Synthese des Syringins

Pauly, H.; Strassberger, L

doi:10.1002/cber.19290620865

Cited by 17 publications

(1 citation statement)

References 2 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The product was later treated with boiling dimethyl-p-toluidine to yield syringaldehyde. The synthesis was improved by substituting ethyl mesoxalate with chloral hydrate (Pauly and Strassberger 1929), and their reaction is outlined in Fig. 2.…”

Section: Synthesis Of Syringaldehydementioning

confidence: 99%

A concise review of the natural existance, synthesis, properties, and applications of syringaldehyde

Ibrahim

Balakrishnan

Shamsudeen

et al. 2012

BioRes

View full text Add to dashboard Cite

Syringaldehyde is a promising aromatic aldehyde that no longer deserves to remain in obscurity. It possesses worthy bioactive properties and is, therefore, used in pharmaceuticals, food, cosmetics, textiles, pulp and paper industries, and even in biological control applications. Mostly, the synthetic form of syringaldehyde is being used. This review serves as an appraisal of potential research and commercialization of naturally occurring syringaldehyde beyond the scope of the food and cosmetic industries. This article also provides a comprehensive account of the various conventional extraction and chromatographic techniques used in the separation, isolation, and quantification of syringaldehyde. Further, to understand this unique compound, a brief outline on the natural formation of syringaldehyde in lignin is accentuated in this article.

show abstract

Section: Synthesis Of Syringaldehydementioning

confidence: 99%

A concise review of the natural existance, synthesis, properties, and applications of syringaldehyde

Ibrahim

Balakrishnan

Shamsudeen

et al. 2012

BioRes

View full text Add to dashboard Cite

show abstract

The Aldol Condensation

Nielsen

Houlihan²

2011

Organic Reactions

View full text Add to dashboard Cite

The aldol condensation takes its name from aldol (3‐hydroxybutanal) a name introduced by Wurtz who first prepared the beta‐hydroxy aldehyde from acetaldehdye in 1872. The aldol condensation includes reactions producing beta‐hydroxy aldehydes or beta‐hydroxy ketones by self condensations or mixed condensations of aldehydes and ketones as well as reactions leading to alpha, beta‐unsaturated aldehydes or alpha,beta‐unsaturated ketones formed by dehydration of intermediate beta‐aldols or beta‐ketals. The Claisen‐Schmidt condensation is most often taken to be the condensation of an aromatic aldehyde or ketone usually in the presence of a basic catalyst. The term aldol condensation has also been applied to many other condensations involving the reaction of an aldehyde or ketone. These condenations are discussed. The present review includes examples that are solely condensation reactions of aldehydes and ketones.

show abstract