GB1250869A - - Google Patents
Info
- Publication number
- GB1250869A GB1250869A GB1250869DA GB1250869A GB 1250869 A GB1250869 A GB 1250869A GB 1250869D A GB1250869D A GB 1250869DA GB 1250869 A GB1250869 A GB 1250869A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cyclohex
- trimethyl
- hydroxy
- triphenyl
- penta
- 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
- -1 polyene compounds Chemical class 0.000 abstract 7
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 abstract 3
- PSQYTAPXSHCGMF-BQYQJAHWSA-N β-ionone Chemical compound CC(=O)\C=C\C1=C(C)CCCC1(C)C PSQYTAPXSHCGMF-BQYQJAHWSA-N 0.000 abstract 3
- SFEOKXHPFMOVRM-UHFFFAOYSA-N (+)-(S)-gamma-ionone Natural products CC(=O)C=CC1C(=C)CCCC1(C)C SFEOKXHPFMOVRM-UHFFFAOYSA-N 0.000 abstract 2
- RANZORNCENEFNN-UHFFFAOYSA-M [3-methyl-5-(2,6,6-trimethyl-3-oxocyclohexen-1-yl)penta-2,4-dienyl]-triphenylphosphanium bromide Chemical compound [Br-].O=C1C(=C(C(CC1)(C)C)C=CC(=CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C)C RANZORNCENEFNN-UHFFFAOYSA-M 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 150000004714 phosphonium salts Chemical class 0.000 abstract 2
- JUFKQNCQDFHWFD-UHFFFAOYSA-N (3S,7E,9R)-3,9-dihydroxy-5,7-megastigmadiene Natural products CC(O)C=CC1=C(C)CC(O)CC1(C)C JUFKQNCQDFHWFD-UHFFFAOYSA-N 0.000 abstract 1
- PPEXHEZQKRHDII-UHFFFAOYSA-N 3-(3-hydroxy-3-methylpenta-1,4-dienyl)-2,4,4-trimethylcyclohex-2-en-1-ol Chemical compound CC1=C(C=CC(C)(O)C=C)C(C)(C)CCC1O PPEXHEZQKRHDII-UHFFFAOYSA-N 0.000 abstract 1
- JUFKQNCQDFHWFD-MNOVXSKESA-N 3-Hydroxy-beta-ionol Natural products C[C@@H](O)C=CC1=C(C)C[C@H](O)CC1(C)C JUFKQNCQDFHWFD-MNOVXSKESA-N 0.000 abstract 1
- HFRZSVYKDDZRQY-AATRIKPKSA-N 3-Hydroxy-beta-ionone Chemical compound CC(=O)\C=C\C1=C(C)CC(O)CC1(C)C HFRZSVYKDDZRQY-AATRIKPKSA-N 0.000 abstract 1
- LICNQDPDQQOXCU-FYJFLYSWSA-N 3-Hydroxy-beta-ionone Natural products CC(=O)\C=C\C1=C(C)[C@@H](O)CCC1(C)C LICNQDPDQQOXCU-FYJFLYSWSA-N 0.000 abstract 1
- HXQRIVAUIRBXMR-UHFFFAOYSA-N 4-(3-hydroxy-3-methylpenta-1,4-dienyl)-3,5,5-trimethylcyclohex-3-en-1-ol Chemical compound CC1=C(C=CC(C)(O)C=C)C(C)(C)CC(O)C1 HXQRIVAUIRBXMR-UHFFFAOYSA-N 0.000 abstract 1
- JUFKQNCQDFHWFD-AATRIKPKSA-N 4-[(e)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-3-en-1-ol Chemical compound CC(O)\C=C\C1=C(C)CC(O)CC1(C)C JUFKQNCQDFHWFD-AATRIKPKSA-N 0.000 abstract 1
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- CMSYAQMBQAWCLD-UHFFFAOYSA-N [2,4,4-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-en-1-yl] acetate Chemical compound CC(=O)OC1CCC(C)(C)C(C=CC(C)=O)=C1C CMSYAQMBQAWCLD-UHFFFAOYSA-N 0.000 abstract 1
- TXHARUYWUGDGQT-UHFFFAOYSA-N [4-(3-acetyloxybut-1-ynyl)-3,5,5-trimethylcyclohex-3-en-1-yl] acetate Chemical compound CC(=O)OC(C)C#CC1=C(C)CC(OC(C)=O)CC1(C)C TXHARUYWUGDGQT-UHFFFAOYSA-N 0.000 abstract 1
- JFNJSIKHHNVBEF-UHFFFAOYSA-M [Br-].OC1C(=C(C(CC1)(C)C)C=CC(=CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C)C Chemical compound [Br-].OC1C(=C(C(CC1)(C)C)C=CC(=CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C)C JFNJSIKHHNVBEF-UHFFFAOYSA-M 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229930002839 ionone Natural products 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 229910001623 magnesium bromide Inorganic materials 0.000 abstract 1
- RMGJCSHZTFKPNO-UHFFFAOYSA-M magnesium;ethene;bromide Chemical compound [Mg+2].[Br-].[CH-]=C RMGJCSHZTFKPNO-UHFFFAOYSA-M 0.000 abstract 1
- 229910052987 metal hydride Inorganic materials 0.000 abstract 1
- 150000004681 metal hydrides Chemical class 0.000 abstract 1
- HFRZSVYKDDZRQY-UHFFFAOYSA-N rac-3-Hydroxy-beta-ionone Natural products CC(=O)C=CC1=C(C)CC(O)CC1(C)C HFRZSVYKDDZRQY-UHFFFAOYSA-N 0.000 abstract 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/24—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/32—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen
- C07C1/34—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen reacting phosphines with aldehydes or ketones, e.g. Wittig reaction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/06—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms
- C07C403/08—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms by hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/06—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms
- C07C403/10—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms by etherified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/14—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms
- C07C403/16—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms not being part of —CHO groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/54—Quaternary phosphonium compounds
- C07F9/5442—Aromatic phosphonium compounds (P-C aromatic linkage)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1172669A CH517053A (de) | 1969-08-01 | 1969-08-01 | Verfahren zur Herstellung von Polyenverbindungen |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1250869A true GB1250869A (enrdf_load_stackoverflow) | 1971-10-20 |
Family
ID=4376304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1250869D Expired GB1250869A (enrdf_load_stackoverflow) | 1969-08-01 | 1970-07-16 |
Country Status (7)
Country | Link |
---|---|
BE (1) | BE754225A (enrdf_load_stackoverflow) |
CH (1) | CH517053A (enrdf_load_stackoverflow) |
DE (1) | DE2037935A1 (enrdf_load_stackoverflow) |
FR (1) | FR2059582B1 (enrdf_load_stackoverflow) |
GB (1) | GB1250869A (enrdf_load_stackoverflow) |
NL (1) | NL7010549A (enrdf_load_stackoverflow) |
SE (1) | SE366738B (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2653838A1 (de) * | 1975-11-30 | 1977-06-02 | Hoffmann La Roche | Polyenverbindungen |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4000198A (en) * | 1975-06-09 | 1976-12-28 | Hoffmann-La Roche Inc. | Hydroxy-acetylene-substituted cyclohexenone |
US4098827A (en) * | 1977-01-17 | 1978-07-04 | Hoffmann-La Roche Inc. | 1-(2,6,6-Trimethyl-3-hydroxy-1-cyclohexen-1-yl)-3-methyl-penta-1,4-diene[or 1-yn-4-EN]-3-ols |
USRE30260E (en) | 1977-01-17 | 1980-04-22 | Hoffmann-La Roche Inc. | 1-(2,6,6-Trimethyl-3-hydroxy-1-cyclohexen-1-yl)-3-methyl-penta-1,4-diene[or 1-yn-4-en]-3-ols |
DK171297B1 (da) * | 1987-03-27 | 1996-08-26 | Hoffmann La Roche | Fremgangsmåde til fremstilling af cyclohexenderivater som mellemprodukter til fremstilling af zeaxanthin samt cyclohexenderivater |
-
0
- BE BE754225D patent/BE754225A/xx unknown
-
1969
- 1969-08-01 CH CH1172669A patent/CH517053A/de not_active IP Right Cessation
-
1970
- 1970-07-16 NL NL7010549A patent/NL7010549A/xx unknown
- 1970-07-16 GB GB1250869D patent/GB1250869A/en not_active Expired
- 1970-07-21 FR FR707026764A patent/FR2059582B1/fr not_active Expired
- 1970-07-28 SE SE10381/70A patent/SE366738B/xx unknown
- 1970-07-30 DE DE19702037935 patent/DE2037935A1/de active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2653838A1 (de) * | 1975-11-30 | 1977-06-02 | Hoffmann La Roche | Polyenverbindungen |
Also Published As
Publication number | Publication date |
---|---|
CH517053A (de) | 1971-12-31 |
FR2059582B1 (enrdf_load_stackoverflow) | 1973-01-12 |
DE2037935A1 (de) | 1971-02-11 |
NL7010549A (enrdf_load_stackoverflow) | 1971-02-03 |
BE754225A (fr) | 1971-02-01 |
FR2059582A1 (enrdf_load_stackoverflow) | 1971-06-04 |
SE366738B (enrdf_load_stackoverflow) | 1974-05-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DeBruin et al. | Stereochemistry of nucleophilic displacement at phosphorus in some phosphetanium salts | |
GB1250869A (enrdf_load_stackoverflow) | ||
GB1171155A (en) | Improvements in or relating to Cycloalkane Derivatives and the manufacture thereof | |
JP3878748B2 (ja) | ホスホニウム塩の製造方法、ホスホニウム塩及びリコペンの製造方法 | |
GB1288436A (enrdf_load_stackoverflow) | ||
GB624118A (en) | Improvements in and relating to the preparation of substituted ª†-hydroxypropylamines | |
Marshall et al. | New synthetic approach to hydroazulenes | |
GB1514076A (en) | Carotenoid and process for the manufacture thereof | |
EP0070798A3 (de) | Mikrobizide und wuchsregulierende Mittel | |
Balaban et al. | Δ3-Dihydropyrans and tetrahydropyrans by reduction of pyrylium salts with sodium borohydride in acetic acid | |
SE7413025L (enrdf_load_stackoverflow) | ||
McCorkindale et al. | The structure and chemistry of pebrolide, desacetylpebrolide and 1-deoxypebrolide, sesquiterpene benzoates from Penicillium brevicompactum | |
KR850001752A (ko) | 3-사이클로알킬-1-(1,3-디옥산-5-일)-2-(1,2,4-트리아졸-1-일)-프로판-1-온 및 프로판-1-올의 제조방법 | |
GB1421129A (en) | Process for preparing heptadec-16-en-1,2,4-triol derivatives | |
Speed et al. | Wittig reaction using a stabilized phosphorus ylid: An efficient and stereoselective synthesis of ethyl trans-cinnamate | |
US2497732A (en) | Hydroxypyridines and processes of preparing the same | |
GB1436378A (en) | Prostaglandin derivatives | |
IE32553B1 (en) | A process for the manufacture of polyene compounds | |
GB936336A (en) | Preparation of symmetrical polyene compounds | |
DE2252719A1 (de) | Verfahren zur herstellung von aldehyden aus oxiranverbindungen | |
GB1448357A (en) | Process for preparing dihydric phenol derivatives | |
GB1391806A (en) | Phosphonium salts and a process for the preparation thereof | |
US2532137A (en) | Diphenyl-t-6-hydroxydehydroabietinol | |
ES290324A1 (es) | Procedimiento para la obtención de nuevos ésteres fosfóricos de esteroides | |
GB1293857A (en) | Cyclopropane carboxylic acid esters and a process for the manufacture thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |