Bulky triarylamines can be efficiently made by Buchwald–Hartwig amination with Pd–PEPPSI catalysts

Bifunctional and C2-symmetrical zinc catalysts for the hydrophosphonylation of aldehydes

The hard work is finally complete: Your manuscript is accepted and it’s time to inject a little fun by making a cover picture for your chosen journal

Diols which are conformationaly favorable are specifically activated by LiCl

Spin-center transfer is modified by solvent and temperature in a neutral radical system

The iodoaldol reaction of internal alkynyl ketones gives useful oxygen-functionalized vinyl iodides

Inexpensive hydrochloric acid is promising for low-cost electrochemical chlorination

Organic bis(trifluoromethanesulfonyl)methyl-based catalysts prove versatile for selecting aldol or olefination products

Magnesium/BINOL supramolecular catalysts made for phosphorus addition, Mannich-type, and hetero Diels-Alder reactions

The 3-hydroxy group is the key to controlling cycloaddition reactions of 3-hydroxycyclobutanone