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Class 558/354 - Racemization, resolution, or inversion of configuration processes for optically active compounds


Subclass of Class 558 - Organic compounds -- part of the class 532-570 series
Definition: Processes wherein compounds having an asymmetric carbon
No. of patents: 83
Last issue date: 09/28/2010


1      
NumberTitleIssue Date
7803962Process for the resolution of racemic verapamil
A new process is described for the resolution of racemic verapamil, which allows the desired enantiomer to be obtained in high yields and with high enantiomeric purity. The process uses optically active 2,3-bis[(2-fluorobenzoyl)oxy]butanedioic acid as the resolving ...
09/28/2010
7301044Preparation of chiral amino-nitriles
A process and intermediates for producing 3-amino nitrites. The process involves resolving an enantiomeric mixture of chiral 3-amino nitrites in the presence of a chiral acid in a solvent system to produce a chiral 3-amino nitrile salt. The process may further compr...
11/27/2007
7232845Active substance combinations comprising insecticidal and acaricidal properties
The invention relates to novel active compound combinations of certain cyclic ketoenols and certain insecticidally active compounds that together have very good insecticidal and acaricidal properties. ...
06/19/2007
7183443Process for the preparation of enantiomerically enriched compounds
Process for the preparation of enantiomerically enriched amino aldehydes and amino alcohols, wherein a corresponding enantiomerically enriched amino nitrile is subjected to hydrogenation in the presence of hydrogen, a hydrogenation catalyst, preferably a Pd-catalyst...
02/27/2007
7097848Synergistic insecticidal mixtures
The invention relates to insecticidal mixtures comprising the compound of the formula (I) and at least one further known active compound selected from the group consisting of abamectin, emamectin or emamectin ben...
08/29/2006
7091233Active substance combinations comprising insecticidal and acaricidal properties
The invention relates to novel active compound combinations of certain cyclic ketoenols and certain insecticidally active compounds that together have very good insecticidal and acaricidal properties. ...
08/15/2006
7022869Methods of asymmetrically synthesizing enantiomers of casodex, its derivatives and intermediates thereof
Methods of synthesizing pure enantiomers of acylanalides such as Casodex® (bicalutamide) and its derivatives utilizing a compound having a ring structure that, when opened, provides a substituent having the structure of Formula I:
04/04/2006
6994866Combinations of active ingredients, which exhibit insecticidal and acaricidal properties
The invention relates to novel active compound combinations having very good insecticidal and acaricidal properties and containing (a) cyclic ketoenols having the formula  in...
02/07/2006
6730803Synthetic intermediate for epothilone derivative and production method thereof
The β-keto ester compound, β-hydroxy acid compound and acetonide form of a 1,3-diol derivative of the formulas (I), (V) and (VIII) wherein each symbol is as defined in the specification, are useful as a synthetic inter...
05/04/2004
6583306Methods of asymmetrically synthesizing enantiomers of Casodex, its derivatives and intermediates thereof
Methods of synthesizing pure enantiomers of acylanalides such as Casodex.RTM. (bicalutamide) and its derivatives utilizing a compound having a ring structure that, when opened, provides a substituent having the structure of Formula I: ##STR1## wherei...
06/24/2003
6465684Process for the separation of a mixture of enantiomers
A diastereomer complex obtained via a process for the separation of enantiomers is disclosed, wherein separation can be rapidly effected such that enantiomers are obtained with high e.e. values. The process permits the separation of mixtures of enantiomer...
10/15/2002
6235927Process for the separation of a mixture of enantiomers
A diastereomer complex obtained via a process for the separation of enantiomers is disclosed, wherein separation can be rapidly effected such that enantiomers are obtained with high e.e. values. The process pets the separation of mixtures of enantiomers i...
05/22/2001
6184381Process for preparing optically active compounds
This document describes a novel and practically excellent process for the preparation of optically active compounds, such as optically active alcohols or amines which are useful for various applications, for example, as synthetic intermediates of pharmace...
02/06/2001
5929279Preparation of Bisoximes
A process for the preparation of largely isomerically pure ଱-bisoximes of the formula Ia R1 O--N.dbd.CR2 --CR3 .dbd.N--OR4 Ia where the groups R1 O-- and R2 on the N.dbd.C bond are cis to ...
07/27/1999
5910601Chiral nitriles, their preparation and their use for the manufacture of verapamil and analogues
The subject invention concerns a process for preparing a single enantiomer, either R or S, of R'--NH--(CH2)3 --C(Ar)(CN)--R. The process is particularly useful for preparing verapamil, and analogues thereof, in single enantiomeric fo...
06/08/1999
5900503Process for producing optically active cyanohydrins
An optically active cyanohydrin represented by the following general formula (1): ##STR1## wherein each of R1 and R2 is a hydrogen atom or an amino-protecting group, and the configurations relating to the carbon atoms at the *2-position and *3-p...
05/04/1999
5892093Resolution
A reproducible process for preparing a substantially single enantiomer (R or S) of 4-cyano-4-(3,4-dimethoxyphenyl)-5-methylhexanoic acid, or an analogue thereof, thereby providing single enantiomer acid for the first time, proceeds by means of a classical...
04/06/1999
5886207Optically active compound of flubrocythrinate, a process for preparing the same
This invention relates to optically active compounds of Flubrocythrinate, their preparations and uses. The insecticidal and miticidal activities of the optically active compounds of the present invention are apparently higher than that of mixture racemic ...
03/23/1999
5821369Racemisation process
A process for the racemization of an enantiomerically-enriched compound of formula (3), comprises treatment of enantiomerically-enriched (3) with a base to obtain anion (4), optionally in protonated form, which is then combined with CH2 =CH--Y
10/13/1998
5650524Process for preparing (R)-3-amino-5-methoxychroman
A process for preparing (R)-3-amino-5-methoxychroman is provided. The process comprises the steps of (i) dissolving racemic 3-amino-5-methoxychroman and L(+)tartaric acid in water to form the tartrate salt; (ii) heating the solution until a clear solution...
07/22/1997
5648386Separation of enantiomers of cimaterol, (-)-cimaterol and the use thereof in pharmaceutical compositions and animal feeds
The invention relates to the separation of enantiomers of cimaterol, (-)-cimaterol, the addition salts thereof and processes for preparing them and their use in pharmaceutical compositions and animal feeds....
07/15/1997
5493047Method of preparing optically active cyanohydrin derivatives
The invention relates to a method of preparing an optically active cyanohydrin carboxylic acid ester from an optically active cyanohydrin of opposite configuration, wherein said starting cyanohydrin is converted with a carboxylic acid in the presence of a...
02/20/1996
5457224Resolution of racemic verapamil
A process for the resolution of racemic verapamil which comprises reacting the free base of the compound with optically active dibenzoyltartaric acid or ditoluoyltartaric acid in the molar ratio from 1:1 to 1:2 in a methanol/water mixture in the ratio fro...
10/10/1995
5395957Separation of enantiomers of cimaterol, (-)-cimaterol and the use thereof in pharmaceutical compositions and animal feeds
The invention relates to the separation of enantiomers of cimaterol, (-)-cimaterol, the addition salts thereof and processes for preparing them and their use in pharmaceutical compositions and animal feeds....
03/07/1995
5334744Isomerisation process
A process for obtaining an isomer of a compound of general formula R--CH(CN)--R' (I) wherein each of R and R' may be any organic radical linked directly or through a heteroatom to the carbon atom bearing the cyano group ...
08/02/1994
5312957Enantioselective hydrocyanation of aromatic vinyl compounds
The invention provides a process for enantioselective hydrocyanation of aromatic vinyl compounds which produces nonracemic mixtures of chiral, arylpropionitriles; novel carbohydrate phosphorus and nickel catalyst compositions; and optically pure (S)-...
05/17/1994
5278338Racemization process for optically active carboxylic acids, salts and esters
A method for racemizing an optically active carboxylic acid, or ester thereof, of the formula: ##STR1## where R1 is hydrogen, hydroxy, halo, cyano, C1 to C6 linear or branched alkoxy, amino or substituted amino or the...
01/11/1994
5241087Enantiomeric enrichment of cyanohydrins
A method of enantiomerically enriching chiral cyanohydrins is disclosed that involves selective cleavage of the unwanted enantiomer into its cleavage products HCN and the corresponding aldehyde or ketone by use of an enantioselective dehydrocyanation cata...
08/31/1993
5200561Process for producing optically active amines
Disclosed is a process for producing an optically active amine represented by the formula (IV) ##STR1## wherein R7 and R8 each denote an alkyl group, aryl group or aralkyl group, providing that they do not denote the same group ...
04/06/1993
5153349Process for the preparation of cypermethrine isomers
The invention relates to a process for the preparation of such isomer mixtures of cypermethrine of the Formula (I) ##STR1## wherein carbon atoms indicated by 1, 3 and ଱ stand for a chiral carbon atom and the wavy line indicates cis or trans con...
10/06/1992
5128497Conversion of pyrethroid isomers to more active species
Crystalline pyrethroid isomers or enantiomer pairs are converted to more pesticidally active isomers by contacting a hydrocarbon slurry of the starting isomers with an epimerization agent selected from the group consisting of 1,1,3,3-tetramethylguanidine ...
07/07/1992
5110976Insecticidal composition comprising more than one active ingredient
A process is disclosed for preparing a synergistic, crystalline product consisting of solely enantiomer pair 1RCisS and 1SCisR and enantiomer pair 1RTransS and 1STransR of cypermethrin in a 3:7 to 5:5 crystalline mixture, which comprises the steps of: (a)...
05/05/1992
5015764Preparation of optically active aliphatic carboxylic acids
A process for the separation of a racemic mixture of certain aliphatic carboxylic acids or esters thereof is disclosed. The process comprises (i) forming a salt solution comprising said racemic mixture of a C1 to C6 linear or branche...
05/14/1991
5011995Process for the preparation of optically active secondary amines
Asymmetric hydrogenation of prochiral N-aliphatic ketimines to give optically active secondary amines at a temperature from -20° to 80° C., a hydrogen pressure of 105 to 107 Pa, with the addition of catalytic amounts of an iridium ...
04/30/1991
4997970Conversion of pyrethroid isomers to move active species
Crystallizable pyrethroid isomers or enantiomer pairs are converted to more pesticidally active isomers by contacting a hydrocarbon slurry of the starting isomers with a base and a catalyst, the catalyst being substantially soluble in the slurry and selec...
03/05/1991
4962223Process for the synthesis of the levodopa
New process for the synthesis of the levodopa, L-(-)-2-amino-3-(3,4-dihydyphenyl)propionic acid, drug used in the treatment of the Parkinson's disease. The process consists in resolving with d-camphorsulfonic acid, or with a salt thereof, the d,l-2-...
10/09/1990
4910309Enrichment of optical of 2-(4-aryloxyphenoxy)-propionic acids by crystallization as hydrates
The optical purity of an optically active 2-(4-aryloxyphenoxy)propionic acid is enriched by formation of the hydrate of the enantiomer in excess and its removal from solution....
03/20/1990
4853477Separation of diastereomers of cyclopropanecarboxylic acid esters
A process for the separation of mutually diastereomeric forms of a cyclopropanecarboxylic acid ester of the formula ##STR1## in which R1 represents hydrogen or halogen, R2 represents hydrogen or halogen, R4 represents hydr...
08/01/1989
4782174Process for the preparation of certain pairs of enantiomers of ଱-cyano-3-phenoxy-4-fluorobenzyl permethrate
A process for the preparation of a mixture principally comprising the (b) 1R-3R-଱S+1S-3S-଱ and (d) 1R-3S-଱S+1S-3R-଱R enantiomers of the compound ଱-cyano-3-phenoxy-4-fluorobenzyl permethrate, comprising dissolving a mixture of all 8 ste...
11/01/1988
4749809Optically active borane complex and a method for producing an optically active alcohol derivative by the use thereof
The present invention relates to an optically active borane complex represented by the general formula, ##STR1## wherein R1 represents an aryl group, R2 represents an alkyl group and a mark * means an asymmetric carbon, and a me...
06/07/1988
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