GB1286775A - Bis-basic ketones of fluorene and fluorenone - Google Patents
Bis-basic ketones of fluorene and fluorenoneInfo
- Publication number
- GB1286775A GB1286775A GB24584/71A GB2458471A GB1286775A GB 1286775 A GB1286775 A GB 1286775A GB 24584/71 A GB24584/71 A GB 24584/71A GB 2458471 A GB2458471 A GB 2458471A GB 1286775 A GB1286775 A GB 1286775A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fluorene
- compounds
- bis
- reacting
- chloride
- 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
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 title abstract 8
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 title 1
- 150000002576 ketones Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 150000008376 fluorenones Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- JFDPFFPIDFOXQF-UHFFFAOYSA-N 9h-fluorene-1,7-dicarbonitrile Chemical compound C1=CC=C(C#N)C2=C1C1=CC=C(C#N)C=C1C2 JFDPFFPIDFOXQF-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- 230000001590 oxidative effect Effects 0.000 abstract 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- FWYDVUVWJDWWQH-UHFFFAOYSA-N 1-(1-acetyl-9h-fluoren-2-yl)ethanone Chemical compound C1=CC=C2C3=CC=C(C(=O)C)C(C(C)=O)=C3CC2=C1 FWYDVUVWJDWWQH-UHFFFAOYSA-N 0.000 abstract 1
- HDDNBUNZJIQDBQ-UHFFFAOYSA-N 1-(3-chloropropyl)piperidine Chemical compound ClCCCN1CCCCC1 HDDNBUNZJIQDBQ-UHFFFAOYSA-N 0.000 abstract 1
- ZRAYZXCFSZCTKV-UHFFFAOYSA-N 2,7-bis(2-chloroacetyl)fluoren-9-one Chemical compound C1=C(C(=O)CCl)C=C2C(=O)C3=CC(C(=O)CCl)=CC=C3C2=C1 ZRAYZXCFSZCTKV-UHFFFAOYSA-N 0.000 abstract 1
- CHXBGIFCBBODIH-UHFFFAOYSA-N 2-chloro-1-[7-(2-chloroacetyl)-9h-fluoren-2-yl]ethanone Chemical compound ClCC(=O)C1=CC=C2C3=CC=C(C(=O)CCl)C=C3CC2=C1 CHXBGIFCBBODIH-UHFFFAOYSA-N 0.000 abstract 1
- RWEWOTNIAMNBPI-UHFFFAOYSA-N 4-chloro-1-[7-(4-chloro-2-methylbutanoyl)-9h-fluoren-2-yl]-2-methylbutan-1-one Chemical compound ClCCC(C)C(=O)C1=CC=C2C3=CC=C(C(=O)C(CCCl)C)C=C3CC2=C1 RWEWOTNIAMNBPI-UHFFFAOYSA-N 0.000 abstract 1
- VDULZBPMPRKRHA-UHFFFAOYSA-N 4-chloro-1-[7-(4-chlorobutanoyl)-9h-fluoren-2-yl]butan-1-one Chemical compound ClCCCC(=O)C1=CC=C2C3=CC=C(C(=O)CCCCl)C=C3CC2=C1 VDULZBPMPRKRHA-UHFFFAOYSA-N 0.000 abstract 1
- ZBTODGZAWCMSBO-UHFFFAOYSA-N 4-chloro-1-[7-(4-chloropentanoyl)-9h-fluoren-2-yl]pentan-1-one Chemical compound CC(Cl)CCC(=O)C1=CC=C2C3=CC=C(C(=O)CCC(Cl)C)C=C3CC2=C1 ZBTODGZAWCMSBO-UHFFFAOYSA-N 0.000 abstract 1
- LJXFUBMDMUVZKA-UHFFFAOYSA-N 4-chloro-2-methylbutanoyl chloride Chemical compound ClC(=O)C(C)CCCl LJXFUBMDMUVZKA-UHFFFAOYSA-N 0.000 abstract 1
- CDIIZULDSLKBKV-UHFFFAOYSA-N 4-chlorobutanoyl chloride Chemical compound ClCCCC(Cl)=O CDIIZULDSLKBKV-UHFFFAOYSA-N 0.000 abstract 1
- HCBIDLRKPXILPU-UHFFFAOYSA-N 4-chloropentanoyl chloride Chemical compound CC(Cl)CCC(Cl)=O HCBIDLRKPXILPU-UHFFFAOYSA-N 0.000 abstract 1
- SDTOOKYSKBGYTK-UHFFFAOYSA-N 5-chloro-1-[7-(5-chloro-3-methylpentanoyl)-9h-fluoren-2-yl]-3-methylpentan-1-one Chemical compound ClCCC(C)CC(=O)C1=CC=C2C3=CC=C(C(=O)CC(CCCl)C)C=C3CC2=C1 SDTOOKYSKBGYTK-UHFFFAOYSA-N 0.000 abstract 1
- AAOVCKJZAXIUSW-UHFFFAOYSA-N 5-chloro-1-[7-(5-chloropentanoyl)-9h-fluoren-2-yl]pentan-1-one Chemical compound ClCCCCC(=O)C1=CC=C2C3=CC=C(C(=O)CCCCCl)C=C3CC2=C1 AAOVCKJZAXIUSW-UHFFFAOYSA-N 0.000 abstract 1
- KBOGMBQWZCIHNQ-UHFFFAOYSA-N 5-chloro-3-methylpentanoyl chloride Chemical compound ClCCC(C)CC(Cl)=O KBOGMBQWZCIHNQ-UHFFFAOYSA-N 0.000 abstract 1
- SVNNWKWHLOJLOK-UHFFFAOYSA-N 5-chloropentanoyl chloride Chemical compound ClCCCCC(Cl)=O SVNNWKWHLOJLOK-UHFFFAOYSA-N 0.000 abstract 1
- DYTTXNQQICAXDN-UHFFFAOYSA-N 9h-fluorene-1,2-dicarbonitrile Chemical class C1=CC=C2C3=CC=C(C#N)C(C#N)=C3CC2=C1 DYTTXNQQICAXDN-UHFFFAOYSA-N 0.000 abstract 1
- ACQBHUKTPLFEOO-UHFFFAOYSA-N 9h-fluorene-1,7-dicarboxylic acid Chemical compound C1=CC=C(C(O)=O)C2=C1C1=CC=C(C(=O)O)C=C1C2 ACQBHUKTPLFEOO-UHFFFAOYSA-N 0.000 abstract 1
- RRLKPKUPGAXIQP-UHFFFAOYSA-N 9h-fluorene-2,5-diamine Chemical compound C1=CC(N)=C2C3=CC=C(N)C=C3CC2=C1 RRLKPKUPGAXIQP-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- 241000709664 Picornaviridae Species 0.000 abstract 1
- 206010046865 Vaccinia virus infection Diseases 0.000 abstract 1
- OQCDKGPJPMOXAL-UHFFFAOYSA-M [Cl-].[Mg+]CCCN1CCCCC1 Chemical compound [Cl-].[Mg+]CCCN1CCCCC1 OQCDKGPJPMOXAL-UHFFFAOYSA-M 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 230000000840 anti-viral effect Effects 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 abstract 1
- 150000004795 grignard reagents Chemical class 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 208000037797 influenza A Diseases 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
- 235000010288 sodium nitrite Nutrition 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 abstract 1
- 230000000699 topical effect Effects 0.000 abstract 1
- 241001529453 unidentified herpesvirus Species 0.000 abstract 1
- 208000007089 vaccinia Diseases 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/104—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/108—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/80—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen
- C07C49/813—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
- C07D211/14—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2346870A | 1970-03-27 | 1970-03-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1286775A true GB1286775A (en) | 1972-08-23 |
Family
ID=21815282
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB24584/71A Expired GB1286775A (en) | 1970-03-27 | 1971-04-19 | Bis-basic ketones of fluorene and fluorenone |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4064347A (enExample) |
| JP (1) | JPS5429488B1 (enExample) |
| AT (1) | AT304515B (enExample) |
| BE (1) | BE764870A (enExample) |
| CA (1) | CA959488A (enExample) |
| CH (2) | CH569694A5 (enExample) |
| CS (1) | CS179369B2 (enExample) |
| DE (1) | DE2114461A1 (enExample) |
| ES (1) | ES389604A1 (enExample) |
| FR (1) | FR2085747B1 (enExample) |
| GB (1) | GB1286775A (enExample) |
| HU (1) | HU162836B (enExample) |
| IE (1) | IE35023B1 (enExample) |
| IL (1) | IL36423A (enExample) |
| NL (1) | NL7104096A (enExample) |
| NO (1) | NO130513C (enExample) |
| PH (1) | PH9308A (enExample) |
| SE (1) | SE374540B (enExample) |
| ZA (1) | ZA711333B (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3859286A (en) * | 1970-12-11 | 1975-01-07 | Richardson Merrell Inc | Bis-basic ketones of xanthene and xanthen-9-one |
| US3983124A (en) * | 1972-12-21 | 1976-09-28 | Richardson-Merrell Inc. | Fluorene compounds |
| US4108896A (en) * | 1972-12-21 | 1978-08-22 | Richardson-Merrell Inc. | Anthracene derivatives |
| US4048230A (en) * | 1972-12-21 | 1977-09-13 | Richardson-Merrell Inc. | Aminoacetyl-acenaphthenes |
| US4461899A (en) * | 1982-05-24 | 1984-07-24 | Diamond Shamrock Chemicals Company | Fluorenecarboxylic acid derivatives |
| US6004959A (en) * | 1996-05-30 | 1999-12-21 | Hoechst Marion Roussel, Inc. | Alkyloxyamino substituted fluorenones and their use as protein kinase-C inhibitors |
| WO2005105772A1 (de) | 2004-04-14 | 2005-11-10 | Merck Patent Gmbh | Dibenzofuran-, dibenzothiophen- und fluorenderivate |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB286688A (en) | 1927-03-09 | 1929-05-16 | Schering Kahlbaum Ag | Process for the manufacture of new di-halogen-acylated diphenylethers and of highly active therapeutic substances therefrom |
| US2840558A (en) * | 1954-06-30 | 1958-06-24 | Shell Dev | Mannich bases of aromatic polyketones |
| US2783216A (en) * | 1954-06-30 | 1957-02-26 | Shell Dev | Resinous products from mannich bases of aromatic polyketones with hydrogen sulfide andor polythiols |
| NL132583C (enExample) * | 1960-11-09 | 1971-10-15 | ||
| US3083201A (en) * | 1961-02-13 | 1963-03-26 | Smith Kline French Lab | Glyoxal derivatives of dibenzofuran and dibenzothiophene |
| US3251733A (en) * | 1961-06-07 | 1966-05-17 | Geigy Chem Corp | Antimicrobic compositions and process for protection of organic materials therewith |
| US3576865A (en) * | 1968-10-11 | 1971-04-27 | Richardson Merrell Inc | Fluorenone-,fluorenol-,and fluorenebis-basic carboxamides |
-
1971
- 1971-03-02 ZA ZA711333A patent/ZA711333B/xx unknown
- 1971-03-12 CA CA107,591A patent/CA959488A/en not_active Expired
- 1971-03-16 IL IL36423A patent/IL36423A/xx unknown
- 1971-03-18 HU HUME1343A patent/HU162836B/hu unknown
- 1971-03-18 IE IE342/71A patent/IE35023B1/xx unknown
- 1971-03-19 PH PH12305*UA patent/PH9308A/en unknown
- 1971-03-22 AT AT245171A patent/AT304515B/de not_active IP Right Cessation
- 1971-03-23 JP JP1622271A patent/JPS5429488B1/ja active Pending
- 1971-03-24 CS CS7100002147A patent/CS179369B2/cs unknown
- 1971-03-24 CH CH277675A patent/CH569694A5/xx not_active IP Right Cessation
- 1971-03-24 CH CH427971A patent/CH564518A5/xx not_active IP Right Cessation
- 1971-03-25 FR FR7110659A patent/FR2085747B1/fr not_active Expired
- 1971-03-25 DE DE19712114461 patent/DE2114461A1/de not_active Withdrawn
- 1971-03-25 SE SE7103925A patent/SE374540B/xx unknown
- 1971-03-26 NO NO1144/71A patent/NO130513C/no unknown
- 1971-03-26 NL NL7104096A patent/NL7104096A/xx unknown
- 1971-03-26 ES ES389604A patent/ES389604A1/es not_active Expired
- 1971-03-26 BE BE764870A patent/BE764870A/xx not_active IP Right Cessation
- 1971-04-19 GB GB24584/71A patent/GB1286775A/en not_active Expired
-
1973
- 1973-02-02 US US05/328,912 patent/US4064347A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE2114461A1 (de) | 1971-10-14 |
| PH9308A (en) | 1975-08-18 |
| IE35023B1 (en) | 1975-10-15 |
| NO130513C (enExample) | 1974-12-27 |
| ZA711333B (en) | 1971-11-24 |
| BE764870A (fr) | 1971-08-16 |
| ES389604A1 (es) | 1973-06-16 |
| FR2085747B1 (enExample) | 1975-08-01 |
| IE35023L (en) | 1971-09-27 |
| IL36423A0 (en) | 1971-05-26 |
| CS179369B2 (en) | 1977-10-31 |
| SE374540B (enExample) | 1975-03-10 |
| CH564518A5 (enExample) | 1975-07-31 |
| FR2085747A1 (enExample) | 1971-12-31 |
| NL7104096A (enExample) | 1971-09-29 |
| CH569694A5 (enExample) | 1975-11-28 |
| CA959488A (en) | 1974-12-17 |
| HU162836B (enExample) | 1973-04-28 |
| JPS5429488B1 (enExample) | 1979-09-25 |
| NO130513B (enExample) | 1974-09-16 |
| AT304515B (de) | 1973-01-10 |
| IL36423A (en) | 1974-05-16 |
| US4064347A (en) | 1977-12-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2170733A1 (es) | Metodo para preparar citalopram purificado | |
| GB1476087A (en) | 5-aryl-1,2,3,4-tetrahydro-y-carbolines | |
| DK291685D0 (da) | Topisk behandling og praeparat | |
| GB2074158A (en) | Quinone compounds their production and use | |
| GB1514870A (en) | Imidazolyloxime ethers having antimycotic and bactericidal activity | |
| ES406081A1 (es) | Procedimiento de preparacion de nuevos derivados del acido butirico. | |
| IE42130L (en) | 2-phenyliminoimidazolidines | |
| Bougeois et al. | Total stereospecificity in free radical intramolecular addition: Cyclisation of cis and trans 1-methyl 4-hexenyl N-chloroamines by means of metallic salts | |
| IE35023B1 (en) | Bis-basic ketones of fluorene and fluorenone | |
| GB1228615A (enExample) | ||
| GB2099424A (en) | Isoprenylamine derivatives | |
| Duffield et al. | Mass spectrometry in structural and stereochemical problems. CCXXXVII—Electron‐impact‐induced hydrogen losses and migrations in some aromatic amides | |
| GB1416415A (en) | Biphenyl compounds and their use as light protective agents | |
| JPS5754126A (en) | Novel preparation of olefin compound | |
| IE35166B1 (en) | Bis-basic ketones of fluoranthene | |
| GB1416928A (en) | Anthracene derivatives | |
| Sugimoto et al. | Studies on the Synthetic Analgesics. XVII. Syntheses of 2-(N-tert-Aminoalkylacylamino) thiophene | |
| Giordano et al. | Electron-transfer processes: New synthesis of γ-lactones by peroxydisulfate oxidation of isopropylbenzenes and aliphatic carboxylic acids | |
| GB1434714A (en) | 3-amino-prop-1-enes methods for their preparation | |
| GB1420377A (en) | Bis basic alkoxy tricyclic compounds | |
| CN121159580A (zh) | 一种芳基偕二硼化合物或烷基偕二硼化合物的合成方法 | |
| YAMATO et al. | Synthesis and antiulcer activity of (isochroman-1-yl) alkylamines. I | |
| GB1420376A (en) | Substituted 9,10-dihydroanthracenes | |
| JPS5583779A (en) | Preparation of (3-methyl-2-thienyl)benzene derivative | |
| GB1271571A (en) | Basic monoazo dyes, their production and use |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |