Invention Grant
- Patent Title: Process for preparation of adjacently disubstituted ketones
- Patent Title (中): 相邻二取代酮制备方法
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Application No.: US149584Application Date: 1980-05-14
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Publication No.: US4315032APublication Date: 1982-02-09
- Inventor: Ryoji Noyori , Masaaki Suzuki , Seizi Kurozumi
- Applicant: Ryoji Noyori , Masaaki Suzuki , Seizi Kurozumi
- Applicant Address: JPX Osaka
- Assignee: Teitin Limited
- Current Assignee: Teitin Limited
- Current Assignee Address: JPX Osaka
- Priority: JPX54/60293 19790518
- Main IPC: C07B37/02
- IPC: C07B37/02 ; A61K31/557 ; C07B31/00 ; C07C45/00 ; C07C45/69 ; C07C45/70 ; C07C45/72 ; C07C45/75 ; C07C49/493 ; C07C49/517 ; C07C49/743 ; C07C49/747 ; C07C49/753 ; C07C67/00 ; C07C225/20 ; C07C401/00 ; C07C405/00 ; C07D309/12 ; C07F7/18 ; C07C177/00
Abstract:
A novel 7-hydroxyprostaglandin E.sub.1, or a stereoisomer thereof, or a protected derivative thereof, having the following formula: ##STR1## wherein R.sup.8 represents H, CH.sub.3 or C.sub.2 H.sub.5, R.sup.9 represents H or CH.sub.3, R.sup.10 and R.sup.11 are identical or different, and each represents H, tetrahydropyranyl or t-butyldimethylsilyl. Also provided is a process for producing an adjacently disubstituted ketone including the above compounds, i.e. 7-oxoprostaglandin, etc. which comprises reacting an .alpha.,.beta.-unsaturated carbonyl compound with a cuprous salt and an organolithium compound in an aprotic inert organic medium in the presence of trialkylphosphine, the amounts of said cuprous salt and said organolithium compound being substantially equimolar, and reacting the product with a protected acetal derivative of an organic carbonyl compound or an aldehyde in the presence of a Lewis acid, if necessary, followed by reacting the product with a proton donor.
Public/Granted literature
- US6065408A Security case Public/Granted day:2000-05-23
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