Heterocyclic compounds Hibiscus sabdariffa Copper Biorefinery Copper catalysis Synthetic methods Cocrystal 5-c’dipyridines Cytosporone E Partial least squares regression Natural deep eutectic solvents Bifurcaria bifurcata Benzylthiouracil Microalgae Candida albicans Dimorphism Label-free water quantification Anti-migration activity Fish oil Gels Lactams Free fatty acids Cosmetic formulation Multicomponent reactions Multicomponent Reaction Halogen-metal exchange Natural compound Label free water quantification Eaton's reagent Antibacterial activity Imidazo12-bpyridazine Anthelmintic Crystalline polymorphism Phthalides C-C coupling Spirolactams Decarboxylative coupling Anti-inflammatory Alkylidenephthalide Label free water quantification natural deep eutectic solvent Extraction Spirulina Partial least squares regression Attenuated Total Reflectance-infrared spectroscopy Alkyl-glycerolipids Larval migration inhibition Hypertension Iodolactonization Alginate Cyclization Nanocarriers Docking Spirulina Heterocyclic Compounds Cycloaddition Health management Mycobacterium tuberculosis Cassia sieberiana DC 2-a4 Iodo-triazoles Algae Copper Catalysis Antibioresistance Cross-coupling Antibiotic resistance Carboxymethylcellulose Ca2+ current Click chemistry Anti-apicomplexan Natural deep eutectic solvent Dehydrogenative coupling Déhydrogenase Efflux pumps Cytotoxicity Natural phthalide Extraction Antiproliferative activity Gastrointestinal parasite Liaison carbone carbone Carbon carbon bond Ether-lipids Multicomponent reaction Friedel-Crafts Inhibitor Gram negative bacteria Azides Active pharmaceutical ingredient Crystallographic properties Condensed tannins Décarboxylation Heligmosomoides polygyrus bakeri Anti-MRSA Anthelminthic activity Heterocycles Imidazo1 Anthocyanins ITS-2 Mesenteric artery Domini reactions Harmine analogues Crystal structure Attenuated Total Reflectance-infrared spectroscopy -Hydroxybutyrolactams Olefination