2003
DOI: 10.1201/9780203912812.ch34
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On the Role of 3-Methyl-2-Butene-1-Thiol in Beer Flavor

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Cited by 2 publications
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“…Most of the isotopically labeled internal standards were synthesized as listed in a previous study: In addition, [ 2 H 2 ]-methylpropanol, [ 2 H 2 ]-( Z )-3-hexenol, [ 2 H 2 ]-butanoic acid, [ 2 H 5 ]-ethyl pentanoate, [ 2 H 3 ]-hexanoic acid, [ 13 C 2 ]-3-hydroxy-4,5-dimethyl-2­(5 H )-furanone, [ 2 H 2 ]-3-methylbutanoic acid, [ 2 H 2 ]-octanoic acid, and [ 13 C 2 ]-phenylacetaldehyde were synthesized as previously reported. [ 13 C 2 ]-Phenylacetic acid was bought from Merck.…”
Section: Methodsmentioning
confidence: 99%
“…Most of the isotopically labeled internal standards were synthesized as listed in a previous study: In addition, [ 2 H 2 ]-methylpropanol, [ 2 H 2 ]-( Z )-3-hexenol, [ 2 H 2 ]-butanoic acid, [ 2 H 5 ]-ethyl pentanoate, [ 2 H 3 ]-hexanoic acid, [ 13 C 2 ]-3-hydroxy-4,5-dimethyl-2­(5 H )-furanone, [ 2 H 2 ]-3-methylbutanoic acid, [ 2 H 2 ]-octanoic acid, and [ 13 C 2 ]-phenylacetaldehyde were synthesized as previously reported. [ 13 C 2 ]-Phenylacetic acid was bought from Merck.…”
Section: Methodsmentioning
confidence: 99%
“…Some authors [1,4,8,[18][19][20][21][22][23] described also the polyphenols such as catechin, epicatechin and quercitin, as protectors of the formation of this sunstruck flavor. The protective effect of polyphenols was described as (1) quenching both the singlet-and triplet-excited states of riboflavin with rates close to the diffusion control [22], (2) to preserve riboflavin absorbance in light-exposed model beers by quenching its excited energy state, and (3) a possible extraction of electrons by isohumulones from the polyphenols and the latter from photo-reduced riboflavin returning this to its original state [4].…”
Section: Introductionmentioning
confidence: 99%