Organic chemistry – Page 41
-
ResearchTheory vindicated as infrared laser drives up reaction's speed by 24%
Reaction efficiency could be improved by exploiting vibrational excitation
-
ResearchMolecular box treats chemists to a strained surprise
Introducing pillar[4]pyridinium – the first of a new family of macrocycles
-
ResearchSuper-reducing solvated electrons made with an LED
Laser-free method lowers the cost of producing hydrated electrons
-
OpinionChanging the reproducibility rulebook
It pays to know when taking shortcuts is acceptable, and which it’s safe to take
-
ResearchA light switch for chemical reactions
Different wavelengths of light can flip the route a reaction takes
-
ResearchAI translates chemistry to predict reaction outcomes
Machine learning tool predicts products of organic reactions by treating chemistry like language
-
ResearchTelescope arrangement puts a twist on organic synthesis
Solvents, move aside – scientists achieve dry multicomponent synthesis in a single step with twisting screws
-
ResearchCalcium breaks ‘like repels like’ rule in benzene alkylation
Serendipitous discovery sees main-group metal topple textbook paradigm
-
OpinionBeyond buckets and batches
Embracing flow chemistry means leaving behind some faithful friends
-
ResearchOld and new spectroscopic techniques team up to decipher intricate alkaloids
Cutting-edge strategies set to increase our access to chemical space after researchers use them to verify unprecedented structures
-
ResearchAcene synthesis sets new record for twisted molecules
Chemists prepare ‘twistacenes’ with torsion angles of up to 170º
-
ResearchWhat’s left isn’t always right in total synthesis
Scientists turn detective to solve a decade-old stereochemical enigma
-
ResearchTagging drugs with heavy hydrogen made as easy as flicking a light switch
Photoredox reaction simplifies metabolism studies by swapping hydrogen for deuterium or tritium
-
OpinionThe value of quantification
A skills gap is emerging in organic synthesis that needs to be closed
-
ResearchSpaces can be useful
Truly functional MOFs are on the horizon but Susumu Kitagawa saw their potential when they were weak and idle
-
OpinionNatural selection
Bioactive compounds don’t just inspire new synthetic strategies, they’re also the ultimate test
-
Opinion(‒)-Pavidolide B
An innovative approach to making five-membered carbon rings makes for a strikingly short synthesis
-
ResearchFlash lithiation made safe
Micromixing enables protecting-group-free synthesis of organolithiums
-
WebinarWho says there are no shortcuts to great chemistry?
Now more than ever with ChemDraw® and ChemOffice 17, you can spend less time drawing and more time conducting and capturing your research, whether you are a chemist or a biochemist.
-
ResearchPurple crystals boast first aluminium double bond
Aluminium analogue of an alkene completes series of double-bonded boron group elements