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Hydroxycinnamoyl Amino Acids Conjugates: A Chiral Pool to Distinguish Commercially Exploited Coffea spp
by
Forzato, Cristina
, Colomban, Silvia
, Navarini, Luciano
, Berti, Federico
in
Amides - chemistry
/ Amino acids
/ Amino Acids - chemistry
/ Chromatography
/ Circular Dichroism
/ Coffea - chemistry
/ Coffee
/ coffee beans
/ Coumaric Acids - chemistry
/ Dimerization
/ hydroxycinnamoyl amides
/ LC-MS
/ Mass Spectrometry
/ Stereoisomerism
/ Time Factors
2020
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Hydroxycinnamoyl Amino Acids Conjugates: A Chiral Pool to Distinguish Commercially Exploited Coffea spp
by
Forzato, Cristina
, Colomban, Silvia
, Navarini, Luciano
, Berti, Federico
in
Amides - chemistry
/ Amino acids
/ Amino Acids - chemistry
/ Chromatography
/ Circular Dichroism
/ Coffea - chemistry
/ Coffee
/ coffee beans
/ Coumaric Acids - chemistry
/ Dimerization
/ hydroxycinnamoyl amides
/ LC-MS
/ Mass Spectrometry
/ Stereoisomerism
/ Time Factors
2020
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Hydroxycinnamoyl Amino Acids Conjugates: A Chiral Pool to Distinguish Commercially Exploited Coffea spp
by
Forzato, Cristina
, Colomban, Silvia
, Navarini, Luciano
, Berti, Federico
in
Amides - chemistry
/ Amino acids
/ Amino Acids - chemistry
/ Chromatography
/ Circular Dichroism
/ Coffea - chemistry
/ Coffee
/ coffee beans
/ Coumaric Acids - chemistry
/ Dimerization
/ hydroxycinnamoyl amides
/ LC-MS
/ Mass Spectrometry
/ Stereoisomerism
/ Time Factors
2020
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Hydroxycinnamoyl Amino Acids Conjugates: A Chiral Pool to Distinguish Commercially Exploited Coffea spp
Journal Article
Hydroxycinnamoyl Amino Acids Conjugates: A Chiral Pool to Distinguish Commercially Exploited Coffea spp
2020
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Overview
The synthesis of five hydroxycinnamoyl amides (HCAs) was accomplished and their identification and quantification in the green coffee bean samples of Coffea arabica, Coffea canephora, and Coffea liberica was performed. The HCAs p-coumaroyl-N-tyrosine 1b, caffeoyl-N-phenylalanine 2b, caffeoyl-N-tyrosine 3b, and p-coumaroyl-N-tryptophan 4b were characteristic of the C. canephora species while caffeoyl-N-tryptophan 5b was present in both C. canephora and C. arabica, but with higher content in C. canephora. The HCAs presence was also analyzed in C. liberica for the first time and none of the targeted compounds was found, indicating that this species is very similar to C. arabica species. Between C. canephora samples from various origins, significant differences were observed regarding the presence of all the HCAs, with C. canephora from Tanzania containing all five derivatives.
Publisher
MDPI AG,MDPI
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