GB1461440A - 2,5-substituted tetrahydrofurans and their production - Google Patents
2,5-substituted tetrahydrofurans and their productionInfo
- Publication number
- GB1461440A GB1461440A GB2713774A GB2713774A GB1461440A GB 1461440 A GB1461440 A GB 1461440A GB 2713774 A GB2713774 A GB 2713774A GB 2713774 A GB2713774 A GB 2713774A GB 1461440 A GB1461440 A GB 1461440A
- Authority
- GB
- United Kingdom
- Prior art keywords
- production
- substituted tetrahydrofurans
- compound
- formula
- tetrahydrofurans
- 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
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
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/16—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
1461440 6 - Oxo - octyl - tetrahydrofuranyloctoic acid trimethylsilyl ester GRINDSTEDVAERKET AS 19 June 1974 27137/74 Heading C3S [Also in Division C2] The compound of the Formula X is prepared by reacting the compound of the Formula IX with hexamethyldisilazane and trimethylchlorosilane in the presence of pyridine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2713774A GB1461440A (en) | 1974-06-19 | 1974-06-19 | 2,5-substituted tetrahydrofurans and their production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2713774A GB1461440A (en) | 1974-06-19 | 1974-06-19 | 2,5-substituted tetrahydrofurans and their production |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1461440A true GB1461440A (en) | 1977-01-13 |
Family
ID=10254826
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2713774A Expired GB1461440A (en) | 1974-06-19 | 1974-06-19 | 2,5-substituted tetrahydrofurans and their production |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1461440A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0159528A1 (en) * | 1984-04-02 | 1985-10-30 | E.R. Squibb & Sons, Inc. | Tetrahydrofuranyl substituted prostaglandin analogs |
-
1974
- 1974-06-19 GB GB2713774A patent/GB1461440A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0159528A1 (en) * | 1984-04-02 | 1985-10-30 | E.R. Squibb & Sons, Inc. | Tetrahydrofuranyl substituted prostaglandin analogs |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |