Suzuki–Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal
catalysed carbon–carbon bond forming reaction to date. Its success originates from a …

Non‐racemic chiral boronic esters are recognised as immensely valuable building blocks in
modern organic synthesis. Their stereospecific transformation into a variety of functional …

Amphotericin B (AmB) is a prototypical small molecule natural product that can form ion
channels in living eukaryotic cells and has remained refractory to microbial resistance …

Organoboron compounds have become one of the most versatile building blocks in organic
synthesis owing to their accessible and efficient conversion into many different functional …

This Minireview highlights advances in the Suzuki–Miyaura cross‐coupling of secondary
boron reagents for the creation of C C bonds with control of stereochemistry. It also …

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 …

The Suzuki–Miyaura cross-coupling reaction has emerged as one of the most powerful
methods for the construction of carbon–carbon bonds. Though most widely utilized for the …

Asymmetric cross‐couplings based on 1, 2‐carbon migration from B‐ate complexes have
been developed efficiently to access valuable organoboronates. However, enantioselective …

A copper-catalyzed regio-and enantioselective hydroamination of alkenyl dan boronates
(dan= 1, 8-diaminonaphthyl) with hydrosilanes and hydroxylamines proceeds to deliver the …

This Article describes the development of a base-free, nickel-catalyzed decarbonylative
coupling of carboxylic acid fluorides with diboron reagents to selectively afford aryl boronate …