Abstract:
PESTICIDAL HALOGENATED ORGANIC COMPOUNDS DERIVED FROM 1-PHENYL-2,2-DIHALOGENO ETHANOL, OF GENERAL FORMULA I: WHEREIN X1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, A HALOGEN ATOM, A NITRO GROUP, A SUBSTITUTED OR UNX2, IDENTICAL WITH X1 OR DIFFERENT FROM X1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, A HALOGEN ATOM, A SUBSTITUTED OR UNSUBSTITUTED LOWER ALKYL AND A LOWE ALKYLOXYL, X3 AND X4, IDENTICAL WITH OR DIFFERENT FROM ONE ANOTHER AND IDENTICAL WITH OR DIFFERENT FROM X1 AND/OR X2 ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND A HALOGEN ATOM, Y IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, A LOWER ALKYL, A LOWE ACYL AND A GROUP DERIVED FROM A MINERAL ACID, Z IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND A LOWER ALKYL, HAL IS SELECTED FROM THE GROUP CONSISTING OF A CHLORINE, A BROMINE AND A IODINE ATOM. SUBSTITUTED LOWER ALKYL, AND A LOWER ALKYLOXY,
WHEREIN R is selected from the group consisting of hydrogen, acyl of an organic carboxylic acid of one to 18 carbon atoms and alkyl of one to five carbon atoms which may be further substituted with an aryl, alkoxy and alkylthio which have antiandrogenic activity and their preparation and use.
WHEREIN Z IS HYDROGEN, ALKYL OF 1 TO 6 CARBON ATOMS OR TETRAHYDROPYRANYL, R IS ALKYL OF 1 TO 4 CARBON ATOMS, R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, HYDROXY, LOWER ALKANOYLOXY OF 1 TO 7 CARBON ATOMS AND HALOGEN, AND R2 IS HYDROGEN ALKYL OF 1 TO 4 CARBON ATOMS HAVING ANTI-ANDROGENIC ACTIVITY AND THEIR PREPARATION.
Abstract:
LACTONES OF 2-(CARBONYL-AMINO-METHYL)-5-HYDROXYMETHYL-3,6-DIHYDRO-2H-1,3-THIAZINE-4 -CARBOXYLIC ACIDS USEFUL AS INTERMEDIATES FOR ANTIBIOTICS OF THE C-CEPHALOSPORINE FAMILY AND THEIR PREPARATION. THE INVENTION RELATES TO NOVEL DIHYDRO-1,3-THIAZINE COMPOUNDS OF THE FORMULA
WHEREIN R IS SELECTED FROM THE GROUP CONSISTING OF ALKYL AND ARALKYL, Y IS SELECTED FROM THE GROUP CONSISTING OF -HN-AC, PHTHALIMIDO AND-NH-R'',R'' IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ALKYL AND ARALKYL AND AC IS THE ACYL RADICAL OF AN ORGANIC CARBOXYLIC ACID OF 1 TO 18 CARBON ATOMS AND TO A NOVEL PROCESS FOR THE PREPARATION OF THE SAID COMPOUNDS.
Abstract:
WHEREIN R is alkyl of one to four carbon atoms and R'' is selected from the group consisting of hydrogen, acyl of an organic carboxylic acid of one to 18 carbon atoms and an organic ether radical, a novel process for preparing the corresponding Delta 4,9,11-gonatrienes and novel intermediates produced by the said processes.
A novel process for the preparation of 7 Alpha -methyl- Delta 4,9-gonadienes of the formula
Abstract:
Novel 7 Alpha -methyl- Delta 4,11-gonadiene of the formula
WHEREIN R is alkyl of one to four carbon atoms and R'' is selected from the group consisting of hydrogen, acyl of an organic carboxylic acid of one to 18 carbon atoms and an organic ether radical which have anabolic and androgenic activities and their preparation.
Abstract:
The products are new tricyclic amino compounds and acid addition salts thereof, said tricyclic amino compounds corresponding to the general formula : WHERE X represents one of the following divalent hydrocarbon radicals : A represents a carbonyl (CO) or a hydroxymethylene (CHOH) group and R represents a monoalkylamino or a dialkylamino radical. They are very useful substances for human therapeutics, namely as antidepressants and antianxiety agents. The process for preparing compounds of formula (1) and their salts is disclosed.
Abstract:
A PROCESS FOR THE PRODUCTION OF 16A,17A-DIHYDROXY-19NOR-PROGESTERONE FROM A 3,5-IKETAL OF 4,5-SECO-ESTRANE3,5,17-TRIONE BY 17-CYANATION, 16-DEHYDRATION, METHYLATION, HYDROLYSIS OF THE KETALS, CYCLIZATION OF THE A RING AND HYDROXYLATION OF THE $16 BOND. THE INTERMEDIATES ARE ALSO PART OF THE DISCLOURE.
WHEREIN R IS SELECTED FROM THE GROUP CONSISTING OF METHYL AND ETHYL AND R'' IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, SATRUATED ALKYL OF 1 TO 5 CARBON ATOMS WHICH MAY CONTAIN A HETERO OXYGEN ATOM, UNSATURATED ALKYL OF 2 TO 5 CARBON ATOMS, CYCLOALKYL OF 3 TO 5 CARBON ATOMS WHICH MAY CONTAIN A HETERO OXYGEN ATOM, WITH THE PROVISO THAT R IS ETHYL WHEN R'' IS HYDROGEN WHCIH COMPOUNDS POSSESS ANABLOIC AND ANDROGENIC ACTIVITY. THE INVENTION ALSO RELATES TO A NOVEL PROCESS AND NOVEL INTERMEDIATES FOR THE PREPARATION OF THE COMPOUNDS OF FORMULA I.
WHEREIN N IS AN INTEGER FROM 0 TO 10 AND R IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND HYDROXYL HAVING ANTI-INFLAMMATORY ACTIVITY AND THEIR PREPARATION.