Regioselective synthesis, isomerisation, in vitro oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers-Reference-Cited by-同舟云学术

Regioselective synthesis, isomerisation, in vitro oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers

Published:2019 Issue:24 Volume:21 Page:6622-6633
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Koelewijn Steven-Friso¹²³⁴⁵^ORCID,Ruijten Dieter¹²³⁴⁵^ORCID,Trullemans Laura¹²³⁴⁵^ORCID,Renders Tom¹²³⁴⁵^ORCID,Van Puyvelde Peter⁶⁷⁸³⁴^ORCID,Witters Hilda⁹¹⁰¹¹¹²⁵^ORCID,Sels Bert F.¹²³⁴⁵^ORCID

Affiliation:

1. Dept. of Microbial and Molecular Systems (M2S)

2. Centre for Sustainable Catalysis and Engineering (CSCE)

3. KU Leuven

4. 3001 Leuven

5. Belgium

6. Dept. of Chemical Engineering

7. Soft Matter

8. Rheology and Technology (SMaRT)

9. Dept. of Health

10. Applied Bio & molecular Systems (ABS)

11. Flemish Institute for Technological Research (VITO)

12. 2400 Mol

Abstract

Biobased ortho-methoxy groups ameliorate classic bisphenol chemistry in terms of synthesis, safety and processing; bisguaiacol F is used as a test case.

Funder

KU Leuven

Interreg

Fonds Wetenschappelijk Onderzoek

Fonds De La Recherche Scientifique - FNRS

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/GC/C9GC02619C

Reference42 articles.