Abstract
AbstractSubstitution of alkyl benzimidazol‐2‐ylcarbamates by phenoxy‐ or phenylthio‐groups in the 5‐position results in an increase in anthelmintic activity. The biological spectrum is altered by substitution of the phenyl ring. A sulphonic ester substituent in the 5‐position of the benzimidazole nucleus also increases anthelmintic activity.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
