All stereoselective articles
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ResearchPEGylated ligands boost speed and selectivity in mechanochemical arylations
Study highlights the power of tailoring ligands to mechanochemical conditions
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ResearchSilver bullet catalyst works magic transforming stable C–H bonds into amines
Method allows for late-stage, stereoselective aminations to drug-like molecules
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ResearchBoron building block assembles tetra-substituted alkenes like Lego
Powerful method offers control of stereochemistry to produce drugs and natural products
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ResearchEnzyme-inspired ligand distinguishes between simple alkyl groups
Designer ligand creates active site-like pocket for asymmetric radical reaction
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Research‘Transformative’ carbonyl cross-metathesis used to synthesise alkenes
Two new catalytic methods can produce a broad range of Z- and E-alkenes with remarkable cross-selectivity, paving the way for more efficient organic syntheses
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ResearchNickel catalyst switches on double stereochemistry in reaction between racemic alkanes
First-of-its-kind reaction creates stereocentres by stitching together racemic nucleophiles and electrophiles
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OpinionStereoselectivity with a twist
Helical ligands amplify solvent chirality to control reaction outcomes
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ResearchNew tools direct reactions at specific C–H bonds in organic molecules
Elegant catalysts offer quicker routes to complex compounds
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ResearchChallenging mirror molecules made with stereochemistry destroying reaction
Clever catalyst repurposes classic nucleophilic substitution to make chiral quaternary carbon centres
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ResearchCatalyst sets sights on C–H sites
New catalyst stereoselectively functionalises unactivated C–H bonds
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ResearchRoute to complex amines holds drug development promise
New catalytic reaction yields products with three adjacent chiral centres
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