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The pineapple leaves (PL) left over in the fields after pineapple harvest or burnt out, generate waste which contributes to the release of greenhouse gases. As pineapple is one of the most harvested crops in the world, the quantity of pineapple trash and its disposal methods are challenging. The composition of PL waste makes it unique to encounter the increasing demand for renewable energy and other useful products. This review is focused on the production of different biorefinery products and miscellaneous products from PL waste. The high cellulose content in PL makes it a potential feedstock for the production of different biorefinery products like bioethanol, oligosaccharides, nitrocellulose, and humic acid apart from this, waste is also useful for the production of different products like pineapple leaf fibres, fake eyelashes, organic leather, pulp and paper. Although the opportunities, future perspectives, and challenges concerning PL waste utilization to value-added goods were also addressed. It has been demonstrated that pineapple waste conversions lower waste creation, and the products produced by the conversion would promote the 'waste-to-wealth' notion. [ABSTRACT FROM AUTHOR]

We report herein the synthesis of ¾ substituted benzene sulfonamides linked via phenyl ring to a benzothiazole moiety. The title compounds in the two series namely N-(4-(benzothiazole-2-yl) phenyl) 4-substituted benzene sulfonamides and N-(4-(benzothiazole-2-yl) phenyl) 3-substituted benzene sulfonamides were synthesized by condensing 2-(3/4-aminophenyl) benzothiazole with various substituted sulfonyl chlorides. The synthesized compounds were subjected to neurotoxicity screening, computational studies, and evaluation of their anticonvulsant potential. Amongst all the synthesized compounds, compound 9 emerged as the most potent anticonvulsant agent in maximal electroshock (MES) model (standard: phenytoin) in mice and showed three hydrogen bond interactions with the nicotinic acetylcholine ion gated receptors (PDB ID: 2BG9). Interestingly, compound 13 showed five hydrogen bond interactions with the target protein and thus excellent binding affinity upon computational analysis but was found to be neurotoxic. [ABSTRACT FROM AUTHOR]