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Synthesis and fungicidal activity of O‐alkyl O‐aryl O‐2‐(stearamido)ethyl phosphates

Synthesis and fungicidal activity of O‐alkyl O‐aryl O‐2‐(stearamido)ethyl phosphates 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 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

Synthesis and fungicidal activity of O‐alkyl O‐aryl O‐2‐(stearamido)ethyl phosphates

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References (22)

Publisher
Wiley
Copyright
Copyright © 2008 Wiley Periodicals, Inc.
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.20485
Publisher site
See Article on Publisher Site

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

Journal

Heteroatom ChemistryWiley

Published: Sep 1, 2008

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