2018
DOI: 10.20944/preprints201802.0151.v1
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The Use of Anisaldehyde Sulfuric Acid as an Alternative Spray Reagent in TLC Analysis Reveals Three Classes of Compounds in the Genus <em>Usnea</em> Adans. (Parmeliaceae, lichenized Ascomycota)

Abstract: Presence and identity of secondary metabolites are two of the main components of lichen taxonomy. Aromatic compounds formed via the acetyl-polymalonate pathway are the most studied lichen substances. In addition, compounds derived from the mevalonic acid pathway (e.g. terpenes and steroids) are sometimes detected in the medulla. However, their identity and value as diagnostic characters in the genus Usnea are yet poorly understood despite the fact that they were mentioned in several taxonomical papers. We conc… Show more

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Cited by 15 publications
(14 citation statements)
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(22 reference statements)
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“…Monoterpenes, triterpenes and steroids usually appear as blue, purple and gray spots [23]. Derivatization using p-anisaldehyde/sulfuric acid creates brown spots for diterpenes [22], while triterpenes produce a blue violet color under visible/white light, and a reddish or blue color under UV at 366 nm [24,25].…”
Section: Resultsmentioning
confidence: 99%
“…Monoterpenes, triterpenes and steroids usually appear as blue, purple and gray spots [23]. Derivatization using p-anisaldehyde/sulfuric acid creates brown spots for diterpenes [22], while triterpenes produce a blue violet color under visible/white light, and a reddish or blue color under UV at 366 nm [24,25].…”
Section: Resultsmentioning
confidence: 99%
“…Then, the chromatograms were sprayed with 10% H 2 SO 4 in ethanol and heated at 100 °C for 10 min. The compounds with comparable R f in TLC were mixed homogeneously, as reported by [ 53 ].…”
Section: Methodsmentioning
confidence: 99%
“…The aqueous basic solution was extracted with ether, and the pooled ether extracts were evaporated till dryness under reduced pressure. The hydrohalogenation and/or amination reactions were monitored by precoated thin-layer chromatography (TLC) plates (silica gel 60, GF 254 (60-250 mesh), Merck, Germany) using a solvent system (hexane: methylene chloride (1:1)) and p-anisaldehyde sulfuric acid spray according to Gerlacha et al [69], as visualizing agent. The TLC plates were heated for about 5 min at 100°C, and resultant oil from hydrohalogenation and/or amination reactions was analyzed directly by GC-MS. GC-MS analysis of synthesized MMDA.…”
Section: Chemical Synthesis Of Mmdamentioning
confidence: 99%