Tag: Organic Chemistry

Trifluoromethyl copper complexes were repurposed for saccharide difluoromethylation
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in ChemistryPhoto- and acid-mediated repurposing of Grushin’s reagent enables efficient difluoromethylation of alcohols, saccharides, and bioactive molecules, generating antifungal leads.

Organic-dye CDC method adds fluoronitromethane to tetrahydroisoquinolines
Organocatalytic cross-dehydrogenative coupling of tetrahydroisoquinolines with fluoronitromethane using Rose Bengal and green LED irradiation for sustainable fluorinated compound synthesis.

Desymmetrization method forms N–N atropisomers with multiple stereocenters
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Asymmetric Michael addition constructs N-N atropisomers from indole-derived maleimides with simultaneous generation of multiple stereocenters, achieving 99% yield and exceptional stereoselectivity.

Trans-decalin moiety of pyrroindomycins constructed
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in ChemistryResearchers achieve synthesis of the decalin core of pyrroindomycin natural products, enabling full structural determination and biosynthetic pathway elucidation.

Three-layer strategy produces fused hydantoins and diketopiperazines
A scalable three-layer synthesis strategy rapidly produces thiazolo-hydantoins and diketopiperazines in under 3 hours without chromatography, enabling one-pot processing and late-stage modification.

New sulfanyl indeno triazinones were synthesized and some cyclized further
Novel one-pot synthesis of 3-alkenyl(propargyl)sulfanyl-indeno[1,2-e][1,2,4]triazin-9-ones with selective heterocyclization through halogenation.

Photocatalysis enabled synthesis of trifluoromethyl amidines and imidates
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in ChemistryPhotocatalytic metal-free synthesis of α-trifluoromethyl amidines and imidates using isocyanides and trifluoroacetylsilanes, with mechanistic insights from DFT studies.

Measured pKa values of triorganophosphonium P–H bonds in toluene
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in ChemistryExperimental pKa values of P-H bonds in triorganophosphonium bistriflimides determined in toluene using spectroscopy and DFT, providing guidelines for catalytic phosphine generation.

Electron-withdrawing groups enable thio-Belluš–Claisen rearrangement with difluoroketene
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in ChemistryNew protocol for thio-Belluš-Claisen rearrangement with difluoroketene using desilylative β-elimination. Electronic effects on substrate promotion of reactivity.










