Heterocyclic analogs of diflubenzuron as growth and reproduction inhibitors of the fall armyworm and house fly

DeMilo, Albert B.; Ostromecky, Diane M.; Chang, Shen Chin; Redfern, R. E.; Fye, Richard L.

doi:10.1021/jf60215a035

Cited by 19 publications

(9 citation statements)

References 8 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…In the area of natural products, cabergoline is a potent dopamine receptor agonist on D 2 receptors . In agriculture, the growth and reproduction of the fall armyworm and house fly could be hampered using some N‐ acylurea . Moreover, N‐Acylureas are important intermediates for synthesis of amides and esters …”

Section: Introductionmentioning

confidence: 99%

Efficient Synthesis of N‐Acylureas Using Copper Oxide Supported on Magnetic Nanoparticles in Deep Eutectic Solvent

et al. 2018

View full text Add to dashboard Cite

A unique combination of deep eutectic solvent (the combination of urea with choline chloride) and magnetic CuO@γ‐Fe2O3 nanoparticles as a green magnetic nanocatalyst promotes the synthesis of N‐acylureas from reaction carbodiimides with carboxylic acids. This reaction gives the corresponding N‐acylurea derivatives in good to high yields. Easy preparation and separation, inexpensive, insensitivity to moisture and reusability of the catalyst are significant features of this method.

show abstract

Section: Introductionmentioning

confidence: 99%

Efficient Synthesis of N‐Acylureas Using Copper Oxide Supported on Magnetic Nanoparticles in Deep Eutectic Solvent

et al. 2018

View full text Add to dashboard Cite

show abstract

“…In addition, N-acylurea derivatives are used as inhibitors of the reproduction and growth for the house fly and fall army worm ( Figure 1). [17] There are various methods to synthesize N-acylurea derivatives from the reactions of carboxylic acids with carbodiimides. [18][19][20] Soeta and Ukaji have reported oxidative coupling reaction of various kind of aldehydes with N,N 0 -disubstituted carbodiimides catalyzed by N-heterocyclic carbene under aerobic conditions to furnish N-acyl derivatives.…”

Section: Introductionmentioning

confidence: 99%

Some reactions of 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido) acetic acids

Dürüst

Karakuş

Kariuki

et al. 2018

Synthetic Communications

View full text Add to dashboard Cite

In situ generated 2,4-diaryl substituted munchnones€ from 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido)acetic acids react with acetic anhydride in the presence of 2-nitromethylene thia-zolidine, which is most likely acting as a base, and unexpectedly undergo a Dakin-West type reaction and a concurrent autoxidation reaction leading to the formation of (E)-1-(N,4-dimethylbenzamido)-1-(4fluorophenyl)prop-1-en-2-yl acetate, 4-substitutedphenyl-N-methyl-N-(4-substitutedbenzoyl) benzamides and p-substituted benzoic acids. In addition, a novel and efficient access to N-acyl urea derivatives is described by the reaction between 2-(4-substitutedphenyl)-2-(Nmethyl-N-4-substitutedbenzamido)acetic acids and cyclohexyl, isopropyl carbodiimides in the presence of a base. The structures of all new products were identified on the basis of NMR and IR spectra, along with X-ray diffraction data and HRMS measurements. ARTICLE HISTORY

show abstract

“…Primary acylureas and N‐phenyl acylureas are two common structural motifs in agrochemicals, and medicinal chemistry . These structural motifs serve as pesticides and insecticides exhibiting significant properties such as anti‐inflammatory, antihypnotic, antitumor,, analgesic, antihelmintic and antifungal (Figure ).…”

Section: Introductionmentioning

confidence: 99%

[Amberlyst-15 - (4Na₂ SO₄ -2H₂ O₂ -NaCl) Adduct]: Direct Access to Synthesize Acylureas via Oxidative Amidation of Aldehyde

et al. 2017

View full text Add to dashboard Cite

A simple, efficient and straightforward approach for the synthesis of N‐acylureas has been demonstrated. Herein, novel method for the first time enables oxidative amidation of aldehydes and urea in presence of enclathrated H2O2 adduct and Amberlyst‐15 as catalyst is reported. Various aromatic, hetero‐aromatic and aliphatic aldehydes undergo oxidative amidation with urea and its analogues in moderate to excellent yields. The significant feature of this work includes metal free conditions, an efficient and neutral anhydrous source of H2O2 as oxidant, commercially available catalyst and recyclability of catalyst over several runs without considerable loss in activity.

show abstract

Heterocyclic analogs of diflubenzuron as growth and reproduction inhibitors of the fall armyworm and house fly

Cited by 19 publications

References 8 publications

Efficient Synthesis of N‐Acylureas Using Copper Oxide Supported on Magnetic Nanoparticles in Deep Eutectic Solvent

Efficient Synthesis of N‐Acylureas Using Copper Oxide Supported on Magnetic Nanoparticles in Deep Eutectic Solvent

Some reactions of 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido) acetic acids

[Amberlyst-15 - (4Na₂ SO₄ -2H₂ O₂ -NaCl) Adduct]: Direct Access to Synthesize Acylureas via Oxidative Amidation of Aldehyde

Contact Info

Product

Resources

About

Heterocyclic analogs of diflubenzuron as growth and reproduction inhibitors of the fall armyworm and house fly

Cited by 19 publications

References 8 publications

Efficient Synthesis of N‐Acylureas Using Copper Oxide Supported on Magnetic Nanoparticles in Deep Eutectic Solvent

Efficient Synthesis of N‐Acylureas Using Copper Oxide Supported on Magnetic Nanoparticles in Deep Eutectic Solvent

Some reactions of 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido) acetic acids

[Amberlyst-15 - (4Na2 SO4 -2H2 O2 -NaCl) Adduct]: Direct Access to Synthesize Acylureas via Oxidative Amidation of Aldehyde

Contact Info

Product

Resources

About

[Amberlyst-15 - (4Na₂ SO₄ -2H₂ O₂ -NaCl) Adduct]: Direct Access to Synthesize Acylureas via Oxidative Amidation of Aldehyde