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Frank Kienzle Patents
Inventor:
Kienzle; Frank
Address:
Fluh, CH
No. of patents:
33
Patents:




Patent Number Title Of Patent Date Issued
6288280 Racemization of atropisomeric bis(phosphine oxide) compounds September 11, 2001
A process for the racemization of atropisomeric bis(phosphine oxide) compounds of formula I: ##STR1##in their (S) or (R) or non-racemic form, is useful for preparing optical active bisphosphine ligands, that form optical active complexes with transition metals. Racemization is therma
6037479 Chiral diarsine compounds March 14, 2000
Novel, chiral diarsine compounds, which are present in the (R)- or (S)- or (rac)-form, of the formula ##STR1## wherein R signifies an optionally substituted aryl from the group of phenyI, naphthyl, furyl and thienyl; C.sub.3-8 -cycloalkyl or C.sub.1-8 -alkyl;R.sup.1, R.sup.2, R.s
5072019 Process for the manufacture of 4-(2-butenylidene)-3,5,5-trimethyl-2-cyclohexen-1-one December 10, 1991
A method for the manufacture of the four geometric isomers of 4-(2-butenyl)idene)-3,5,5-trimethy-2-cyclohexen-1-one is provided. The process comprises pyrolyzing a compound of the formula ##STR1## wherein R represents lower-alkyl-oxycarbonyl, aryl-oxycarbonyl, or, preferably, low
5045567 Propanolamine derivatives having anti-diabetic effects September 3, 1991
Propanolamine derivatives of the formula ##STR1## wherein R.sup.1 is hydrogen or a group of formula ##STR2## n is the number 0 or 1; R.sup.2 and R.sup.5 are phenyl, m-halophenyl, m-trifluoromethylphenyl, thienyl or pyridyl;R.sup.3 is hydrogen or methyl;R.sup.4 is hydrogen, --CH.s
5015779 Process for the manufacture of 4-(2-butenylidene)-3,5,5-trimethyl-2-cyclohexen-1-one May 14, 1991
A method for the manufacture of the four geometric isomers of 4(2-butenylidene)-3,5,5-trimethyl-2-cyclohexen-1-one is provided. The process comprises pyrolyzing a compound of the formula ##STR1## wherein R represents lower-alkyl-oxycarbonyl, aryl-oxycarbonyl, or, preferably, lowe
4581172 Substituted pyrimido[6,1-a]isoquinolin-4-ones,pyrimido[6,1-a]benzozepin-4-ones and pyrimido[ April 8, 1986
Pyrimidone derivatives of the formula ##STR1## wherein n is the integer 1 or 0; A.sup.1 and A.sup.2 are independently methylene or mono-lower alkyl or di-lower alkyl methylene; X is methylene, mono-lower alkyl or di-lower alkyl methylene, nitrogen or lower alkyl nitrogen; R is hy
4455311 Imidazoquinazoline derivatives which inhibit the aggregation of blood platelets, inhibit gastric June 19, 1984
Imidazoquinazolines of the formula ##STR1## wherein one of R.sup.1 or R.sup.2 is hydrogen, chlorine, bromine, C.sub.1-4 -n-alkyl or C.sub.1-4 -n-alkoxy and the other is --N(R,R"), wherein R and R" are C.sub.1-4 -n-alkyl or R and R" taken together are tetramethylene or pentamethyl
4442289 4-Oxothieno[3,2-d]pyrimidine acetic acid esters April 10, 1984
Antiallergically-active pyrimidine derivatives of the formula ##STR1## wherein R.sup.1 is hydrogen, chlorine, bromine or C.sub.1-4 -alkyl, and R.sup.2 is hydrogen or methyl,prepared starting from corresponding 4-oxothieno[3,2-d]pyrimidine derivatives, are described.
4390540 Imidazoquinazolines having pharmaceutical activity June 28, 1983
Imidazoquinazolines of the formula ##STR1## wherein R.sup.1, R.sup.2 and R.sup.3 are hydrogen, halogen, C.sub.1-4 -alkyl, C.sub.1-4 -alkoxy or C.sub.2-5 -alkoxyalkyl; or two of R.sup.1, R.sup.2 and R.sup.3 on adjacent carbon atoms taken together are methylenedioxy or ethylenediox
4376121 Antiallerigically-active imidazothienopyrimidine derivatives March 8, 1983
Antiallergically-active pyrimidine derivatives of the formula ##STR1## wherein R.sup.1 is hydrogen, chlorine, bromine or C.sub.1-4 -alkyl, and R.sup.2 is hydrogen or methyl, prepared starting from corresponding 4-oxothieno-[3,2-d]pyrimidine derivatives, are described.
4208533 Synthesis of cyclopentanol June 17, 1980
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a betahexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-cy clopenta [b] furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing 11-desoxy and 11-alkyl p
4204073 Process for producing carotenoids May 20, 1980
A process for producing trimethyl oxo or hydroxy substituted cycopentenone food coloring agents including intermediates in this process.
4159386 Synthesis of cyclopentanol June 26, 1979
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing 11-desoxy and 11-alkyl pr
4156090 Polyene compounds May 22, 1979
15,15'-Didehydro-astaxanthin and ester derivatives thereof useful as coloring agents and intermediates for astaxanthin and a method for preparing astaxanthin from keto .alpha.-isophorone and intermediates therein.
4154963 Prostaglandin intermediates May 15, 1979
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing 11-desoxy and 11-alkyl p
4109086 3,6-Dihydro-2H-1,2-oxazines August 22, 1978
Dienylphosphates of the formula ##STR1## wherein each of R.sub.1 and R.sub.1' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower alkyl,Are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.
4089889 Synthesis of cyclopentanol May 16, 1978
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing 11-desoxy and 11-alkyl pr
4088645 O,O-Dialkylphosphoryloxy-2,3,5,8-tetrahydro-1H-s-triazolo[1 ,2a]pyridazine-1,3-diones May 9, 1978
Dienylphosphates of the formula ##STR1## wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower alkyl, are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activit
4087488 Cyano-4-(0,0-dialkylphosphoryloxy)-cyclohex-4-enes May 2, 1978
Dienylphosphates of the formula ##STR1## wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower akyl,Are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.
4077985 4-(O,O-Diester phosphoryloxy)cyclohex-4-en-1,2-carboxylic anhydrides March 7, 1978
Dienylphosphates of the formula ##STR1## wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower alkyl,Are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.
4074045 2H-cyclopenta[b]furan-2-ones and process for preparation February 14, 1978
Process for synthesizing the lactone, (dl) 3,3a beta-4,5,6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing 11-desoxy and 11-alkyl pr
4070378 Synthesis cyclopentanol January 24, 1978
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing 11-desoxy and 11-alkyl pr
4059577 Synthesis of cyclopentanol November 22, 1977
Process for synthesizing the lactone, (d1) 3,3a beta-4,5-6,6a- beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.alpha. and a process for preparing II-desoxy and II-alkyl
4044005 Peroxides of 2-oxo-cyclopenta[b]furans August 23, 1977
The compounds 3,3,4,5,6,6-hexahydro-4-(3-esterified or etherified-1-octenyl)-2-oxo-2H-cyclopenta[b]furan-5-oyl peroxides useful as intermediates in the preparation of prostaglandins F.sub.2 .alpha. and E.sub.2 which are known agents for inducing labor and terminating pregnancy.
4032520 Synthesis of cyclopentanol June 28, 1977
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.sub..alpha. and a process for preparing 11-desoxy and 11-alkyl
4029674 2-Oxo-2H cyclopenta[b]furans June 14, 1977
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a betahexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-cy clopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.sub..alpha. and a process for preparing 11-desoxy and 11-alkyl
4025584 1-Acetyl-3(4)-(dihydrocarbylphosphoryloxy)-cyclohex-3-enes May 24, 1977
Dienylphosphates of the formula ##STR1## wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower alkyl,Are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.
4005110 2H-Cyclopenta(b)furan-2-ones January 25, 1977
Process for synthesizing the lactone, (dl) 3,3a beta-4,5-6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.sub..alpha. and a process for preparing 11-desoxy and 11-al
4001281 2-Oxo-cyclopenta[b]furan-5.alpha.-carboxylic acid esters January 4, 1977
Process for synthesizing the lactone, (dl) 3,3a beta-4,5,6,6a beta-hexahydro-4beta(3-hydroxyl-1-trans-octenyl)-5alpha-hydroxy-2-oxo-2H-c yclopenta[b]furan, a known intermediate for producing prostaglandin E.sub.2 and F.sub.2.sub..alpha. and a process for preparing 11-desoxy and 11-alkyl
3978172 Process for the preparation of dienylphosphates August 31, 1976
Dienylphosphates of the formula ##SPC1##Wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower alkyl, are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.
3978171 Process for the preparation of dienylphosphates August 31, 1976
Dienylphosphates of the formula ##SPC1##Wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2, R.sub.3 and R.sub.4 is hydrogen or lower alkyl,Are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.
3975445 Novel polyene compounds and process therefor August 17, 1976
A novel process for the preparation of polyene compounds useful as coloring agents in foods, cosmetics, and pharmaceutical preparations. Novel polyenes are also disclosed.The present invention relates to polyene compounds. More particularly, the invention is concerned with novel caroteno
3933948 Dienylphosphates January 20, 1976
Dienylphosphates of the formula ##SPC1##Wherein each of R.sub.1 and R.sub.1 ' is lower alkyl, aryl or benzyl and each of R.sub.2,R.sub.3 and R.sub.4 is hydrogen or lower alkyl,Are useful as anthelmintic agents and as intermediates for enolphosphates having anthelmintic activity.


 
 
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