Abstract:
Compounds of the general formula ##STR1## or pharmaceutically acceptable salts thereof, wherein Z is a saturated or unsaturated 3 to 6 carbon chain, m is 2 or 3, R.sub.1 is a hydrogen atom, or a straight or branched C.sub.1-4 alkyl group, R.sub.2, R.sub.3 and R.sub.13 are situated in the ortho, meta, or para position of the phenyl ring and are the same or different and selected from the following groups: H, OH, OR.sub.14, halogen, CO.sub.2 R.sub.9, CN, CF.sub.3, NO.sub.2, NH.sub.2, COCH.sub.3,OSO.sub.2 CF.sub.3,OSO.sub.2 CH.sub.3,CONR.sub.10 R.sub.11, OCOR.sub.12, wherein R.sub.9, R.sub.12 and R.sub.14 is a straight or branched C.sub.1-4 alkyl group, R.sub.10 and R.sub.11 are the same or different and represents hydrogen or a straight or branched C.sub.1-6 alkyl group, R is 1) ##STR2## processes for their preparation, pharmaceutical preparations containing them and the use of the compounds in the treatment psychiatric disorders.
Abstract:
Compounds of the formula ##STR1## wherein R.sup.1 and R.sup.3 each is hydrogen or R.sup.1 and R.sup.3 together form a second carbon-to-nitrogen bond, R.sup.2 is hydrogen or cyano, R.sup.4 is alkyl and Ar is one of certain aromatic moieties.The compounds can be used as abscission agents for the loosening of fruit and/or leaves on plants.
Abstract:
A process the preparation of a dithiocarboxylic esters comprises reacting a carboxylic acid compound of formula R1(COOH)m, a compound of formula R2AH and phosphorus pentasulfide to produce a compound of structure I. An alternate process comprises reacting a 1 compound of formula R3(COAH)m and a compound of structure II 2 in the presence of a clay catalyst; and treating products of the reaction with a thiating agent to produce a compound of structure III, a compound of structure IV, or a combination of compounds of structure III and structure IV. 3
Abstract:
The compounds disclosed are of the formula ##STR1## and the anhydrides thereof wherein R.sub.f is a perfluoroalkyl group,R' is a divalent group of alkylene, ether, thioether or a sec.amine,Y is oxygen, sulfur or an amine, andR is hydrogen or alkyl.R.sup.3 is hydrogen or methylThese compounds can be prepared by a free radical catalyzed addition of a polyfluoroalkylthiol to a 5-norbornene diacid or its derivative. They are useful in preparing surfactants when reacted with an amine.
Abstract:
The compounds disclosed are of the formula ##STR1## and the anhydrides thereof WHEREINR.sub.f is a perfluoroalkyl group,R' is a divalent group of alkylene, ether, thioether or a sec.amine,Y is oxygen, sulfur or an amine, andR is hydrogen or alkyl.R.sup.3 is hydrogen or methylThese compounds can be prepared by a free radical catalyzed addition of a polyfluoroalkylthiol to a 5-norbornene diacid or its derivative. They are useful in preparing surfactants when reacted with an amine.
Abstract:
The compounds disclosed are of the formula ##STR1## and the anhydrides thereof WHEREINR.sub.f is a perfluoroalkyl group,R' is a divalent group of alkylene, ether, thioether or a sec.amine,Y is oxygen, sulfur or an amine, andR is hydrogen or alkyl.R.sup.3 is hydrogen or methylThese compounds can be prepared by a free radical catalyzed addition of a polyfluoroalkylthiol to a 5-norbornene diacid or its derivative. They are useful in preparing surfactants when reacted with an amine.
Abstract:
The compounds disclosed are of the formula ##SPC1##And the anhydrides thereofWhereinR.sub.f is a perfluoroalkyl group,R' is a divalent group of alkylene, ether, thioether or a sec.amine,Y is oxygen, or an amine, andR is hydrogen or alkyl.R.sup.3 is hydrogen or methylThese compounds can be prepared by a free radical catalyzed addition of a polyfluoroalkylthiol to a 5-norbornene diacid or its derivative. They are useful in preparing surfactants when reacted with an amine.