONAR UN COMPUESTO (II) CON HALOGENURO (III) O AGENTE SULFONILANTE (IV) CUANDO E ES AZUFRE Y OPCIONALMENTE TRANSFORMAR LOS GRUPOS R ELEVADO A 15-, -OR ELEVADO A 11 Y OTROS EN R ELEVADO A 1, -OR ELEVADO A 4 Y OTROS. ESTOS DERIVADOS, ESPECIFICAMENTE LOS DE ISOCARBACICLINA, INHIBEN FUERTEMENTE LA AGRUPACION DE PLAQUETAS EN SANGRE Y PRESENTAN FUERTE ACTIVIDAD ANTIULCERA. *FORMULA* |
157 |
|
ES557712 |
1987-09-01 |
ES557712A0 |
1988-06-01 |
|
|
158 |
HERBICIDE AND GROWTH-CONTROLLING COMPOSITIONS CONTAINING ACYL-CYCLOHEXANE-DIONS AND OKSIMETHERS THEREOF AS ACTIVE COMPONENTS AND PROCESS FOR PRODUCING THE ACTIVE COMPONENTS |
HU175887 |
1987-04-23 |
HUT44121A |
1988-02-29 |
TOBLER HANS |
|
159 |
PHENOL DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS |
NZ20797584 |
1984-04-27 |
NZ207975A |
1987-11-27 |
CRAWLEY G C; EDWARDS P N; HILL G B; PILGRIM W R; TAIT B S; YOUNG D W |
|
160 |
UN PROCEDIMIENTO PARA LA PREPARACION DE NUEVOS DERIVADOS DE PROSTAGLANDINA. |
ES554621 |
1986-04-30 |
ES8800665A1 |
1987-11-16 |
|
PROCEDIMIENTO PARA PREPARAR NUEVOS DERIVADOS DE PROSTAGLANDINA. COMPRENDE: A) HACER REACCIONAR A (III) CON CLORURO DE BENCENO, EN PRESENCIA DE TRIETILAMINA EN HEXANO Y ENTRE C30J Y B50JC; B) TRATAR AL COMPUESTO DE A) CON TRIETILAMINA, EN HEXANO Y ENTRE 0J Y 80JC, PARA DAR A (III) Y C) REDUCIR A (III) CON SULFURO SODICO, EN ALCOHOL Y ENTRE 0J Y 100JC, PARA OBTENER A (I) Y SUS SALES Y ESTERES FARMACEUTICAMENTE ACEPTABLES. SIENDO: AK, ALQUILENO DE CADENA LINEAL Y DE C 1 A 4; B, -CH2-CH2O -CHFCN-; R1, CARBOXI, TETRAZOLILO Y OTROS; R2, R3 Y R6, H O ALQUILO DE C 1 A 4; R4 Y R5, -R10; R7 Y R7A, ALQUILO DE C 1 A 12; R11 Y R12 GRUPO PROTECTOR DE HIDROXI Y R14, TETRAZOLILO. SE UTILIZAN COMO ANTIULCEROSOS. |