NO310557B1 - Fremgangsmåte ved fremstilling av Ginkgolid B fra Ginkgolid C - Google Patents
Fremgangsmåte ved fremstilling av Ginkgolid B fra Ginkgolid C Download PDFInfo
- Publication number
- NO310557B1 NO310557B1 NO19951524A NO951524A NO310557B1 NO 310557 B1 NO310557 B1 NO 310557B1 NO 19951524 A NO19951524 A NO 19951524A NO 951524 A NO951524 A NO 951524A NO 310557 B1 NO310557 B1 NO 310557B1
- Authority
- NO
- Norway
- Prior art keywords
- ginkgolide
- borohydride
- group
- reaction
- carried out
- Prior art date
Links
- AMOGMTLMADGEOQ-DPFZUGDXSA-N ginkgolide C Natural products O=C1[C@@H](C)[C@]2(O)[C@H]([C@H](O)[C@@]34[C@H]5[C@H](O)[C@@H](C(C)(C)C)[C@]63[C@H](O)C(=O)O[C@H]6O[C@@]24C(=O)O5)O1 AMOGMTLMADGEOQ-DPFZUGDXSA-N 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 23
- SQOJOAFXDQDRGF-NNGCZKEZSA-N ginkgolide B Chemical compound C12([C@H](C(C)(C)C)C[C@H]3OC4=O)[C@@H](O)C(=O)O[C@H]1O[C@]14C23[C@@H](O)[C@@H]2OC(=O)[C@@H](C)[C@]12O SQOJOAFXDQDRGF-NNGCZKEZSA-N 0.000 title 1
- SQOJOAFXDQDRGF-MMQTXUMRSA-N ginkgolide-b Chemical compound O[C@H]([C@]12[C@H](C(C)(C)C)C[C@H]3OC4=O)C(=O)O[C@H]2O[C@]24[C@@]13[C@@H](O)[C@@H]1OC(=O)[C@@H](C)[C@]21O SQOJOAFXDQDRGF-MMQTXUMRSA-N 0.000 claims abstract description 24
- SQOJOAFXDQDRGF-WJHVHIKBSA-N ginkgolide B Natural products O=C1[C@@H](C)[C@@]2(O)[C@@H]([C@H](O)[C@]34[C@@H]5OC(=O)[C@]23O[C@H]2OC(=O)[C@H](O)[C@@]42[C@H](C(C)(C)C)C5)O1 SQOJOAFXDQDRGF-WJHVHIKBSA-N 0.000 claims abstract description 23
- 239000000010 aprotic solvent Substances 0.000 claims abstract description 4
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 3
- AMOGMTLMADGEOQ-FNZROXQESA-N Ginkgolide C Chemical compound O([C@H]1O2)C(=O)[C@H](O)C31[C@]14[C@@H](O)[C@@H]5OC(=O)[C@@H](C)[C@]5(O)[C@@]12C(=O)O[C@@H]4[C@@H](O)[C@H]3C(C)(C)C AMOGMTLMADGEOQ-FNZROXQESA-N 0.000 claims description 24
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 22
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 claims description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical group CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical group CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims description 4
- 125000001894 2,4,6-trinitrophenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O 0.000 claims description 2
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 2
- 150000003863 ammonium salts Chemical class 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 125000005207 tetraalkylammonium group Chemical group 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229930184727 ginkgolide Natural products 0.000 abstract description 8
- WJKHJLXJJJATHN-UHFFFAOYSA-N triflic anhydride Chemical compound FC(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F WJKHJLXJJJATHN-UHFFFAOYSA-N 0.000 description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- -1 diterpene lactones Chemical class 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000008100 Ginkgo biloba Nutrition 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MLSGSTVEFFOWLW-UHFFFAOYSA-N (2,4,6-trinitrophenyl)sulfonyl 2,4,6-trinitrobenzenesulfonate Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1S(=O)(=O)OS(=O)(=O)C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O MLSGSTVEFFOWLW-UHFFFAOYSA-N 0.000 description 1
- VPAHTUQECJIGCK-UHFFFAOYSA-N (2-methylphenyl)sulfonyl 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S(=O)(=O)OS(=O)(=O)C1=CC=CC=C1C VPAHTUQECJIGCK-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 235000011201 Ginkgo Nutrition 0.000 description 1
- 241000218628 Ginkgo Species 0.000 description 1
- 244000194101 Ginkgo biloba Species 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- MLWPJXZKQOPTKZ-UHFFFAOYSA-N benzenesulfonyl benzenesulfonate Chemical compound C=1C=CC=CC=1S(=O)(=O)OS(=O)(=O)C1=CC=CC=C1 MLWPJXZKQOPTKZ-UHFFFAOYSA-N 0.000 description 1
- QDHFHIQKOVNCNC-UHFFFAOYSA-N butane-1-sulfonic acid Chemical compound CCCCS(O)(=O)=O QDHFHIQKOVNCNC-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000006392 deoxygenation reaction Methods 0.000 description 1
- 229930004069 diterpene Natural products 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- IZDROVVXIHRYMH-UHFFFAOYSA-N methanesulfonic anhydride Chemical compound CS(=O)(=O)OS(C)(=O)=O IZDROVVXIHRYMH-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- SCHZCUMIENIQMY-UHFFFAOYSA-N tris(trimethylsilyl)silicon Chemical compound C[Si](C)(C)[Si]([Si](C)(C)C)[Si](C)(C)C SCHZCUMIENIQMY-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/22—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/01—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicines Containing Plant Substances (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9408044A GB9408044D0 (en) | 1994-04-22 | 1994-04-22 | Conversion of ginkgolide c to ginkgolide b |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO951524D0 NO951524D0 (no) | 1995-04-21 |
| NO951524L NO951524L (no) | 1995-10-23 |
| NO310557B1 true NO310557B1 (no) | 2001-07-23 |
Family
ID=10753985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19951524A NO310557B1 (no) | 1994-04-22 | 1995-04-21 | Fremgangsmåte ved fremstilling av Ginkgolid B fra Ginkgolid C |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US5599950A (ko) |
| EP (1) | EP0680968B1 (ko) |
| JP (1) | JP2992575B2 (ko) |
| KR (1) | KR950032203A (ko) |
| AT (1) | ATE189817T1 (ko) |
| AU (1) | AU684338B2 (ko) |
| CA (1) | CA2147423C (ko) |
| DE (1) | DE69515077T2 (ko) |
| DK (1) | DK0680968T3 (ko) |
| DZ (1) | DZ1874A1 (ko) |
| ES (1) | ES2144585T3 (ko) |
| FI (1) | FI109907B (ko) |
| FR (1) | FR2719046B1 (ko) |
| GB (2) | GB9408044D0 (ko) |
| IE (1) | IE80950B1 (ko) |
| MY (1) | MY113056A (ko) |
| NO (1) | NO310557B1 (ko) |
| NZ (1) | NZ270925A (ko) |
| OA (1) | OA10145A (ko) |
| RU (1) | RU2145326C1 (ko) |
| TN (1) | TNSN95041A1 (ko) |
| TW (1) | TW300897B (ko) |
| ZA (1) | ZA952986B (ko) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5981902A (en) * | 1994-12-15 | 1999-11-09 | Mitsubishi Chemical Corporation | Texturing apparatus for magnetic recording medium and magnetic recording medium process thereby |
| WO1998016531A1 (en) * | 1996-10-16 | 1998-04-23 | Merck & Co., Inc. | Triterpene derivatives with immunosupressant activity |
| WO1998016532A1 (en) * | 1996-10-16 | 1998-04-23 | Merck & Co., Inc. | Triterpene derivatives with immunosuppressant activity |
| US6100293A (en) * | 1997-10-17 | 2000-08-08 | Merck & Co., Inc. | Tetracyclic triterpene derivatives with immunosuppressant activity |
| US6083980A (en) * | 1997-10-17 | 2000-07-04 | Merck & Co., Inc. | Furanyl, tetracyclic triterpene derivatives with immunosuppressant activity |
| US6022890A (en) * | 1997-11-14 | 2000-02-08 | Merck & Co., Inc. | Immunosuppressant tetracyclic triterpenes |
| US6030621A (en) | 1998-03-19 | 2000-02-29 | De Long; Xie | Ginkgo biloba composition, method to prepare the same and uses thereof |
| US6051590A (en) * | 1999-05-13 | 2000-04-18 | Merck & Co., Inc. | Immunosuppressant tricyclic compounds |
| US6946283B2 (en) * | 2001-01-05 | 2005-09-20 | William Marsh Rice University | Ginkgo biloba levopimaradiene synthase |
| US7238514B2 (en) * | 2001-01-05 | 2007-07-03 | William Marsh Rice University | Diterpene-producing unicellular organism |
| FR2823116B1 (fr) * | 2001-04-10 | 2004-11-19 | Sod Conseils Rech Applic | Procede de preparation d'une extrait de feuilles de ginkgo biloba hautement enrichi en principes actifs |
| US6693091B2 (en) | 2002-03-29 | 2004-02-17 | The Trustees Of Columbia University In The City Of New York | Analogs of terpene trilactones from Ginkgo biloba for bioorganic and imaging studies |
| AU2003243158A1 (en) * | 2002-03-29 | 2003-10-13 | The Trustees Of Columbia University In The City Of New York | Analogs of terpene trilactones from ginkgo biloba and related compounds and uses thereof |
| US7429670B2 (en) * | 2003-08-27 | 2008-09-30 | The Trustees Of Columbia University In The City Of New York | Synthesis of derivatives of ginkgolide C |
| US7763741B2 (en) | 2003-11-12 | 2010-07-27 | The Trustees Of Columbia University In The City Of New York | Separation of ginkgolides and bilobalide from G. biloba |
| WO2005092324A1 (en) * | 2004-03-19 | 2005-10-06 | The Trustees Of Columbia University In The City Of New York | Ginkgolide compounds, compositions, extracts, and uses thereof |
| US20080306145A1 (en) * | 2004-11-23 | 2008-12-11 | The Trustees Of Columbia University In The City Of New York | Preparation Of Ginkgolide And F-Seco-Ginkgolide Lactols |
| WO2007002410A2 (en) * | 2005-06-22 | 2007-01-04 | The Trustees Of Columbia University In The City Of New York | Core-modified terpene trilactones from ginkgo biloba extract and biological evaluation thereof |
| CN102382121A (zh) * | 2010-09-02 | 2012-03-21 | 秦引林 | 银杏内酯衍生物及其在制药中的应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8418424D0 (en) * | 1984-07-19 | 1984-08-22 | Scras | Inhibition of platelets aggregation |
| KR940002795B1 (ko) * | 1989-06-16 | 1994-04-02 | 주식회사 선경인더스트리 | 은행잎에서 징코라이드를 분리 및 정제하는 방법 |
| GB9107425D0 (en) * | 1991-04-09 | 1991-05-22 | Scras | Preparation of ginkgolide b |
-
1994
- 1994-04-22 GB GB9408044A patent/GB9408044D0/en active Pending
- 1994-08-04 US US08/287,632 patent/US5599950A/en not_active Expired - Lifetime
-
1995
- 1995-04-10 IE IE950265A patent/IE80950B1/en not_active IP Right Cessation
- 1995-04-10 TW TW084103406A patent/TW300897B/zh active
- 1995-04-11 ZA ZA952986A patent/ZA952986B/xx unknown
- 1995-04-12 NZ NZ270925A patent/NZ270925A/en not_active IP Right Cessation
- 1995-04-18 GB GB9507801A patent/GB2288599B/en not_active Expired - Fee Related
- 1995-04-19 DZ DZ950042A patent/DZ1874A1/fr active
- 1995-04-20 AT AT95400876T patent/ATE189817T1/de active
- 1995-04-20 CA CA002147423A patent/CA2147423C/en not_active Expired - Fee Related
- 1995-04-20 ES ES95400876T patent/ES2144585T3/es not_active Expired - Lifetime
- 1995-04-20 FR FR9504709A patent/FR2719046B1/fr not_active Expired - Fee Related
- 1995-04-20 EP EP95400876A patent/EP0680968B1/fr not_active Expired - Lifetime
- 1995-04-20 MY MYPI95001032A patent/MY113056A/en unknown
- 1995-04-20 DK DK95400876T patent/DK0680968T3/da active
- 1995-04-20 AU AU16566/95A patent/AU684338B2/en not_active Ceased
- 1995-04-20 DE DE69515077T patent/DE69515077T2/de not_active Expired - Lifetime
- 1995-04-21 FI FI951903A patent/FI109907B/fi not_active IP Right Cessation
- 1995-04-21 JP JP7096757A patent/JP2992575B2/ja not_active Expired - Fee Related
- 1995-04-21 KR KR1019950009403A patent/KR950032203A/ko not_active Application Discontinuation
- 1995-04-21 TN TNTNSN95041A patent/TNSN95041A1/fr unknown
- 1995-04-21 OA OA60645A patent/OA10145A/fr unknown
- 1995-04-21 RU RU95106678A patent/RU2145326C1/ru not_active IP Right Cessation
- 1995-04-21 NO NO19951524A patent/NO310557B1/no unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO310557B1 (no) | Fremgangsmåte ved fremstilling av Ginkgolid B fra Ginkgolid C | |
| PL177730B1 (pl) | Pochodne galantaminy oraz kompozycja farmaceutyczna zawierająca pochodne galantaminy | |
| CA2118171C (en) | Galanthamine derivatives, a process for their preparation and their use as medicaments | |
| EP0541807A1 (en) | Novel benzopyran derivative | |
| US4228079A (en) | Dialkoxy monorden derivatives | |
| Bonesi et al. | On the synthesis and isolation of chlorocarbazoles obtained by chlorination of carbazoles | |
| NO130398B (ko) | ||
| CA1043348A (en) | Benzophenone derivatives and process for their production | |
| NO821954L (no) | Fremgangsmaate ved fremstilling av apovincaminsyreestere | |
| JPS634543B2 (ko) | ||
| CA1130806A (en) | 1,2,4-oxadiazole derivatives, their preparation and pharmaceutical use | |
| KR20000010893A (ko) | 마피아 포에티다(mappia foetida)에서 분리한캄토테신골격화합물 및 이들의 신규한 치료제 및 의약품기질로서의 용도 | |
| FR2653771A1 (fr) | Procede de preparation de l'azt (azido-3'-desoxy-3'-thymidine) et de composes apparentes. | |
| KR20060132910A (ko) | 스퐁고신의 합성 | |
| NO312593B1 (no) | Fremgangsmåte til fremstilling av et deoksyuridinderivat | |
| JPH03220194A (ja) | スタウロスポリンカルボン酸誘導体 | |
| CZ284321B6 (cs) | Způsob přípravy fysostigminkarbamátových derivátů z fysostigminu | |
| US6084108A (en) | Synthesis of 3-carbomethoxy-4,5-dimethylthiophene | |
| Esses‐Reiter et al. | Attempted synthesis of a tenidap isomer and formation of an unexpected stable water adduct | |
| CN113754681A (zh) | 一种具有双螺环结构五取代环戊烷的合成方法 | |
| DK151630B (da) | Analogifremgangsmaade til fremstilling af n-phthalidyl-5-fluoruracilderivater | |
| KR100218196B1 (ko) | 2-아미노티아졸 카르복사미드 유도체의 제조방법 | |
| CN116253697A (zh) | 一种二氯萘醌和甲胺类化合物为原料合成醌并噻唑类化合物的方法 | |
| US6333414B1 (en) | Process for the synthesis of trisubstituted oxazoles | |
| NO822864L (no) | Fremgangsmaate ved fremstilling av alkoxy-vincaminsyreestere og alkoxy-apovincaminsyreestere |