Literature DB >> 20386808

General synthesis of epi-series catechins and their 3-gallates: reverse polarity strategy.

Ken Ohmori1, Takahisa Yano, Keisuke Suzuki.   

Abstract

A general synthetic route to the epi-series catechins was developed based on the reverse polarity strategy. Aromatic nucleophilic substitution reaction followed by the sulfinyl-metal exchange and cyclization enabled stereo-controlled access to various members of epi-series catechins and their 3-gallates.

Entities:  

Mesh：

Substances：

Year:  2010        PMID： 20386808     DOI： 10.1039/c003464a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN： 1477-0520            Impact factor:   3.876


  4 in total

1.  Structural elucidation and bioactivity of biflavonoids from the stems of Wikstroemia taiwanensis.

Authors:  Li-Yin Chen; Ih-Sheng Chen; Chien-Fang Peng
Journal:  Int J Mol Sci       Date:  2012-01-18       Impact factor: 6.208

2.  Procyanidins Negatively Affect the Activity of the Phosphatases of Regenerating Liver.

Authors:  Sven Stadlbauer; Pablo Rios; Ken Ohmori; Keisuke Suzuki; Maja Köhn
Journal:  PLoS One       Date:  2015-07-30       Impact factor: 3.240

Review 3.  Chiral Flavonoids as Antitumor Agents.

Authors:  Cláudia Pinto; Honorina Cidade; Madalena Pinto; Maria Elizabeth Tiritan
Journal:  Pharmaceuticals (Basel)       Date:  2021-12-05

4.  Tea silkworm droppings as an enriched source of tea flavonoids.

Authors:  Tzu-Yun Chou; Meei-Ju Yang; Shih-Kung Tseng; Shoei-Sheng Lee; Chia-Chuan Chang
Journal:  J Food Drug Anal       Date:  2017-01-25       Impact factor: 6.157
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.