Prostaglandinderivate und Verfahren zu ihrer Herstellung

Prostaglandin analogues (II) are new compds. prepared by reacting water at 0-60 C with disulphenic esters of formula I, which may have the exo- or endv configuration. (which n is 1-8; a is 0-4; R15 is C1-4 alkyl or -CH2CCl3: Y = i-butyl, t-butyl, 3,3- difluorobutyl, 4,4-difluorobutyl, or 4,4,4-trifl...

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Bibliographic Details
Main Author EDWARD PIKE,JOHN
Format Patent
LanguageGerman
Published 02.07.1970
Subjects
ACYCLIC OR CARBOCYCLIC COMPOUNDS
BEER
BIOCHEMISTRY
CHEMISTRY
ENZYMOLOGY
FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE
METALLURGY
MICROBIOLOGY
MUTATION OR GENETIC ENGINEERING
ORGANIC CHEMISTRY
SPIRITS
VINEGAR
WINE
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Summary:Prostaglandin analogues (II) are new compds. prepared by reacting water at 0-60 C with disulphenic esters of formula I, which may have the exo- or endv configuration. (which n is 1-8; a is 0-4; R15 is C1-4 alkyl or -CH2CCl3: Y = i-butyl, t-butyl, 3,3- difluorobutyl, 4,4-difluorobutyl, or 4,4,4-triflurorbutyl; is approx. indicates that the -(CH2)n-COOR15 group is in alpha- or beta-configuration relative to the ring; R6 is C1-5 alkyl) Advantages/uses:- the cpds. II and III and their derivatives are analogous to prostaglandin E, prostaglandin F and prostaglandin A in their bilogical activity, but are much more specific in action. As the present compounds have a narrower biological spectrum, their use is generally attended by a lesser degree of undesired side actions than for the natural prostaglandins. In addition, some of the synthetic compounds show a higher biological response than the natural prostaglandins in a specific area.
Bibliography:Application Number: DE19691937908