Suzuki‐Miyaura Coupling Reaction (SMCR) has been extensively used in the total synthesis
of natural products. We underscored these achievements in a report published in …

Today we are poised for a transition from the highly customized crafting of specific molecular
targets by hand to the increasingly general and automated assembly of different types of …

Small molecules have extensive untapped potential to benefit society, but access to this
potential is too often restricted by limitations inherent to the highly customized approach that …

Organoboron compounds have a wide-range of applications in synthetic methodologies,
natural products, and bioactive molecule synthesis. The sensitivity of boronic acid toward …

Sequential and iterative Pd-catalyzed cross-coupling reactions can be performed in which
the order of C–C bond formations can be controlled either by the attenuated leaving groups …

Antilipoperoxidant protein dysfunction is associated with many human diseases, suggesting
that bilayer lipid peroxidation may contribute broadly to pathogenesis. Small molecule …

The mechanism of acetylene bromoboration in neat boron tribromide was studied carefully
by means of experiment and theory. Besides the syn-addition mechanism through a four …

A highly concise strategy for the total synthesis of phenanthroindolizidines was developed.
The one-pot iterative Suzuki–Miyaura reaction of aryl boronic acids with ortho-bromoaryl N …

Derzeit kündigt sich ein Wandel von der manuellen Synthese spezifischer Moleküle, die
über individuell angepasste Routen verläuft, hin zu automatisch zusammenfügten …

In this study, we achieved an eight-step enantioselective synthesis of (−)-lamellodysidine A,
a structurally intriguing sesquiterpene natural product featuring a 5/5/6/6-fused tetracyclic …