“…Thiol compounds were formed by H 2 S produced during the degradation of sulfur-containing amino acids in the Maillard reaction ( Wei et al, 2019 ). Among them, 2-methyl-3-furanthiol was responsible for roasted, coffee-like, and meaty aromas, and 2-furfurylthiol was the key odorant in cooked meat ( Zheng et al, 2023 ). Furthermore, sulfur-substituted furans such as furfuryl sulfide, bis(2-furfuryl)disulfide, and 2-methyl-5-(methylthio)-furan have been found to make a significant contribution to a strong meaty flavor or roasted note ( Zhang et al, 2022 ).…”