GB1116432A - Biphenylyl aliphatic acids and their salts and esters - Google Patents
Biphenylyl aliphatic acids and their salts and estersInfo
- Publication number
- GB1116432A GB1116432A GB38168/65A GB3816865A GB1116432A GB 1116432 A GB1116432 A GB 1116432A GB 38168/65 A GB38168/65 A GB 38168/65A GB 3816865 A GB3816865 A GB 3816865A GB 1116432 A GB1116432 A GB 1116432A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- radical
- phenyl
- halogen atom
- sulphamoyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000002148 esters Chemical class 0.000 title abstract 4
- 150000003839 salts Chemical class 0.000 title abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 38
- -1 alkynyl radical Chemical class 0.000 abstract 18
- 239000002253 acid Substances 0.000 abstract 11
- 125000005843 halogen group Chemical group 0.000 abstract 11
- 238000000034 method Methods 0.000 abstract 9
- 150000007513 acids Chemical class 0.000 abstract 8
- 125000004953 trihalomethyl group Chemical group 0.000 abstract 8
- 238000006243 chemical reaction Methods 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 239000012442 inert solvent Substances 0.000 abstract 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 3
- 229910052783 alkali metal Inorganic materials 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 230000003301 hydrolyzing effect Effects 0.000 abstract 3
- 239000003513 alkali Substances 0.000 abstract 2
- 229910001515 alkali metal fluoride Inorganic materials 0.000 abstract 2
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 2
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 239000002585 base Substances 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 230000007062 hydrolysis Effects 0.000 abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 abstract 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 abstract 2
- 239000007858 starting material Substances 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- NNJMFJSKMRYHSR-UHFFFAOYSA-N 4-phenylbenzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=CC=C1 NNJMFJSKMRYHSR-UHFFFAOYSA-N 0.000 abstract 1
- LYINHPAEAYJDIR-UHFFFAOYSA-N 92-89-7 Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C([N+]([O-])=O)C=C1 LYINHPAEAYJDIR-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 1
- 238000003747 Grignard reaction Methods 0.000 abstract 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 1
- 229910005948 SO2Cl Inorganic materials 0.000 abstract 1
- 229910006024 SO2Cl2 Inorganic materials 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 238000000297 Sandmeyer reaction Methods 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 abstract 1
- 150000001350 alkyl halides Chemical class 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 125000001118 alkylidene group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- QRZAKQDHEVVFRX-UHFFFAOYSA-N biphenyl-4-ylacetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1C1=CC=CC=C1 QRZAKQDHEVVFRX-UHFFFAOYSA-N 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 abstract 1
- 239000012024 dehydrating agents Substances 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 239000012954 diazonium Substances 0.000 abstract 1
- 150000001989 diazonium salts Chemical class 0.000 abstract 1
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 229960000192 felbinac Drugs 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 150000004678 hydrides Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 230000000802 nitrating effect Effects 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 230000020477 pH reduction Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 229920001021 polysulfide Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229910001923 silver oxide Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012991 xanthate Substances 0.000 abstract 1
Classifications
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39555364A | 1964-09-10 | 1964-09-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1116432A true GB1116432A (en) | 1968-06-06 |
Family
ID=23563534
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB38168/65A Expired GB1116432A (en) | 1964-09-10 | 1965-09-07 | Biphenylyl aliphatic acids and their salts and esters |
GB38711/67A Expired GB1116434A (en) | 1964-09-10 | 1965-09-07 | Biphenylyl-substituted aliphatic aldehydes and their acetals |
GB38712/67A Expired GB1116435A (en) | 1964-09-10 | 1965-09-07 | Biphenylyl-substituted aliphatic alcohols and their ethers |
GB38600/67A Expired GB1116433A (en) | 1964-09-10 | 1965-09-07 | Amides of biphenylyl aliphatic acids |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB38711/67A Expired GB1116434A (en) | 1964-09-10 | 1965-09-07 | Biphenylyl-substituted aliphatic aldehydes and their acetals |
GB38712/67A Expired GB1116435A (en) | 1964-09-10 | 1965-09-07 | Biphenylyl-substituted aliphatic alcohols and their ethers |
GB38600/67A Expired GB1116433A (en) | 1964-09-10 | 1965-09-07 | Amides of biphenylyl aliphatic acids |
Country Status (9)
Country | Link |
---|---|
US (1) | US3624142A (enrdf_load_stackoverflow) |
BE (1) | BE669347A (enrdf_load_stackoverflow) |
BR (1) | BR6572746D0 (enrdf_load_stackoverflow) |
CH (1) | CH490309A (enrdf_load_stackoverflow) |
ES (1) | ES317635A1 (enrdf_load_stackoverflow) |
FR (5) | FR1460659A (enrdf_load_stackoverflow) |
GB (4) | GB1116432A (enrdf_load_stackoverflow) |
IL (1) | IL24046A (enrdf_load_stackoverflow) |
NL (1) | NL6511845A (enrdf_load_stackoverflow) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5033052B1 (enrdf_load_stackoverflow) * | 1968-10-25 | 1975-10-27 | ||
JPS5034556B1 (enrdf_load_stackoverflow) * | 1970-07-13 | 1975-11-10 | ||
US4163788A (en) | 1968-03-27 | 1979-08-07 | Ciba-Geigy Corporation | Tertiary aminoacids |
US4316850A (en) | 1968-03-27 | 1982-02-23 | Ciba-Geigy Corporation | Tertiary aminoacids |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4053639A (en) * | 1964-01-24 | 1977-10-11 | The Boots Company Limited | Therapeutically active phenylalkane derivatives |
US3674832A (en) * | 1968-08-22 | 1972-07-04 | Schering Corp | Cyclopropane carboxylic acid derivatives |
GB1268008A (en) * | 1969-07-09 | 1972-03-22 | Bdh Pharmaceuticals Ltd | ESTERS OF p-BYPHENYLYLACETIC ACID |
GB1275927A (en) * | 1969-07-16 | 1972-06-01 | Bdh Pharmaceuticals Ltd | ESTERS OF p-BIPHENYLYLACETIC ACID |
US3981905A (en) * | 1970-03-16 | 1976-09-21 | Boots Pure Drug Company Limited | 2-(Substituted phenyl) propionic acids |
US4192890A (en) * | 1970-04-15 | 1980-03-11 | Roussel Uclaf | Novel benzoylphenylacetic acid esters |
US3941821A (en) * | 1970-05-05 | 1976-03-02 | William H. Rorer, Inc. | 2-Thiosulfo biphenylylacetic acids |
US3864384A (en) * | 1970-05-05 | 1975-02-04 | Rorer Inc William H | Substituted phenylacetic acid compounds |
GB1359987A (en) * | 1970-10-12 | 1974-07-17 | Boots Co Ltd | 2-substituted biphenylyl propionic acids |
GB1437783A (en) * | 1972-09-22 | 1976-06-03 | Boots Co Ltd | 2-substituted biphenylyl acetic acids and derivatives thereof |
US4052514A (en) * | 1971-03-26 | 1977-10-04 | The Boots Company Limited | Trihalosubstituted biphenylyl propionic acids |
US3857880A (en) * | 1971-07-20 | 1974-12-31 | Schering Corp | Cyclopropane carboxylic acid derivatives |
BE787782A (fr) * | 1971-08-20 | 1973-02-19 | Thomae Gmbh Dr K | Nouveaux 4-(4-biphenylyl)-butyramides |
DE2205732A1 (de) * | 1972-02-08 | 1973-08-16 | Thomae Gmbh Dr K | Neue 4-(4-biphenylyl)-butensaeurederivate |
US4048332A (en) * | 1972-06-15 | 1977-09-13 | The Boots Company Limited | Phenylalkanoic acids |
GB1396726A (en) * | 1972-06-15 | 1975-06-04 | Boots Co Ltd | Phenylalkanoic acids |
US3987197A (en) * | 1972-08-17 | 1976-10-19 | Boehringer Ingelheim Gmbh | 3-(2'-fluoro-4-biphenylyl)-butyric acid and salts thereof |
DE2341506A1 (de) * | 1973-08-16 | 1975-02-27 | Thomae Gmbh Dr K | Neue biphenylderivate und verfahren zu ihrer herstellung |
US3957861A (en) * | 1973-11-07 | 1976-05-18 | The Upjohn Company | Biphenylylpropionic acids and esters |
GB1497044A (en) * | 1974-03-07 | 1978-01-05 | Prodotti Antibiotici Spa | Salts of phenyl-alkanoic acids |
US4035509A (en) * | 1974-04-22 | 1977-07-12 | Syntex (U.S.A.) Inc. | Methods and compositions for the use of 2-carboxy-5-oxo-5H-dibenzo[a,d]cycloheptenes, salts and esters thereof |
US4020094A (en) * | 1974-04-22 | 1977-04-26 | Syntex (U.S.A.) Inc. | 2-Substituted-5-oxo-5H-dibenzo[a,d]cycloheptenes, the salts and esters thereof, having pharmaceutical activity |
ES446581A1 (es) * | 1975-04-04 | 1977-06-16 | Boots Co Ltd | Un procedimiento para preparar acidos 2-arilpropionicos. |
US4333951A (en) * | 1977-11-15 | 1982-06-08 | A. H. Robins Company, Inc. | 2-Amino-6-biphenylacetic acids |
US4324904A (en) * | 1979-12-19 | 1982-04-13 | The Upjohn Company | Processes for the preparation of hydratropic acids and esters |
FR2498449A1 (fr) * | 1981-01-23 | 1982-07-30 | Fabre Sa Pierre | Acides halogeno biphenyl carboxyliques et leurs sels utiles en therapeutique |
US4731484A (en) * | 1985-01-18 | 1988-03-15 | The Dow Chemical Company | Haloacetyl derivatives of aromatic compounds |
FR2584403B1 (fr) * | 1985-07-08 | 1987-10-23 | Pf Medicament | Derives d'alcools primaires halogeno biphenyles utiles en therapeutique dans le traitement de l'atherosclerose |
IT1197289B (it) * | 1986-09-26 | 1988-11-30 | S I F I Societa Ind Farmaceuti | Sale di lisina dell'acido 4-bifenilacetico e sue composizioni oftalmiche |
US5663416A (en) * | 1990-05-22 | 1997-09-02 | Cortech Inc. | Oxidant sensitive and insensitive aromatic esters as inhibitors of human neutrophil elastase |
TW348175B (en) * | 1993-01-06 | 1998-12-21 | Hoechst Ag | Process for the preparation of biphenyl derivatives |
MX9603414A (es) * | 1994-02-17 | 1997-03-29 | American Home Prod | Derivados de bifenilo sustituidos como inhibidores de fosfodiesterasa. |
US5691376A (en) * | 1994-02-17 | 1997-11-25 | American Home Products Corporation | Substituted biphenyl derivatives |
US5593994A (en) * | 1994-09-29 | 1997-01-14 | The Dupont Merck Pharmaceutical Company | Prostaglandin synthase inhibitors |
AR002945A1 (es) * | 1994-11-15 | 1998-05-27 | Bayer Corp | Acidos 4-biarilbutirico o 5-biarilpentanoico sustituidos y sus derivados como inhibidores de las metaloproteasas de matriz, composicion que los contiene, y metodos para la preparacion de dichos compuestos |
US5789434A (en) * | 1994-11-15 | 1998-08-04 | Bayer Corporation | Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors |
JP4008498B2 (ja) | 1996-07-31 | 2007-11-14 | 塩野義製薬株式会社 | 新規パラテルフェニル化合物 |
US5994379A (en) * | 1998-02-13 | 1999-11-30 | Merck Frosst Canada, Inc. | Bisaryl COX-2 inhibiting compounds, compositions and methods of use |
KR100809489B1 (ko) * | 2001-10-10 | 2008-03-03 | 씨제이제일제당 (주) | 사이클로옥시게나제-2의 저해제로서 선택성이 뛰어난4'-메탄설포닐-비페닐 유도체 |
CN1944378A (zh) * | 2006-10-23 | 2007-04-11 | 广东中科药物研究有限公司 | 一种联苯乙酸氨丁三醇盐及其制备方法 |
CN106748721B (zh) * | 2016-11-17 | 2019-06-21 | 山东铂源药业有限公司 | 一种2-氯-5-碘苯甲酸的制备方法 |
CN114790141B (zh) * | 2022-05-25 | 2023-03-07 | 大连理工大学 | 一种无过渡金属催化的氯代烯丙基酯的合成方法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2921939A (en) * | 1955-11-28 | 1960-01-19 | Metal & Thermit Corp | Process for preparing alpha-substituted acetic acids |
FR1152761A (fr) * | 1956-04-07 | 1958-02-25 | Maggioni & C Spa | Procédé pour la préparation d'acides 4-diphénylyl-alkyl-acétiques |
US3043746A (en) * | 1959-11-02 | 1962-07-10 | Vismara Francesco Spa | 2-(4-biphenylyl)-delta-hexenoic acid and derivatives as anticholesterinemic agents |
US3120551A (en) * | 1961-03-20 | 1964-02-04 | Warner Lambert Pharmaceutical | 5-(4-biphenylyl)-3-methylvaleric acid and functional derivatives thereof |
-
1964
- 1964-09-10 US US395553A patent/US3624142A/en not_active Expired - Lifetime
-
1965
- 1965-07-28 IL IL24046A patent/IL24046A/en unknown
- 1965-08-31 BR BR172746/65A patent/BR6572746D0/pt unknown
- 1965-09-01 CH CH1222365A patent/CH490309A/de not_active IP Right Cessation
- 1965-09-07 GB GB38168/65A patent/GB1116432A/en not_active Expired
- 1965-09-07 GB GB38711/67A patent/GB1116434A/en not_active Expired
- 1965-09-07 GB GB38712/67A patent/GB1116435A/en not_active Expired
- 1965-09-07 FR FR30712A patent/FR1460659A/fr not_active Expired
- 1965-09-07 GB GB38600/67A patent/GB1116433A/en not_active Expired
- 1965-09-08 BE BE669347D patent/BE669347A/xx unknown
- 1965-09-09 ES ES0317635A patent/ES317635A1/es not_active Expired
- 1965-09-10 NL NL6511845A patent/NL6511845A/xx unknown
- 1965-12-06 FR FR41105A patent/FR7047M/fr not_active Expired
-
1967
- 1967-09-21 FR FR121825A patent/FR7048M/fr not_active Expired
- 1967-09-21 FR FR121826A patent/FR7008M/fr not_active Expired
- 1967-09-21 FR FR121824A patent/FR7007M/fr not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4163788A (en) | 1968-03-27 | 1979-08-07 | Ciba-Geigy Corporation | Tertiary aminoacids |
US4316850A (en) | 1968-03-27 | 1982-02-23 | Ciba-Geigy Corporation | Tertiary aminoacids |
JPS5033052B1 (enrdf_load_stackoverflow) * | 1968-10-25 | 1975-10-27 | ||
JPS5111613B1 (enrdf_load_stackoverflow) * | 1968-10-25 | 1976-04-13 | ||
JPS5111615B1 (enrdf_load_stackoverflow) * | 1968-10-25 | 1976-04-13 | ||
JPS5111616B1 (enrdf_load_stackoverflow) * | 1968-10-25 | 1976-04-13 | ||
JPS5111614B1 (enrdf_load_stackoverflow) * | 1968-10-25 | 1976-04-13 | ||
JPS5034556B1 (enrdf_load_stackoverflow) * | 1970-07-13 | 1975-11-10 |
Also Published As
Publication number | Publication date |
---|---|
GB1116434A (en) | 1968-06-06 |
FR7048M (enrdf_load_stackoverflow) | 1969-06-16 |
BE669347A (enrdf_load_stackoverflow) | 1966-03-08 |
FR1460659A (fr) | 1966-01-07 |
CH490309A (de) | 1970-05-15 |
ES317635A1 (es) | 1966-04-01 |
FR7007M (enrdf_load_stackoverflow) | 1969-06-02 |
GB1116435A (en) | 1968-06-06 |
FR7008M (enrdf_load_stackoverflow) | 1969-06-02 |
NL6511845A (enrdf_load_stackoverflow) | 1966-03-11 |
GB1116433A (en) | 1968-06-06 |
BR6572746D0 (pt) | 1973-08-07 |
FR7047M (enrdf_load_stackoverflow) | 1969-06-16 |
IL24046A (en) | 1970-03-22 |
US3624142A (en) | 1971-11-30 |
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