Skip to main content

Journal articles made easy: Natural product herbicide, thaxtomin A


This article looks at developing a natural product herbicide, thaxtomin A. It will help you understand the research the journal article is based on, and how to read and understand journal articles. The research article was originally published in our Organic & Biomolecular Chemistry journal.

Type of Activity

working independently



Age Group

Undergraduate to Teacher

Natural product herbicide (±)-thaxtomin A

A one-pot multicomponent coupling/cyclization for natural product herbicide (±)-thaxtomin 

Click here for the full article in the journal of Organic & Biomolecular Chemistry

Authors: Jean Paul Bourgault, Amarendar Reddy Maddirala and Peter R. Andreana

Why is this study important?

The use of herbicides in the years following World War II has proven to be more effective and less costly than hand removal or tillage for weed control. Furthermore, it is estimated that if these chemicals were discontinued the annual U.S. crop production would decrease by 20%.1 The necessary control of unwanted foliage has been a tale of two stories; on one hand there is the constant threat of herbicide resistance and on the other there are concerns regarding environmental effects.2

Naturally occurring thaxtomin A (TA, syn-1) was first isolated in 1989 from Streptomyces scabies3, the soil bacteria responsible for common scab disease of potatoes, and has since attracted considerable attention from industrial4 and academic5 communities as the molecule responsible for scab infections of potatoes and additionally as a potent phytotoxin demonstrating activity similar to known cellulose inhibitors. TA has also been used to control weed growth and germination in the presence of grasses and cereals causing no toxicity to these crops.4a

This interest is highly motivated by the environmentally benign and biodegradable properties of TA, which contains a cyclic dipeptide or 2,5-diketopiperazine (DKP) core, composed of a (S)-N-methyl-4-nitrotryptophan and (R)-2-hydroxy-3-(3-hydroxyphenyl)-N-methylalanine (Fig. 1). In spite of this attention there exists only a single report on the preparation of thaxtomin A,6 so we expanded on this methodology using the Ugi reaction as an alternative approach for the rapid assembly of the hydroxy DKP TA.

Further information

What is the objective?

The authors' aim was to develop a one pot synthesis of TA using the Ugi reaction for the preparation of an acyclic dipeptide which could then undergo a base mediated amide-ketone cyclization to the desired diketopiperazine (DKP).

What was their overall plan?

This analysis is based on the general mechanism for the Ugi reaction as seen below, Fig 4. A close examination of this reaction process allowed for the correct selection of starting materials required for the formation of 2. By following the color coded starting materials through this mechanism it can be seen how the authors arrived at 3, 4, 5, and 6

  • Search the literature for previous reports on the preparation of 3, 5, and 6 or derivatives thereof. Methyl amine (4) is inexpensive through commercial sources.

  • Prepare the starting materials based on these reports. This is not always possible but in this case all of the precursors or very similar derivatives were already known.

What was their procedure?

To begin, the authors prepared 4-nitroindolacetaldehyde (3) which involved a slight modification of previous reports.7 Initial work on this aldehyde commenced with the preparation of mannich derivative (9), through treatment of 4-nitroindole (7) with bis(dimethylamino)methane (8). This reaction successfully introduced one -CH2- at the 3-postion of the indole. Next dimethyl amine was replaced with a cyano(-CN) group by treatment with KCN affording cyano derivative 10. This transformation installed the second carbon on 3 which will eventually become the aldehyde carbonyl carbon. Cyano 10 then underwent acidic hydrolysis to the carboxylic acid followed by Fischer esterification with sulfuric acid and ethanol to provide ester 11. The ester was then reduced with diisobutylaluminium hydride (DIBALH) to the primary alcohol which was finally oxidized to aldehyde (3), with the hypervalent iodine compound 2-iodoxybenzoic acid (IBX), Scheme 1. 

The authors next prepared 3-hydroxyphenylpyruvic acid (5) as previously described.8 The first step in this sequence involved the reaction of 3-hyroxybenzaldehyde (13) with N-acetylglycine (14) in the presence of acetic anhydride to afford the oxazolone derivative (15). Intermediate 15 then underwent acidic hydrolysis with 3M HCl to the required alpha-ketocarboxylic acid 5, Scheme 2. The key aspect to this starting material is the location of the ketone functional group alpha which is adjacent to the carboxylic acid. The presence of the ketone provides the electrophile and the hydroxyl for the final hydroxy DKP formation, see Fig. 2.

Scheme 2

The final starting material that needed to be prepared (methyl amine, 4, is inexpensive through commercial sources) was methylisocyanide (6). This foul smelling liquid was prepared through dropwise addition of N-methylformamide (16) to p-toluenesulfonyl chloride (TsCl) dissolved in quinoline.9 The newly formed isocyanide was then simultaneously removed from the reaction mixture through vacuum distillation, Scheme 3. 

With all of the required starting materials readily available the authors then conducted the all important Ugi reaction. This multicomponent coupling cascade began with the condensation of methyl amine 4 and aldehyde 12 to form imine 17. After 5 minutes isocyanide 6 and alpha-ketoacid 5 were added sequentially to the reaction mixture, which was then allowed to stir overnight at room temperature. This sequence successfully provided the desired Ugi product (2) in 37% yield. Acyclic 2 was then treated with NEt3 which provided undesired anti-1, however this compound could be converted to thaxtomin A (TA) through treatment with KOH at 70 oC, additionally 2 could be cyclized directed to TA using identical conditions, Scheme 4. 

These successful step wise strategies encouraged the attempt of a one pot conversion of 3, 4, 5, and 6 to TA. In this approach the Ugi reaction was conducted as before with the addition of a cyclization step (KOH, 70 oC) after the Ugi had taken place. This tandem Ugi/cyclization sequence provided a 32% yield of TA as well as an 8% yield of anti-1, Scheme 5. 

What are the conclusions?

4-nitroindolylacetaldehyde (3), methylamine (4), 3-hydroxyphenylpyruvic acid (5) and methyl isocyanide (6) were used in a tandem one-pot Ugi/DKP cyclization process for the natural product thaxtomin A. While this synthesis is inherently limited by the Ugi reaction itself in that only racemic TA is obtained, it clearly demonstrates the power of multicomponent reactions to generate biologically validated scaffolds. Including those embedded in naturally occurring products, in a limited number of synthetic steps in the absence of protecting groups.

What are the next steps?

The authors plan to use the Ugi/cylization sequence described to prepare a library of hydroxy DKP derivatives which will be studied as potential herbicides.  


Journal articles made easy are journal articles from a range of Royal Society of Chemistry journals that have been re-written into a standard, accessible format. They contain links to ChemSpider entries, related journal articles, books and Learn Chemistry resources such as videos of techniques, and resources on theory and activities. They should facilitate students understanding of scientific journal articles and how to extract and interpret the information in them.