Related Experiment Video
Updated: May 10, 2025

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Biocatalyzed Synthesis of Benzoyl and Cinnamoylamides Inspired by Rice Phytoalexins
Cecilia Pinna1, Luca Nespoli1, Giulia Brioschi1
1Department of Food, Environmental and Nutritional Sciences (DeFENS), University of Milan, via Celoria 2, 20133 Milan, Italy.
Abstract:
Worldwide, phytopathogenic fungi, bacteria, and viruses are responsible for huge crop losses each year, threatening agricultural progress and food security and causing massive economic damages. Pyricularia oryzae represents one of the most dangerous fungal phytopathogens being the cause of rice blast, a highly destructive disease widely distributed across the world. In this critical context, good agricultural practices necessarily need to be supported using novel, effective, and sustainable agrochemicals. It is known that plants naturally counteract exogenous infections by synthesizing defense secondary metabolites, known as phytoalexins. Inspired by N-benzoyltryptamine and N-cinnamoyltryptamine, two phytoalexins found in Oryza sativa, we designed a collection of tryptamine-based derivatives. The compounds were synthesized exploiting an enzymatic approach, using Candida antarctica Lipase B (CaL-B) as a biocatalyst and tert-amyl alcohol (t-AA) as an unconventional green solvent. The activity was evaluated against a panel of different phytopathogenic fungi as well as selected Gram-negative and Gram-positive bacteria. The obtained results pave the way for novel nature-inspired products as a valuable alternative to currently available pesticides.
Related Concept Videos
Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condensation
As the self-condensation of ketones is generally not favored in basic conditions, the self-condensed products do not form in the reaction between ketones and benzaldehyde. The general reaction of Claisen–Schmidt...
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is...
Nucleophilic Aromatic Substitution: Elimination–Addition
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism
The reaction begins with the nucleophilic addition between a phosphorus ylide and the carbonyl compound. Due to its carbanionic character, phosphorus ylide acts as a strong nucleophile and attacks the electrophilic carbonyl group. This generates a charge-separated dipolar intermediate called betaine. The negatively charged oxygen...

![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)