The transition metal-catalysed hydroboration reaction

SJ Geier, CM Vogels, JA Melanson… - Chemical Society …, 2022 - pubs.rsc.org
The use of transition metals to catalyse the addition of hydridoboranes to unsaturated
organic molecules was initially realised several decades ago. Although this area of …

First-row d-block element-catalyzed carbon–boron bond formation and related processes

SK Bose, L Mao, L Kuehn, U Radius… - Chemical …, 2021 - ACS Publications
Organoboron reagents represent a unique class of compounds because of their utility in
modern synthetic organic chemistry, often affording unprecedented reactivity. The …

Photoinduced borylation for the synthesis of organoboron compounds: focus review

YM Tian, XN Guo, H Braunschweig, U Radius… - Chemical …, 2021 - ACS Publications
Organoboron compounds have important synthetic value and can be applied in numerous
transformations. The development of practical and convenient ways to synthesize boronate …

N-Heterocyclic carbenes as privileged ligands for nickel-catalysed alkene functionalisation

BC Lee, CF Liu, LQH Lin, KZ Yap, NX Song… - Chemical Society …, 2023 - pubs.rsc.org
Alkene functionalisation is a powerful strategy that has enabled access to a wide array of
compounds including valuable pharmaceuticals and agrochemicals. The reactivity of the …

Replacement of less-preferred dipolar aprotic and ethereal solvents in synthetic organic chemistry with more sustainable alternatives

A Jordan, CGJ Hall, LR Thorp, HF Sneddon - Chemical reviews, 2022 - ACS Publications
Dipolar aprotic and ethereal solvents comprise just over 40% of all organic solvents utilized
in synthetic organic, medicinal, and process chemistry. Unfortunately, many of the common …

Metal-catalyzed Markovnikov-type selective hydrofunctionalization of terminal alkynes

J Chen, WT Wei, Z Li, Z Lu - Chemical Society Reviews, 2024 - pubs.rsc.org
Metal-catalyzed highly Markovnikov-type selective hydrofunctionalization of terminal alkynes
provides a straightforward and atom-economical route to access 1, 1-disubstituted alkenes …

Three-component olefin dicarbofunctionalization enabled by nickel/photoredox dual catalysis

MW Campbell, JS Compton, CB Kelly… - Journal of the …, 2019 - ACS Publications
An intermolecular, photocatalytic dicarbofunctionalization (DCF) of olefins enabled by the
merger of Giese-type addition with Ni/photoredox dual catalysis has been realized …

Synthesis of axially chiral alkenylboronates through combined copper-and palladium-catalysed atroposelective arylboration of alkynes

W Li, S Chen, J Xie, Z Fan, K Yang, Q Song - Nature Synthesis, 2023 - nature.com
The incorporation of alkenylboronates into axially chiral compounds increases their
structural diversity and provides a synthetic handle for late-stage functionalizations. Despite …

Design of hemilabile N, N, N-ligands in copper-catalyzed enantioconvergent radical cross-coupling of benzyl/propargyl halides with alkenylboronate esters

PF Wang, J Yu, KX Guo, SP Jiang… - Journal of the …, 2022 - ACS Publications
The enantioconvergent radical C (sp3)–C (sp2) cross-coupling of alkyl halides with
alkenylboronate esters is an appealing tool in the assembly of synthetically valuable …

Boron-Wittig olefination with gem-bis (boryl) alkanes

AB Cuenca, E Fernández - Chemical Society Reviews, 2021 - pubs.rsc.org
The condensation of easy manageable lithium α-bis (boryl) carbanions with carbonyl
derivatives, the so-called boron-Wittig reaction, allows for the straightforward and often …