Synthesis, Fungitoxicity and Quantitative Structure-Activity Relationship of O-Aryl O-2-Chloroethyl O-Ethyl Phosphates. -Nineteen new organophosphates are synthesized and tested for their fungicidal activity. The phosphate (IVe) shows highest activity against the fungi tested and possesses better a
Synthesis and fungicidal activity of O-alkyl O-aryl O-2-(stearamido)ethyl phosphates
✍ Scribed by Liang Han; Jian-Rong Gao; Zheng-Ming Li
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 126 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20485
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
N‐stearoylethanolamine (NAE18:0) was reacted with O‐alkyl O‐aryl chlorophosphate and a series of O‐alkyl O‐aryl O‐2‐(stearamido)ethyl phosphates were synthesized to explore their antifungal activity. Compared with parent NAE18:0, title compounds without substitution or with methyl substitution on a benzene ring exhibited improved antifungal activity. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:602–608, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20485
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