thio-ester
Sign in to savethumb|class=skin-invert-image|right|150px|General structure of a thioester, where R and R' are organyl groups, or H in the case of R. In organic chemistry, thioesters are organosulfur compounds with the molecular structure . They are analogous to carboxylate esters () with the sulfur in the thioester replacing oxygen in the carboxylate ester, as implied by the thio- prefix. They are the product of esterification of a carboxylic acid () with a thiol (). In biochemistry, the best-known thioesters are derivatives of coenzyme A, e.g., acetyl-CoA. The R and R' represent organyl groups, or H in the
In the Vinony graph
Within Vinony's link graph, thio-ester is referenced by 305 other articles, and connects out to ester, carboxylic acid chloride and hydrogen.
It sits within the topics Functional groups, Origin of life and Thioesters.
Its subject is documented across 28 Wikipedia language editions.
Wikidata facts
- Subclass of
- organosulfur compound
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- Commons category
- Thioesters
- topic's main category
- Category:Thioesters
- SMARTS notation
- [#6][#6](=[OX1])[#16][#6]
Sources (2)
via Wikidata · CC0
Article · Nederlands
Een thio-ester is in de organische chemie een functionele groep, die gekenmerkt wordt door de binding tussen een zwavelatoom en een acylgroep. Dat zwavelatoom is verder gebonden aan een koolwaterstofgroep (R'). De algemene formule is R-S-CO-R'.
Abstract from DBpedia / Wikipedia · CC BY-SA