Stereochemistry of the Black Tea Pigments Theacitrins A and C

July 28, 2017

Title

Stereochemistry of the Black Tea Pigments Theacitrins A and C

Author

Yosuke Matsuo, Keita Okuda, Hitomi Morikawa, Ryosuke Oowatashi, Yoshinori Saito, Takashi Tanaka

Year

2016

Journal

Journal of Natural Products

Abstract

Theacitrins A–C are yellow pigments of black tea that are produced by oxidative coupling of gallocatechins, i.e., flavan-3-ols with pyrogallol-type B-rings. However, their stereostructures have not yet been determined. In this study, DFT calculations of NMR chemical shifts of theacitrin C (1) and TDDFT calculations of the ECD spectra of theacitrinin A (5), a degradation product of theacitrin C (1), were used to determine the stereostructure of the theacitrins. Furthermore, the preparation of theacitrins A (4) and C (1) by enzymatic oxidation of an epigallocatechin (7) and epigallocatechin-3-O-gallate (2) mixture confirmed their structural relationship.

Instrument

J-725

Keywords

Circular dichroism, Absolute configuration, Natural products, Pharmaceutical