ATE3863T1 - Verfahren zur herstellung von 6,6-dimethyl-4hydroxy-3-oxabicyclo(3.1.0)-2-hexanon und seiner aether jeglicher stereoisomerer form. - Google Patents
Verfahren zur herstellung von 6,6-dimethyl-4hydroxy-3-oxabicyclo(3.1.0)-2-hexanon und seiner aether jeglicher stereoisomerer form.Info
- Publication number
- ATE3863T1 ATE3863T1 AT80401093T AT80401093T ATE3863T1 AT E3863 T1 ATE3863 T1 AT E3863T1 AT 80401093 T AT80401093 T AT 80401093T AT 80401093 T AT80401093 T AT 80401093T AT E3863 T1 ATE3863 T1 AT E3863T1
- Authority
- AT
- Austria
- Prior art keywords
- formula
- compound
- hydrogen
- reacting
- image
- Prior art date
Links
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title abstract 5
- QHAPONCMFJQXEN-UHFFFAOYSA-N 4-hydroxy-6,6-dimethyl-3-oxabicyclo[3.1.0]hexan-2-one Chemical compound O=C1OC(O)C2C1C2(C)C QHAPONCMFJQXEN-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- BWWAZRFAUNZGIS-UHFFFAOYSA-N CC(C)=[SH2] Chemical compound CC(C)=[SH2] BWWAZRFAUNZGIS-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/60—Two oxygen atoms, e.g. succinic anhydride
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Furan Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7919654A FR2472570A1 (fr) | 1979-07-31 | 1979-07-31 | Procede de preparation du (1,5) 6,6-dimethyl 4-hydroxy 3-oxa bicylo(3.1.0.)hexan-2-one et de ses ethers en position 4, sous toutes leurs formes stereoisomeres |
EP80401093A EP0023454B1 (fr) | 1979-07-31 | 1980-07-23 | Procédé de préparation de la 6,6-diméthyl-4-hydroxy-3-oxabicyclo(3.1.0)hexan-2-one et de ses éthers sous toutes leurs formes stéréoisomères |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE3863T1 true ATE3863T1 (de) | 1983-07-15 |
Family
ID=9228479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT80401093T ATE3863T1 (de) | 1979-07-31 | 1980-07-23 | Verfahren zur herstellung von 6,6-dimethyl-4hydroxy-3-oxabicyclo(3.1.0)-2-hexanon und seiner aether jeglicher stereoisomerer form. |
Country Status (9)
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3560714D1 (en) * | 1984-02-14 | 1987-11-05 | Sumitomo Chemical Co | Process for preparing optically active 4-hydroxy-2-cyclipentenones |
HU231350B1 (hu) * | 2019-12-18 | 2023-01-28 | CHINOIN Gyógyszer és Vegyészeti Termékek Gyára Zrt | Eljárás királis prosztaglandin-enol intermedier előállítására, és az eljárásban hasznos köztitermék vegyületek |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1072629B (de) * | 1960-01-07 | Unilever N. V., Rotterdam (Niederlande) | Verfahren zur Herstellung von Dihydrofuranonderivaten | |
US3907842A (en) * | 1974-04-01 | 1975-09-23 | Lilly Co Eli | Preparation of 6{60 {0 and 6{62 {0 carboxymethylsteroid conjugates |
FR2419932A2 (fr) * | 1978-03-17 | 1979-10-12 | Roussel Uclaf | Nouveaux esters d'acides cyclopropane carboxyliques comportant un substituant polyhalogene, procede de preparation et compositions insecticides les renfermant |
ZA7911B (en) * | 1978-01-31 | 1980-01-30 | Roussel Uclaf | Optically-active substituted benzyl alcohol and process for preparing it |
FR2416219A1 (fr) * | 1978-01-31 | 1979-08-31 | Roussel Uclaf | Esters d'acide acetique substitue optiquement actif et d'alcool benzylique substitue racemique ou optiquement actif, doues de proprietes insecticides, leur procede de preparation et les compositions les renfermant |
FR2423488A1 (fr) * | 1978-03-17 | 1979-11-16 | Roussel Uclaf | Nouveaux ethers dont les restes organiques comportent des atomes chiraux, leur procede de preparation et leur application au dedoublement des alcools, des phenols ou de certains composes de structure lactonique |
FR2419939A1 (fr) * | 1978-03-17 | 1979-10-12 | Roussel Uclaf | Procede de preparation d'un ether d'alcool a-cyane optiquement actif |
-
1979
- 1979-07-31 FR FR7919654A patent/FR2472570A1/fr active Granted
-
1980
- 1980-07-23 EP EP80401093A patent/EP0023454B1/fr not_active Expired
- 1980-07-23 AT AT80401093T patent/ATE3863T1/de not_active IP Right Cessation
- 1980-07-23 DE DE8080401093T patent/DE3063886D1/de not_active Expired
- 1980-07-30 HU HU80801905A patent/HU178897B/hu not_active IP Right Cessation
- 1980-07-30 JP JP10378680A patent/JPS5622776A/ja active Granted
- 1980-07-30 IE IE1595/80A patent/IE50826B1/en unknown
- 1980-07-30 CA CA000357376A patent/CA1176645A/fr not_active Expired
-
1985
- 1985-12-11 US US06/807,857 patent/US4769478A/en not_active Expired - Fee Related
-
1986
- 1986-12-03 JP JP61286886A patent/JPS62187465A/ja active Granted
-
1987
- 1987-04-10 US US07/036,890 patent/US4801723A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US4769478A (en) | 1988-09-06 |
EP0023454B1 (fr) | 1983-06-22 |
JPS636067B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1988-02-08 |
CA1176645A (fr) | 1984-10-23 |
EP0023454A3 (en) | 1981-04-29 |
IE50826B1 (en) | 1986-07-23 |
FR2472570B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1983-06-17 |
US4801723A (en) | 1989-01-31 |
HU178897B (en) | 1982-07-28 |
JPS62187465A (ja) | 1987-08-15 |
IE801595L (en) | 1981-01-31 |
JPS5622776A (en) | 1981-03-03 |
JPH0321551B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-03-22 |
FR2472570A1 (fr) | 1981-07-03 |
EP0023454A2 (fr) | 1981-02-04 |
DE3063886D1 (en) | 1983-07-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4720556A (en) | 3-oxabicyclo-(3,1,0)-hexan-2-ones | |
ATE3863T1 (de) | Verfahren zur herstellung von 6,6-dimethyl-4hydroxy-3-oxabicyclo(3.1.0)-2-hexanon und seiner aether jeglicher stereoisomerer form. | |
KR830010039A (ko) | 페닐 지방성 카복실린산 유도체의 제조방법 | |
DE1793679B2 (de) | S-d'-R-r-X-S'-Oxo-cyclopentyl)propionsSuren und deren Allylester | |
DE69731005T2 (de) | Verfahren zu Herstellung von Taxol | |
US3666798A (en) | Production of optically active chrysanthemic acid | |
ATE8781T1 (de) | Halogenierte derivate des 5-hydroxy-tetrahydro-2- furanons. | |
SE7606736L (sv) | Bestatin-foreningar och sett for framstellning derav | |
DE69109258T2 (de) | Verfahren zur stereoselektiven Umwandlung eines Diols in einen Alkohol. | |
JPS5663976A (en) | Novel sulfonated compound containing lactone ring* its manufacture and application to manufacture of cyclopropane derivative | |
JPS5612355A (en) | Manufacture of optically active alphaacyanoalcohol | |
PT69739A (fr) | Procede de preparation d'esters d'acides cyclopropane carboxyliques substitues d'alcool alpha cyane | |
DE68925947T2 (de) | Optisch wirksame Verbindungen und Verfahren zu deren Herstellung | |
JPS55136245A (en) | Optical resolution of alpha-isopropyl-p-chlorophenyl-acetic acid | |
Kang et al. | A Chiral Synthesis of a Mosquito Oviposition Pheromone | |
ATE5583T1 (de) | 4-methyl-3-formylpentensaeurealkylester, deren herstellungsverfahren, deren verwendung zur herstellung der 4-methyl-3-formyl-3-pentensaeure und die zwischenprodukte. | |
US4276230A (en) | Cyano-3-phenoxybenzyl N-1-(1-naphthyl) ethylcarbamate | |
DE2422376B2 (de) | Verfahren zur Herstellung von Zitronensäure, deren Salzen oder Estern | |
JPS57158777A (en) | 2,2,4-trimethyl-5-amyl-1,3-dioxolane | |
SU143807A1 (ru) | Способ получени эфиров N-замещенных альфа-пирролидинкарбоновых кислот | |
Saburo et al. | Studies on the Syntheses of the Pyrethrin Analogues and their Biological Activities.(I): Allethronyl Esters of Cyclopropanecarboxylic Acids (Commemoration Issue Dedicated to Professor Sankichi Takei On the Occasion of his Retirement) | |
Sakata et al. | Structural elucidation of twelve novel esters composed of five fatty acids and three new branched alcohols together with four monoterpenoids from Sancassania shanghaiensis (Acari: Acaridae) | |
JP2889359B2 (ja) | ベンゾイルエステルを用いて行う光学純度決定法 | |
JPS55162786A (en) | Glyoxylic acid derivative and its preparation | |
Shin et al. | STEREOSELECTIVE FORMATION OF α, α-DIAMINO ACID RESIDUE BY THE ADDITION OF l-α-AMINO ACID TO α-IMINO ACID |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
UEP | Publication of translation of european patent specification | ||
REN | Ceased due to non-payment of the annual fee |