AT377522B - Verfahren zur herstellung von furo-(3,4-c)pyridinderivaten - Google Patents
Verfahren zur herstellung von furo-(3,4-c)pyridinderivatenInfo
- Publication number
- AT377522B AT377522B AT0016082A AT16082A AT377522B AT 377522 B AT377522 B AT 377522B AT 0016082 A AT0016082 A AT 0016082A AT 16082 A AT16082 A AT 16082A AT 377522 B AT377522 B AT 377522B
- Authority
- AT
- Austria
- Prior art keywords
- furo
- production
- pyridine derivatives
- pyridine
- derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D499/21—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D499/28—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with modified 2-carboxyl group
- C07D499/32—Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Cephalosporin Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/039,539 US4244951A (en) | 1979-05-16 | 1979-05-16 | Bis-esters of methanediol with penicillins and penicillanic acid 1,1-dioxide |
Publications (2)
Publication Number | Publication Date |
---|---|
ATA16082A ATA16082A (de) | 1984-08-15 |
AT377522B true AT377522B (de) | 1985-03-25 |
Family
ID=21906015
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT0258880A AT369373B (de) | 1979-05-16 | 1980-05-14 | Verfahren zur herstellung von neuen penicillinderivaten |
AT0016082A AT377522B (de) | 1979-05-16 | 1982-01-18 | Verfahren zur herstellung von furo-(3,4-c)pyridinderivaten |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT0258880A AT369373B (de) | 1979-05-16 | 1980-05-14 | Verfahren zur herstellung von neuen penicillinderivaten |
Country Status (44)
Country | Link |
---|---|
US (1) | US4244951A (de) |
JP (1) | JPS55157589A (de) |
KR (1) | KR840000105B1 (de) |
AR (1) | AR226062A1 (de) |
AT (2) | AT369373B (de) |
AU (1) | AU520066B2 (de) |
BE (1) | BE883299A (de) |
BG (1) | BG35467A3 (de) |
CA (1) | CA1200545A (de) |
CH (1) | CH646177A5 (de) |
CS (1) | CS276964B6 (de) |
DD (1) | DD150898A5 (de) |
DE (2) | DE3018590A1 (de) |
DK (1) | DK159786C (de) |
EC (1) | ECSP941080A (de) |
EG (1) | EG15129A (de) |
ES (1) | ES491534A0 (de) |
FI (1) | FI71742C (de) |
FR (2) | FR2456745A1 (de) |
GB (2) | GB2051057B (de) |
GR (1) | GR68468B (de) |
GT (1) | GT198063473A (de) |
HK (2) | HK66787A (de) |
HU (1) | HU184754B (de) |
IE (1) | IE49892B1 (de) |
IL (1) | IL60074A (de) |
IN (1) | IN154371B (de) |
IT (1) | IT1131187B (de) |
KE (2) | KE3460A (de) |
LU (1) | LU82452A1 (de) |
MX (1) | MX6717E (de) |
MY (2) | MY8500322A (de) |
NL (1) | NL8002793A (de) |
NO (3) | NO801415L (de) |
NZ (1) | NZ193713A (de) |
PH (3) | PH16554A (de) |
PL (2) | PL127434B1 (de) |
PT (1) | PT71248A (de) |
RO (2) | RO84151B (de) |
SE (1) | SE449749B (de) |
SG (1) | SG56284G (de) |
SU (2) | SU1122226A3 (de) |
YU (1) | YU41925B (de) |
ZA (1) | ZA801885B (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT397093B (de) * | 1988-04-06 | 1994-01-25 | Sod Conseils Rech Applic | Stereospezifisches verfahren für die herstellung von enantiomeren des 3-substituierten furo (3,4-c) pyridins, so erhaltene enantiomere oder mischungen davon sowie diese enthaltene therapeutische mittel |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE49881B1 (en) * | 1979-02-13 | 1986-01-08 | Leo Pharm Prod Ltd | B-lactam intermediates |
US4309347A (en) * | 1979-05-16 | 1982-01-05 | Pfizer Inc. | Penicillanoyloxymethyl penicillanate 1,1,1',1'-tetraoxide |
DE3051044C2 (de) * | 1979-06-19 | 1989-03-30 | Leo Pharmaceutical Products Ltd. A/S (Loevens Kemiske Fabrik Produktionsaktieselskab), Ballerup, Dk | |
US4364957A (en) * | 1979-09-26 | 1982-12-21 | Pfizer Inc. | Bis-esters of alkanediols as antibacterial agents |
US4342768A (en) * | 1979-10-22 | 1982-08-03 | Pfizer Inc. | Bis-esters of 1,1-alkanediols with 6-beta-hydroxymethylpenicillanic acid 1,1-dioxide and beta-lactam antibiotics |
IL61880A (en) * | 1980-01-21 | 1984-11-30 | Bristol Myers Co | 2beta-chloromethyl-2alpha-methylpenam-3alpha-carboxylic acid sulfone derivatives,their preparation and pharmaceutical compositions containing them |
US4488994A (en) * | 1980-09-08 | 1984-12-18 | Pfizer Inc. | Bis-esters of methanediol with penicillins and penicillanic acid 1,1-dioxide |
IE51516B1 (en) * | 1980-10-06 | 1987-01-07 | Leo Pharm Prod Ltd | 1,1-dioxapenicillanoyloxymethyl 6-(d-alpha-amino-alpha-phenylacetamido)penicillanate napsylate |
IL64009A (en) * | 1980-10-31 | 1984-09-30 | Rech Applications Therap | Crystalline 1,1-dioxopenicillanoyloxymethyl 6-(d-alpha-amino-alpha-phenylacetamido)penicillanate tosylate hydrates,their production and pharmaceutical compositions containing them |
US4474698A (en) * | 1980-12-11 | 1984-10-02 | Pfizer Inc. | Process for preparing esters of penicillanic acid sulfone |
US4323499A (en) * | 1981-01-05 | 1982-04-06 | Pfizer Inc. | 6-(2-Aryl-2-(1,1-dioxopenicillanoyloxy-methoxycarbonyl)acetamido penicillanic acids |
US4478748A (en) * | 1981-02-20 | 1984-10-23 | Pfizer Inc. | Bis-esters of alkanediols |
IN157669B (de) * | 1981-03-23 | 1986-05-17 | Pfizer | |
US4321196A (en) * | 1981-03-23 | 1982-03-23 | Pfizer Inc. | Bis-esters of methanediol with acetonides of ampicillin or amoxicillin and penicillanic acid 1,1-dioxide |
US4393001A (en) * | 1981-03-23 | 1983-07-12 | Pfizer Inc. | Intermediates for production of 1,1-dioxopenicillanoyloxymethyl 6-(2-amino-2-phenylacetamido)penicillanates |
US4376076A (en) * | 1981-03-23 | 1983-03-08 | Pfizer Inc. | Bis-esters of 1,1-alkanediols with 6-beta-hydroxymethylpenicillanic acid 1,1-dioxide |
US4381263A (en) * | 1981-03-23 | 1983-04-26 | Pfizer Inc. | Process for the preparation of penicillanic acid esters |
US4582829A (en) * | 1981-09-09 | 1986-04-15 | Pfizer Inc. | Antibacterial 6'-(2-amino-2-[4-acyloxyphenyl]acetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide compounds |
US4540687A (en) * | 1981-09-09 | 1985-09-10 | Pfizer Inc. | Antibacterial 6'-(2-amino-2-[4-acyloxyphenyl]acetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide compounds |
ZA826687B (en) * | 1981-09-14 | 1983-07-27 | Pfizer | Beta-lactamase inhibiting 2-beta-substituted-2-alpha-methyl 5(r)penam-3-alpha-carboxylic acid 1,1-dioxides and intermediates therefor |
US4351840A (en) * | 1981-09-18 | 1982-09-28 | Pfizer Inc. | Antibacterial esters of resorcinol with ampicillin and penicillanic acid 1,1-dioxide derivatives |
US4359472A (en) * | 1981-12-22 | 1982-11-16 | Pfizer Inc. | Bis-hydroxymethyl carbonate bridged antibacterial agents |
US4457924A (en) * | 1981-12-22 | 1984-07-03 | Pfizer, Inc. | 1,1-Alkanediol dicarboxylate linked antibacterial agents |
US4452796A (en) * | 1982-06-14 | 1984-06-05 | Pfizer Inc. | 6-Aminoalkylpenicillanic acid 1,1-dioxides as beta-lactamase inhibitors |
EP0084730A1 (de) * | 1982-01-22 | 1983-08-03 | Beecham Group Plc | Ester von Penicillinderivaten mit Beta-Lactamase-Inhibitoren, ihre Herstellung und ihre Verwendung |
US4444686A (en) * | 1982-01-25 | 1984-04-24 | Pfizer Inc. | Crystalline penicillin ester intermediate |
US4432987A (en) * | 1982-04-23 | 1984-02-21 | Pfizer Inc. | Crystalline benzenesulfonate salts of sultamicillin |
US4377590A (en) * | 1982-05-10 | 1983-03-22 | Pfizer Inc. | Derivatives of ampicillin and amoxicillin with beta-lactamase inhibitors |
US4428935A (en) | 1982-05-24 | 1984-01-31 | Pfizer Inc. | Penicillanic acid dioxide prodrug |
US4375434A (en) * | 1982-06-21 | 1983-03-01 | Pfizer Inc. | Process for 6'-amino-penicillanoyloxymethyl penicillanate 1,1-dioxide |
US4530792A (en) * | 1982-11-01 | 1985-07-23 | Pfizer Inc. | Process and intermediates for preparation of 1,1-dioxopenicillanoyloxymethyl 6-beta-aminopenicillanate |
US4868297A (en) * | 1982-12-06 | 1989-09-19 | Pfizer Inc. | Process for preparing sultamicillin and analogs |
US4462934A (en) * | 1983-03-31 | 1984-07-31 | Pfizer Inc. | Bis-esters of dicarboxylic acids with amoxicillin and certain hydroxymethylpenicillanate 1,1-dioxides |
US4536393A (en) * | 1983-06-06 | 1985-08-20 | Pfizer Inc. | 6-(Aminomethyl)penicillanic acid 1,1-dioxide esters and intermediates therefor |
JPS60214792A (ja) * | 1984-04-06 | 1985-10-28 | Taiho Yakuhin Kogyo Kk | ペナム酸エステル誘導体 |
JPH01139584A (ja) * | 1987-11-25 | 1989-06-01 | Yoshitomi Pharmaceut Ind Ltd | ペニシラン酸化合物の製造法 |
GB8808701D0 (en) * | 1988-04-13 | 1988-05-18 | Erba Carlo Spa | Beta-lactam derivatives |
GB2231049A (en) * | 1989-04-14 | 1990-11-07 | Yoshitomi Pharmaceutical | Method for producing diester compounds |
KR910009271B1 (ko) * | 1989-06-20 | 1991-11-08 | 김영설 | 1,1-디옥소페닐실라노일 옥시메틸 D-6-[α-(메틸렌아미노)페닐-아세트아미도]-페니실라네이트와 그의 파라-톨루엔술폰산염 |
DE69103003T2 (de) * | 1990-04-13 | 1994-11-03 | Pfizer Inc., Groton, Conn. | Verfahren für sultamicillinzwischenprodukt. |
CN100384857C (zh) | 2003-11-28 | 2008-04-30 | 浙江永宁制药厂 | 耐β-内酰胺酶的头孢菌素酯化合物及其盐 |
IT202000031070A1 (it) | 2020-12-16 | 2022-06-16 | Paolo Bonomi | Procedimento di sintesi di derivati ammidici dell’acido 8-idrossi penicillanico |
CN115385934A (zh) * | 2022-10-26 | 2022-11-25 | 北京纳百生物科技有限公司 | 一种舒巴坦半抗原及其合成方法和应用 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE34948B1 (en) * | 1970-03-12 | 1975-10-01 | Leo Pharm Prod Ltd | New penicillin esters |
GB1303491A (de) * | 1970-03-24 | 1973-01-17 | ||
GB1335718A (en) * | 1971-05-05 | 1973-10-31 | Leo Pharm Prod Ltd | Penicillin esters salts thereof and methods for their preparation |
US3838152A (en) * | 1971-10-07 | 1974-09-24 | American Home Prod | Poly alpha-amino penicillins |
DE2460477A1 (de) * | 1973-12-26 | 1975-07-10 | Yamanouchi Pharma Co Ltd | Verbessertes verfahren zur herstellung von 6-alkoxy-substituierten penicillinen |
GB1467604A (en) * | 1974-06-27 | 1977-03-16 | Toyama Chemical Co Ltd | Bis-type penicillins and process for producing the same |
GB1578128A (en) * | 1976-03-30 | 1980-11-05 | Leo Pharm Prod Ltd | Amidinopenicillanoyloxyalkyl amoxycillinates |
IN149747B (de) * | 1977-06-07 | 1982-04-03 | Pfizer | |
KR830001903B1 (ko) * | 1979-02-13 | 1983-09-19 | 레오 파마슈티칼 프로덕츠 리미티드 | 페니실란산유도체의 제조방법 |
IE49881B1 (en) | 1979-02-13 | 1986-01-08 | Leo Pharm Prod Ltd | B-lactam intermediates |
-
1979
- 1979-05-16 US US06/039,539 patent/US4244951A/en not_active Expired - Lifetime
-
1980
- 1980-03-31 ZA ZA00801885A patent/ZA801885B/xx unknown
- 1980-04-22 IN IN290/DEL/80A patent/IN154371B/en unknown
- 1980-05-08 CS CS803252A patent/CS276964B6/cs not_active IP Right Cessation
- 1980-05-08 HU HU801136A patent/HU184754B/hu unknown
- 1980-05-08 SU SU802921352A patent/SU1122226A3/ru active
- 1980-05-09 RO RO108682A patent/RO84151B/ro unknown
- 1980-05-09 RO RO80101076A patent/RO80220A/ro unknown
- 1980-05-09 BG BG047702A patent/BG35467A3/xx unknown
- 1980-05-13 NO NO801415A patent/NO801415L/no unknown
- 1980-05-13 SE SE8003603A patent/SE449749B/sv not_active IP Right Cessation
- 1980-05-13 FI FI801546A patent/FI71742C/fi not_active IP Right Cessation
- 1980-05-13 CA CA000351802A patent/CA1200545A/en not_active Expired
- 1980-05-14 FR FR8010886A patent/FR2456745A1/fr active Granted
- 1980-05-14 DK DK211880A patent/DK159786C/da active
- 1980-05-14 PL PL1980224225A patent/PL127434B1/pl unknown
- 1980-05-14 NZ NZ193713A patent/NZ193713A/en unknown
- 1980-05-14 GR GR61944A patent/GR68468B/el unknown
- 1980-05-14 LU LU82452A patent/LU82452A1/fr unknown
- 1980-05-14 AR AR281014A patent/AR226062A1/es active
- 1980-05-14 IL IL60074A patent/IL60074A/xx unknown
- 1980-05-14 PL PL1980230846A patent/PL127283B1/pl unknown
- 1980-05-14 BE BE0/200615A patent/BE883299A/fr not_active IP Right Cessation
- 1980-05-14 AT AT0258880A patent/AT369373B/de active
- 1980-05-14 NL NL8002793A patent/NL8002793A/nl not_active Application Discontinuation
- 1980-05-14 DE DE19803018590 patent/DE3018590A1/de not_active Withdrawn
- 1980-05-14 CH CH380680A patent/CH646177A5/de not_active IP Right Cessation
- 1980-05-14 MX MX808811U patent/MX6717E/es unknown
- 1980-05-14 PH PH24029A patent/PH16554A/en unknown
- 1980-05-14 ES ES491534A patent/ES491534A0/es active Granted
- 1980-05-14 DE DE19803050440 patent/DE3050440A1/de active Pending
- 1980-05-14 AU AU58396/80A patent/AU520066B2/en not_active Expired
- 1980-05-15 GB GB8016136A patent/GB2051057B/en not_active Expired
- 1980-05-15 KR KR1019800001917A patent/KR840000105B1/ko active
- 1980-05-15 JP JP6465480A patent/JPS55157589A/ja active Granted
- 1980-05-15 PT PT71248A patent/PT71248A/pt unknown
- 1980-05-15 IE IE1007/80A patent/IE49892B1/en not_active IP Right Cessation
- 1980-05-15 IT IT22097/80A patent/IT1131187B/it active
- 1980-05-15 YU YU1303/80A patent/YU41925B/xx unknown
- 1980-05-15 GB GB8127095A patent/GB2081269B/en not_active Expired
- 1980-05-16 GT GT198063473A patent/GT198063473A/es unknown
- 1980-05-16 DD DD80221170A patent/DD150898A5/de unknown
- 1980-05-17 EG EG308/80A patent/EG15129A/xx active
-
1981
- 1981-02-20 FR FR8103436A patent/FR2477154A1/fr active Granted
- 1981-04-27 SU SU813274747A patent/SU1122228A3/ru active
- 1981-04-27 PH PH25556A patent/PH15539A/en unknown
- 1981-04-27 PH PH25555A patent/PH15706A/en unknown
-
1982
- 1982-01-18 AT AT0016082A patent/AT377522B/de not_active IP Right Cessation
-
1983
- 1983-03-23 NO NO831026A patent/NO831026L/no unknown
- 1983-03-23 NO NO831025A patent/NO831025L/no unknown
-
1984
- 1984-08-13 SG SG562/84A patent/SG56284G/en unknown
- 1984-09-24 KE KE3460A patent/KE3460A/xx unknown
- 1984-09-24 KE KE3457A patent/KE3457A/xx unknown
-
1985
- 1985-12-30 MY MY322/85A patent/MY8500322A/xx unknown
- 1985-12-30 MY MY324/85A patent/MY8500324A/xx unknown
-
1987
- 1987-09-17 HK HK667/87A patent/HK66787A/xx not_active IP Right Cessation
- 1987-09-17 HK HK669/87A patent/HK66987A/xx not_active IP Right Cessation
-
1994
- 1994-05-05 EC EC1994001080A patent/ECSP941080A/es unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT397093B (de) * | 1988-04-06 | 1994-01-25 | Sod Conseils Rech Applic | Stereospezifisches verfahren für die herstellung von enantiomeren des 3-substituierten furo (3,4-c) pyridins, so erhaltene enantiomere oder mischungen davon sowie diese enthaltene therapeutische mittel |
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