Selective synthesis of the resveratrol analogue 4,4′-dihydroxy-trans-stilbene and stilbenoids modification by fungal peroxygenases-Reference-Cited by-同舟云学术

Selective synthesis of the resveratrol analogue 4,4′-dihydroxy-trans-stilbene and stilbenoids modification by fungal peroxygenases

Published:2018 Issue:9 Volume:8 Page:2394-2401
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Aranda Carmen¹²³⁴,Ullrich René⁵⁶⁷⁸,Kiebist Jan⁹¹⁰⁸,Scheibner Katrin⁹¹⁰⁸,del Río José C.¹²³⁴^ORCID,Hofrichter Martin⁵⁶⁷⁸,Martínez Angel T.¹¹²¹²⁴^ORCID,Gutiérrez Ana¹²³⁴^ORCID

Affiliation:

1. Instituto de Recursos Naturales y Agrobiología de Sevilla

2. CSIC

3. E-41012 Seville

4. Spain

5. Department of Bio- and Environmental Sciences

6. TU Dresden

7. 02763 Zittau

8. Germany

9. JenaBios GmbH

10. 07749 Jena

11. Centro de Investigaciones Biológicas

12. E-28040 Madrid

Abstract

Different unspecific peroxygenases (UPOs) catalyze the hydroxylation or epoxidation of trans-stilbene and other stilbenoids yielding resveratrol analogs and other compounds.

Funder

Ministerio de Economía y Competitividad

Horizon 2020 Framework Programme

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CY/C8CY00272J

Reference34 articles.

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2. Specific Structural Determinants Are Responsible for the Antioxidant Activity and the Cell Cycle Effects of Resveratrol