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Hyoungsu, K., Ceshea, M.W., Yongho, P. and Jiyong, H (2007) Stereoselective Synthesis of Tetrahydrofuran Lignans via BF3·OEt2-Promoted Reductive Deoxygenation/Epimerization of Cyclic Hemiketal: Synthesis of (?)-Odoratisol C, (?)-Futokadsurin A, (?)-Veraguensin, (+)-Fragransin A2, (+)-Galbelgin, and (+)-Talaumidin. Organic Letters, 9, 3965-3968.
https://doi.org/10.1021/ol7016388
has been cited by the following article:
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TITLE:
Phyto-Fungicides: Structure Activity Relationships of the Thymol Derivatives against Rhizoctonia solani
AUTHORS:
Kamlesh R. Chauhan, Thanh C. Le, Praveen Kumar Chintakunta, Dilip K. Lakshman
KEYWORDS:
Fungicide, Thymol Derivatives, Rhizoctonia solani
JOURNAL NAME:
Journal of Agricultural Chemistry and Environment,
Vol.6 No.4,
November
9,
2017
ABSTRACT: Thymol, the key component of the thyme oil and its derivatives were evaluated for their structure activity relationship as fungicide against Rhizoctonia solani. Since plant-based chemicals are considered as “Generally Recognized as Safe” (GRAS) chemicals, there is great potential to use those and synthetic derivatives against R. solani and other fungal pathogens, in vitro, and in thegreenhouse or field conditions. Among the six thymol derivatives evaluated, thymol acetate was considered as the most suitable commercially viable plant-based fungicide due to its superior efficacy as well as lowest residue.