Compound 3a showed excellent herbicidal activity against barnyard grass with IC ₅₀ = 7.0 mg L ⁻¹ , and exhibited good selection for rice, wheat, and radish at 100 mg L ⁻¹ .

Rosin is an important forestry resource with a specific three-membered phenanthrene ring structure, which can improve the mechanical resistance of polymer coatings. In this paper, a high purity rosin monomer, tri-allyl maleopimarate containing three allyl groups has been synthesized. The yield of the monomer product was 93.2% with the purity of 96.1%. The structure of the synthesized monomer was characterized through gas chromatography (GC), mass spectrometry (MS), hydrogen nuclear magnetic resonance spectroscopy (¹H NMR), carbon nuclear magnetic resonance spectroscopy (¹³C NMR) and elemental analysis. Additionally, we present new experimental results regarding the polymerization reaction under ultraviolet (UV) irradiation. The cured film of tri-allyl maleopimarate exhibited good mechanical properties. The films were also characterized through thermogravimetric (TG) and differential scanning calorimetry (DSC) analyses and a mechanism for polymerization was proposed. Overall, a facile catalytic process for the valorization of rosin in the field of UV polymerization is reported.

In this study, a series of novel sec-p-menthane-7-amine derivatives were designed, synthesized, and evaluated to be used as efficient botanical herbicides owing to their post-emergence herbicidal activities against barnyard grass and rape.

Pyridine acylhydrazone derivatives of isopimaric acid were synthesized and characterized. The minimum inhibitory concentrations of the compounds against five bacteria were determined and most of the compounds displayed some degree of antibacterial activity. The results showed that antimicrobial activity against Streptococcus pneumoniae improved when halogen atoms were introduced into the isopimaric acid, especially when one bromine atom was introduced in the para-position of isopimaric acid. Compound isopimaric acid (5-bromo pyridine-2-formaldehyde) acylhydrazone exhibited a significant antitumorial activity against hepatocarcioma cells (HepG-2) and breast cancer cells (MDA-MB-231), with inhibition degrees of 74.21% and 70.39%, respectively, at 100 μM.