Chemoselective reaction of cyanoacetic acid with benzal-4-acetylanilines and fungitoxicity of products
Anjali Sidhu J R Sharma Mangat Rai
Click here to view fulltext PDF
Permanent link:
https://www.ias.ac.in/article/fulltext/jcsc/121/04/0449-0453
Cyanoacetic acid reacted chemoselectively with carbon-nitrogen double bond of benzal-4-acetylaniliines, leaving the carbon-oxygen double bond, considered to be more reactive, intact, leading to the formation of mono addition-elimination products rather than bis attack at both the reactive centres, even when the reaction was carried out with two moles of cyanoacetic acid. The product viz. benzalcyanoacetic acid and its derivatives were screened for their fungitoxicity against five pathogenic fungi.
Anjali Sidhu1 J R Sharma1 Mangat Rai1
Volume 135, 2023
All articles
Continuous Article Publishing mode
Click here for Editorial Note on CAP Mode
© 2022-2023 Indian Academy of Sciences, Bengaluru.