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Org Lett ; 21(13): 5147-5151, 2019 07 05.
Article in English | MEDLINE | ID: mdl-31247775

ABSTRACT

Racemic trimethylallantoin monomer (1), mesomeric and racemic trimethylallantoin dimers (2 and 3), were isolated from tea. Two pairs of optically pure enantiomers (1a, 1b and 3a, 3b) were separated by chiral column from the two racemes (1 and 3). Their structures were elucidated by a combination of extensive spectroscopic techniques, single-crystal X-ray diffraction, and experimental and calculated electronic circular dichroism. A novel caffeine catabolic pathway was proposed based on the caffeine stable isotopic tracer experiments.


Subject(s)
Caffeine/chemistry , Caffeine/metabolism , Dimerization , Tea/metabolism , Methylation , Models, Molecular , Molecular Conformation , Stereoisomerism
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