1,2,4,5-Tetroxane is a cyclic organic peroxide with a four-membered ring containing two oxygen-oxygen (peroxide) bonds. It's a class of compounds known for their antimalarial activity and has been the subject of research for potential use as a drug.
Tetraoxane candidate development:[13] SAR trends of novel 1,2,4,5-tetraoxanes and candidate selection of RKA182.
Silver triflate is a highly effective catalyst in organic reactions, promoting reactions like Friedel-Crafts reactions, nucleophile-alkene cyclizations, and esterifications. Silver triflate can be prepared from the reaction of trifluoromethanesulfonic acid with silver oxide or silver carbonate.
Scope Investigation for the Silver Triflate-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime 1 with Alkylide-necyclopropane 2
Possible Mechanism for the Silver Triflate-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime 1 with Alkylide-necyclopropane 2
2-Cyclopropen-1-one is a highly strained, three-membered cyclic ketone. As the smallest member of the cyclopropenone family, it consists of a cyclopropene ring bearing a carbonyl group, making it both aromatic and electrophilic.
Photochemical decarbonylation of a cyclopropenone caged BCN probe (photo-DMBO) activates reactivity toward tetrazine-containing proteins, conferring spatial and temporal control over protein labeling.
3-Pyridinyl is a substituted pyridine ring in which a functional group is attached at the third carbon of the six-membered aromatic nitrogen-containing ring. The parent structure, pyridine, is similar to benzene but contains one nitrogen atom replacing a CH group, imparting basicity and unique reactivity. In the 3-pyridinyl configuration (also called meta-pyridyl), the substituent is bonded to the carbon atom adjacent to the nitrogen (but not directly next to it), influencing the molecule's electronic and steric properties. This moiety is commonly found in pharmaceuticals, agrochemicals, and ligands due to its ability to participate in hydrogen bonding, coordination chemistry, and π–π interactions.
Competition curves of naltrexone (◼) and compounds 8 (△), 9 (▼), 10 (+), 12 (▲), 15 (◇), 31 (○) and 32 (●) for [3H]-DAMGO binding to Wistar rat forebrain membranes.
BMS-309403 is a synthetic, cell-permeable, and orally active chemical compound that acts as a potent and selective inhibitor of fatty acid binding protein 4 (FABP4), also known as aP2. It is being researched for its potential in treating conditions like type 2 diabetes and atherosclerosis due to its ability to reduce inflammation and improve insulin sensitivity.
Hydrazine, anhydrous appears as a colorless, fuming oily liquid with an ammonia-like odor. It can cause cancer according to an independent committee of scientific and health experts.
Hydrazine Scope
Modified diamine catalysts were synthesized starting from the commercial chiral diamine 2. All catalysts except 1a and 1k were easily prepared from 2 in a 4-step sequence as shown in Scheme 2.
Regioselective Synthetic Pathway for 1,3-Disubstituted Tetrahydroindazolones Using Hydrazines 1 and 2-(Hydroxy(N-Boc-pyrrolidin-2-yl)methylene)-5,5-dimethylcyclohexane-1,3-dione 3