Determining the excited-state substituent constants of furyl and thienyl groups-Reference-Cited by-同舟云学术

Determining the excited-state substituent constants of furyl and thienyl groups

Published:2018-01-09 Issue:5 Volume:31 Page:e3799
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J Phys Org Chem

Author:

Qu Junyan¹,Cao Chao-Tun¹,Cao Chenzhong¹^ORCID

Affiliation:

1. Key Laboratory of Theoretical Organic Chemistry and Function Molecule, Ministry of Education, Key Laboratory of QSAR/QSPR of Hunan Provincial University, School of Chemistry and Chemical Engineering; Hunan University of Science and Technology; Xiangtan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference35 articles.

1. Effects of stilbene components of the roots of Polygonum cuspidatum Sieb. et Zucc. on lipid metabolism.

2. Plant stilbenes induce endoplasmic reticulum stress and their anti-cancer activity can be enhanced by inhibitors of autophagy

3. Lipid-lowering therapy in diabetes mellitus

4. Biosynthesis, metabolism, molecular engineering, and biological functions of stilbene phytoalexins in plants

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