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E. Schlittler

Bio: E. Schlittler is an academic researcher from Ciba Specialty Chemicals. The author has an hindex of 3, co-authored 3 publications receiving 240 citations.

Papers
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Journal ArticleDOI
TL;DR: The sedative principle of Rauwolfia serpentina Benth has been isolated in pure crystalline form and its chemistry and pharmacology has been studied as discussed by the authors, and its properties and properties have been investigated.
Abstract: The sedative principle ofRauwolfia serpentina Benth. has been isolated in pure crystalline form and its chemistry and pharmacology has been studied.

199 citations

Journal ArticleDOI
TL;DR: Durch alkalische Hydrolyse wird Reserpin in Reserpinsäure, 3,4,5-Trimethoxybenzoesäure und Methanol gespalten anderer Spaltstücken wieder resynthetisieren.
Abstract: Durch alkalische Hydrolyse wird Reserpin in Reserpinsaure, 3,4,5-Trimethoxybenzoesaure und Methanol gespalten. Das Esteralkaloid liess sich aus diesen Spaltstucken wieder resynthetisieren.

27 citations

Journal ArticleDOI
TL;DR: In this article, the Stellung der einen Methoxylgruppe festgelegt, wogegen die Haftstellen der drei weiteren funktionelle Gruppen noch nicht gesichert sind.
Abstract: Bei der Permanganatoxydation und der Kalischmelze der Reserpinsaure wurden 4-Methoxy-oxalylanthranilsaure und 5-Oxyisophtalsaure isoliert. Als Arbeitshypothese wird deshalb fur Reserpinsaure eine Yohimbanstruktur postuliert. Durch die obigen Abbauergebnisse ist die Stellung der einen Methoxylgruppe festgelegt, wogegen die Haftstellen der drei weiteren funktionellen Gruppen noch nicht gesichert sind.

20 citations


Cited by
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Journal ArticleDOI
TL;DR: This review covers the literature on simple indole alkaloid and those with a nonrearranged monoterpenoid unit and newly isolated alkaloids, structure determinations, total syntheses and biological activities.

531 citations

Journal ArticleDOI
TL;DR: This paper shows by example some total syntheses which draw from strategy-enabling advances in methodology and shows how these capabilities can be used to discover and develop new agents of potential pharmaceutical value without recourse to the natural product itself.
Abstract: Natural products have been a rich source of agents of value in medicine. They have also inspired, at various levels, the fashioning of nonnatural agents of pharmaceutical import. Hitherto, these nonnatural derivatives have been primarily synthesized by manipulating the natural product. As a consequence of major innovations in the subscience of synthetic methodology, the capacity of synthesis to deal with molecules of considerable complexity has increased dramatically. In this paper, we show by example some total syntheses which draw from strategy-enabling advances in methodology. Moreover, we show how these capabilities can be used to discover and develop new agents of potential pharmaceutical value without recourse to the natural product itself.

322 citations

Book ChapterDOI
01 Jan 1966
TL;DR: The aim of the present Chapter is to review and discuss the pertinent literature dealing with fundamental problems of Rauwolfia alkaloids and benzoquinolizines rather than to review in detail the enormous literature on the pharmacology of these agents.
Abstract: In 1955 Shore, Brodie and coworkers (Shore, Silver and Brodie 1955, Pletscher, Shore and Brodie 1955) discovered that reserpine caused a marked decrease in the concentration of 5-hydroxytryptamine (5-HT) in tissues and a concomitant rise in the urinary excretion of the 5-HT metabolite 5-hydroxyindoleacetic acid. The deep physiological significance of this discovery became even more evident when reserpine soon afterwards was found to affect tissue catecholamines in a similar manner, an effect leading to block of adrenergic transmission mechanisms (Carlsson and Hillarp 1956a, Bertler, Carlsson and Rosengren 1956). Since then numerous papers have appeared, in which the effects of Rauwolfia alkaloids and a group of similarly acting benzoquinolizines (Pletscher, Besendorf and Bachtold 1958) have been further analyzed. Particular interest has been focussed on the mechanism of action on the abovementioned amines and on the relationship between this action and the various pharmacological effects of Rauwolfia alkaloids and benzoquinolizines. It is the aim of the present Chapter to review and discuss the pertinent literature dealing with these fundamental problems rather than to review in detail the enormous literature on the pharmacology of these agents.

318 citations

Journal ArticleDOI
Robert B. Woodward1, F. E. Bader1, H. Bickel1, A. J. Frey1, R. W. Kierstead1 

228 citations