All stereochemistry articles
-
ResearchChirality-flipping reaction could completely change total synthesis strategies
Photocatalytic reaction that inverts configuration of chiral carbon centres offers new stereochemical editing logic
-
-
-
ResearchAutomated carbon-13 NMR structure validation program highlights errors atom-by-atom
Introducing a new measure to quantify molecular structural uncertainty
-
WebinarResolving absolute stereochemistry in early drug discovery with VCD
From sample preparation to use of quantum chemical software tools, learn how vibrational circular dichroism (VCD) streamlines chiral analysis in the R&D analytical support lab
-
-
ResearchMachine-learning tool performs stereochemical assignments on SPM images
Identifying chiral centres on SPM images with machine-learning tools only takes a few hours and could save researchers time
-
ResearchNewly discovered marine compound is in a super-carbon-chain league of its own
Isolated from algae, Benthol A has 35 stereocentres
-
ArticleChemistry pedagogy for a modern world
The Royal Society of Chemistry has taken a new approach to teaching higher education students the fundamentals of maths and stereochemistry, putting students themselves at the heart of the process
-
ResearchProgram that automatically interprets NMR spectra is boon for structure elucidation
Raw NMR data takes 60 seconds, rather than eight hours, to go from spectrometer to structure
-
-
ResearchSynthetic strategy exploits fluxional nitrogen to deliver three chiral centres for the price of one
Innovative method amplifies chirality and complexity in medicinally relevant cyclic hydrazines
-
Research‘Inside-out’ chirality discovered by chance could have been missed in many molecules
A structure assignment odyssey finds a natural product with a type of isomerism never before seen in small molecules
-
ResearchExplosive 25% more powerful than TNT found in first study of energetic isomers
Stereo- and regiochemistry affect compounds’ explosive potential
-
ResearchChiral borane complexes catalyse new synthesis opportunities
N-heterocyclic carbene-borane complexes with a rare stereogenic boron centre demonstrate potential in stereoselective catalysis
-
ResearchFlexible catalyst systems open up nitrile chemistry
One new strategy enantioselectively produces amines from nitriles, and another generates valuable alkenyl nitriles
-
ResearchWalking radicals relocate double bonds
Nickel-guided radicals walk along carbon chains to make E-alkenes from terminal alkenes
-
ResearchFlexible route to enantiomerically enriched cyclobutanes
System for modifying square starting molecule could be gateway to numerous bioactive molecules
-
ResearchRound-the-ring catalysis makes cyclic peptides chiral
Classic hydrogenation catalyst installs multiple stereocentres one by one to create small amino acid rings as single enantiomers
-
ResearchFirst new form of isomerism discovered in 50 years will be the last
Porphyrin–boron compounds have revealed a curious form of molecular chirality based on hindered bond angle inversion