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Open AccessJournal ArticleDOI

Über Umlagerung von Phenol‐allyläthern in C‐Allyl‐phenole

L. Claisen
- 01 Oct 1912 - 
- Vol. 45, Iss: 3, pp 3157-3166
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TLDR
Salmiak as mentioned in this paper verwandelter Verbindungen in 0-Alkylderivaten and C-Derivate umzulagern, tritt diese Neigung bei den 0 A 11 y lderivaten i n stitrkstem Mn5e hervor.
Abstract
Bei Wiederauinahme meiner Arbeiten iiber die 0 A l k y l d e r i v a t e d e s A c e t e s s i g e s t e r s und verwandter Verbindungen hat sich ein bemerkenswerter Unterschied gezeigt, der zwischen den 0-Alkylderivaten mit den gewiihnlichen gesLt t ig ten A l k g l e n (Methyl, Athyl, Propyl usw.) einerseits und den %All yl'derivaten andererseits besteht. Wahrend die ersteren so gut wie gar keine Neigung zeigen, sich in die isomeren C-Derivate umzulagern, tritt diese Neigung bei den 0 A 11 y lderivaten i n stitrkstem Mn5e hervor. 0Al ly 1acetessigester wird beim Destillieren uber etwas Salmiak fast vollstiindig in 0Ally l ace t ess iges t e r verwandelt :

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Quantitative molecular simulations

TL;DR: In this paper , an overview of the present status of quantitative atomistic simulations from colleagues' and their own efforts for gas- and solution-phase processes and for the dynamics on surfaces.
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Reaktionen von (−)-Ephedrin bzw. (+)-Norpseudoephedrin und Derivaten mit N,N-Dimethylacetamid-dimethylacetal und N,N,-Dimethylformamid-dimethylacetal

TL;DR: In this paper, the reactivity of (−)-ephedrine and (+)-norpseudoephedrin (3) towards the amidacetals has been studied and the results showed that derivatives of derivatives possessing a trisubstituted amino group react with 1 a in a [3.3] sigmatopic rearrangement toortho substituted dimethyl carbamoylmethyl derivatives.
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Allylphenols as a new class of human 15‐lipoxygenase‐1 inhibitors

TL;DR: It was found that the electronic natures of allyl moiety and para substituents play the main role in radical scavenging activity and subsequently LOX inhibition potency of the synthetic inhibitors.

Synthetic approach to natural products by Claisen rearrangement of glyceraldehyde derivatives

TL;DR: In this article, a number of corynanthe-type indole alkaloids, sesquiterpenes, and steroids, including cyclopentanone 3-allyl alcohol, α-methylene-γ-butylo lactones and trans-hydrindanone-propionic acid, were synthesized from (R)- and (S)-isopropylideneglyceraldehyde derived from D-mannitol and Lascorbic acid, respectively, utilizing Claisen rearrangement as a key reaction.
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