Synthesis 2014; 46(13): 1779-1787
DOI: 10.1055/s-0033-1341083
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Tea Catechin Lactone Metabolite Analogues with a 2′-Hydroxyphenyl Group

Authors

  • Masahiro Hamada*

    a   Department of Biotechnology, Faculty of Engineering, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan
    b   Biotechnology Research Center, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan   Fax: +81(766)562498   Email: hamada@pu-toyama.ac.jp   Email: nori@pu-toyama.ac.jp
  • Shunichi Naruse

    a   Department of Biotechnology, Faculty of Engineering, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan
  • Misaki Wada

    a   Department of Biotechnology, Faculty of Engineering, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan
  • Takao Kishimoto

    a   Department of Biotechnology, Faculty of Engineering, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan
    b   Biotechnology Research Center, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan   Fax: +81(766)562498   Email: hamada@pu-toyama.ac.jp   Email: nori@pu-toyama.ac.jp
  • Noriyuki Nakajima*

    a   Department of Biotechnology, Faculty of Engineering, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan
    b   Biotechnology Research Center, Toyama Prefectural University, Imizu, Toyama 939-0398, Japan   Fax: +81(766)562498   Email: hamada@pu-toyama.ac.jp   Email: nori@pu-toyama.ac.jp
Further Information

Publication History

Received: 10 February 2014

Accepted after revision: 11 March 2014

Publication Date:
17 April 2014 (online)


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Abstract

Tea catechins such as epicatechin, epigallocatechin, epicatechin gallate and epigallocatechin gallate afford many metabolites, including γ-valerolactone derivatives, through metabolic pathways in the human body. Two of these γ-valerolactone metabolite analogues with a 2′-hydroxyphenyl group were synthesized as optically active authentic standards.