CA1089482A - Ferrocene derivatives and process for their manufacture - Google Patents
Ferrocene derivatives and process for their manufactureInfo
- Publication number
- CA1089482A CA1089482A CA279,121A CA279121A CA1089482A CA 1089482 A CA1089482 A CA 1089482A CA 279121 A CA279121 A CA 279121A CA 1089482 A CA1089482 A CA 1089482A
- Authority
- CA
- Canada
- Prior art keywords
- ferrocenoyl
- chloride
- cyclohexene
- ferrocene
- formula
- 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
- 238000000034 method Methods 0.000 title claims abstract description 26
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical class [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title abstract description 6
- -1 cycloalkenyl radical Chemical group 0.000 claims abstract description 22
- 150000001875 compounds Chemical class 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 3
- 239000000460 chlorine Substances 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 43
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical group Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 32
- 229940073584 methylene chloride Drugs 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 7
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 6
- XHYOVAWFRYHNBH-UHFFFAOYSA-N [C-]1(C=CC=C1)C(=O)C1CC=CCC1.[CH-]1C=CC=C1.[Fe+2] Chemical compound [C-]1(C=CC=C1)C(=O)C1CC=CCC1.[CH-]1C=CC=C1.[Fe+2] XHYOVAWFRYHNBH-UHFFFAOYSA-N 0.000 claims description 6
- 150000008065 acid anhydrides Chemical class 0.000 claims description 4
- 150000004820 halides Chemical class 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- REHOBOSQQYSOIL-UHFFFAOYSA-N 3-methylcyclohex-2-ene-1-carbonyl chloride Chemical compound CC1=CC(C(Cl)=O)CCC1 REHOBOSQQYSOIL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- BLIDAEBJLBAUFJ-UHFFFAOYSA-N [C-]1(C=CC=C1)C(=O)C1C(C(=CC1)C)(C)C.[CH-]1C=CC=C1.[Fe+2] Chemical compound [C-]1(C=CC=C1)C(=O)C1C(C(=CC1)C)(C)C.[CH-]1C=CC=C1.[Fe+2] BLIDAEBJLBAUFJ-UHFFFAOYSA-N 0.000 claims 2
- DRABXPZIQWYMMP-UHFFFAOYSA-N 1-propan-2-ylcyclohex-3-ene-1-carbonyl chloride Chemical compound CC(C)C1(C(Cl)=O)CCC=CC1 DRABXPZIQWYMMP-UHFFFAOYSA-N 0.000 claims 1
- DJSVUCGAZVWADH-UHFFFAOYSA-N 2,2,3-trimethylcyclopent-3-ene-1-carbonyl chloride Chemical compound CC1=CCC(C(Cl)=O)C1(C)C DJSVUCGAZVWADH-UHFFFAOYSA-N 0.000 claims 1
- CXWMHIRIXVNVQN-UHFFFAOYSA-N cyclohex-3-ene-1-carbonyl chloride Chemical compound ClC(=O)C1CCC=CC1 CXWMHIRIXVNVQN-UHFFFAOYSA-N 0.000 claims 1
- 206010022971 Iron Deficiencies Diseases 0.000 abstract description 4
- 208000024891 symptom Diseases 0.000 abstract description 3
- 238000011282 treatment Methods 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 30
- 229910052742 iron Inorganic materials 0.000 description 14
- 102000008857 Ferritin Human genes 0.000 description 9
- 108050000784 Ferritin Proteins 0.000 description 9
- 210000004185 liver Anatomy 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 7
- 238000008416 Ferritin Methods 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 108010017480 Hemosiderin Proteins 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 102000001554 Hemoglobins Human genes 0.000 description 2
- 108010054147 Hemoglobins Proteins 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- MPDDVPKGVKVHEY-UHFFFAOYSA-N CC(CC(=O)[C-]1C=CC=C1)CC(C)(C)C.[C-]1(C=CC=C1)C(CC(CC(C)(C)C)C)=O.[Fe+2] Chemical compound CC(CC(=O)[C-]1C=CC=C1)CC(C)(C)C.[C-]1(C=CC=C1)C(CC(CC(C)(C)C)C)=O.[Fe+2] MPDDVPKGVKVHEY-UHFFFAOYSA-N 0.000 description 1
- 241000861718 Chloris <Aves> Species 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 235000019759 Maize starch Nutrition 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229930003779 Vitamin B12 Natural products 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- CHEBDTAFCYCWRC-UHFFFAOYSA-N [C-]1(C=CC=C1)C(=O)C1C(=CCCC1(C)C)C.[CH-]1C=CC=C1.[Fe+2] Chemical compound [C-]1(C=CC=C1)C(=O)C1C(=CCCC1(C)C)C.[CH-]1C=CC=C1.[Fe+2] CHEBDTAFCYCWRC-UHFFFAOYSA-N 0.000 description 1
- DHUOAFNCKNFHCB-UHFFFAOYSA-N [C-]1(C=CC=C1)C(=O)C1C(C=CC(C1)C)C.[CH-]1C=CC=C1.[Fe+2] Chemical compound [C-]1(C=CC=C1)C(=O)C1C(C=CC(C1)C)C.[CH-]1C=CC=C1.[Fe+2] DHUOAFNCKNFHCB-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 229940124339 anthelmintic agent Drugs 0.000 description 1
- 239000000921 anthelmintic agent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 229940112822 chewing gum Drugs 0.000 description 1
- 235000015218 chewing gum Nutrition 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- VUSWCWPCANWBFG-UHFFFAOYSA-N cyclohex-3-ene-1-carboxylic acid Chemical compound OC(=O)C1CCC=CC1 VUSWCWPCANWBFG-UHFFFAOYSA-N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005534 hematocrit Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 210000005229 liver cell Anatomy 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 229960001708 magnesium carbonate Drugs 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000019163 vitamin B12 Nutrition 0.000 description 1
- 239000011715 vitamin B12 Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic Table
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Hematology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762623487 DE2623487A1 (de) | 1976-05-26 | 1976-05-26 | Ferrocenderivate und verfahren zu ihrer herstellung |
| DEP2623487.7 | 1976-05-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1089482A true CA1089482A (en) | 1980-11-11 |
Family
ID=5978989
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA279,121A Expired CA1089482A (en) | 1976-05-26 | 1977-05-25 | Ferrocene derivatives and process for their manufacture |
Country Status (26)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3404443A1 (de) * | 1984-02-08 | 1985-08-08 | Hartmut Prof. Dr. 1000 Berlin Köpf | Metallicenium-salze und deren verwendung als cytostatica bei der krebsbekaempfung |
| FR2667600B1 (fr) * | 1990-10-03 | 1993-07-23 | Poudres & Explosifs Ste Nale | Procede de synthese de monohalogenoalcanoylferrocenes. |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB898633A (en) * | 1957-08-12 | 1962-06-14 | Ici Ltd | Ferrocene derivatives |
| BE570298A (US07582779-20090901-C00044.png) * | 1957-08-12 | |||
| GB864197A (en) * | 1959-01-07 | 1961-03-29 | Ici Ltd | An improved process for the manufacture of monopivalylferrocene derivatives |
| BE587379A (US07582779-20090901-C00044.png) * | 1959-02-09 | |||
| US3432533A (en) * | 1966-10-28 | 1969-03-11 | Us Air Force | Perfluoroalkyl and perfluoroacyl ferrocenes |
| IL46027A (en) * | 1973-11-21 | 1977-06-30 | Fisons Ltd | Organo-metallic compounds their preparation and pharmaceutical compositions containing them |
| US3966783A (en) * | 1973-11-21 | 1976-06-29 | Fisons Limited | Compounds |
| IL48713A0 (en) * | 1975-01-15 | 1976-02-29 | Fisons Ltd | Novel ferrocene derivatives,their production and pharmaceutical compositions containing them |
-
1976
- 1976-05-26 DE DE19762623487 patent/DE2623487A1/de not_active Withdrawn
-
1977
- 1977-05-20 ES ES458993A patent/ES458993A1/es not_active Expired
- 1977-05-23 CH CH635277A patent/CH628354A5/de not_active IP Right Cessation
- 1977-05-23 NL NL7705648A patent/NL7705648A/xx not_active Application Discontinuation
- 1977-05-24 FI FI771642A patent/FI771642A/fi not_active Application Discontinuation
- 1977-05-24 IT IT23960/77A patent/IT1078979B/it active
- 1977-05-24 EG EG314/77A patent/EG12751A/xx active
- 1977-05-24 IL IL52151A patent/IL52151A0/xx unknown
- 1977-05-24 GR GR53551A patent/GR66107B/el unknown
- 1977-05-24 US US05/799,972 patent/US4141991A/en not_active Expired - Lifetime
- 1977-05-24 PH PH19808A patent/PH13868A/en unknown
- 1977-05-24 GB GB21810/77A patent/GB1558701A/en not_active Expired
- 1977-05-24 NZ NZ184186A patent/NZ184186A/xx unknown
- 1977-05-25 HU HU77HO1989A patent/HU175934B/hu unknown
- 1977-05-25 ZA ZA00773159A patent/ZA773159B/xx unknown
- 1977-05-25 AU AU25466/77A patent/AU511817B2/en not_active Expired
- 1977-05-25 DK DK228577A patent/DK228577A/da not_active Application Discontinuation
- 1977-05-25 AT AT373577A patent/AT350072B/de not_active IP Right Cessation
- 1977-05-25 IE IE1077/77A patent/IE44764B1/en unknown
- 1977-05-25 PT PT66600A patent/PT66600B/pt unknown
- 1977-05-25 CA CA279,121A patent/CA1089482A/en not_active Expired
- 1977-05-25 NO NO771827A patent/NO771827L/no unknown
- 1977-05-26 BE BE177957A patent/BE855095A/xx unknown
- 1977-05-26 FR FR7716137A patent/FR2352826A1/fr active Granted
- 1977-05-26 SE SE7706218A patent/SE7706218L/xx unknown
- 1977-05-26 JP JP6055377A patent/JPS537653A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| HU175934B (en) | 1980-11-28 |
| NO771827L (no) | 1977-11-29 |
| PT66600A (de) | 1977-06-01 |
| PH13868A (en) | 1980-10-22 |
| EG12751A (en) | 1980-03-31 |
| NZ184186A (en) | 1979-03-28 |
| GR66107B (US07582779-20090901-C00044.png) | 1981-01-16 |
| IE44764L (en) | 1977-11-26 |
| DE2623487A1 (de) | 1977-12-15 |
| AU511817B2 (en) | 1980-09-04 |
| IL52151A0 (en) | 1977-07-31 |
| JPS537653A (en) | 1978-01-24 |
| AT350072B (de) | 1979-05-10 |
| FI771642A (US07582779-20090901-C00044.png) | 1977-11-27 |
| FR2352826B1 (US07582779-20090901-C00044.png) | 1980-07-04 |
| IT1078979B (it) | 1985-05-08 |
| PT66600B (de) | 1979-01-22 |
| US4141991A (en) | 1979-02-27 |
| BE855095A (fr) | 1977-11-28 |
| SE7706218L (sv) | 1977-11-27 |
| CH628354A5 (de) | 1982-02-26 |
| DK228577A (da) | 1977-11-27 |
| AU2546677A (en) | 1978-11-30 |
| ATA373577A (de) | 1978-10-15 |
| GB1558701A (en) | 1980-01-09 |
| ZA773159B (en) | 1978-04-26 |
| IE44764B1 (en) | 1982-03-24 |
| ES458993A1 (es) | 1978-02-16 |
| FR2352826A1 (fr) | 1977-12-23 |
| NL7705648A (nl) | 1977-11-29 |
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