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 …
modern synthetic organic chemistry, often affording unprecedented reactivity. The …
Recent development of aryl diazonium chemistry for the derivatization of aromatic compounds
F Mo, D Qiu, L Zhang, J Wang - Chemical Reviews, 2021 - ACS Publications
Aryl diazonium salts are versatile building blocks in organic synthesis. In light of the ever-
increasing importance of aryl diazonium salts spanning most disciplines of the chemical …
increasing importance of aryl diazonium salts spanning most disciplines of the chemical …
Methodologies and strategies for selective borylation of C–Het and C–C bonds
M Wang, Z Shi - Chemical Reviews, 2020 - ACS Publications
Organoborons have emerged as versatile building blocks in organic synthesis to achieve
molecular diversity and as carboxylic acid bioisosteres with broad applicability in drug …
molecular diversity and as carboxylic acid bioisosteres with broad applicability in drug …
Diboron (4) compounds: from structural curiosity to synthetic workhorse
Although known for over 90 years, only in the past two decades has the chemistry of diboron
(4) compounds been extensively explored. Many interesting structural features and reaction …
(4) compounds been extensively explored. Many interesting structural features and reaction …
Selection of boron reagents for Suzuki–Miyaura coupling
AJJ Lennox, GC Lloyd-Jones - Chemical Society Reviews, 2014 - pubs.rsc.org
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 …
catalysed carbon–carbon bond forming reaction to date. Its success originates from a …
[图书][B] New trends in cross-coupling: theory and applications
TJ Colacot - 2014 - books.google.com
Palladium-catalysed cross-coupling reactions constitute a powerful class of chemical
methods for the creation of carbon-carbon and carbon-heteroatom bonds used in organic …
methods for the creation of carbon-carbon and carbon-heteroatom bonds used in organic …
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
Y Cheng, C Mück‐Lichtenfeld, A Studer - Angewandte Chemie, 2018 - Wiley Online Library
A metal‐free radical borylation of alkyl and aryl iodides with bis (catecholato) diboron
(B2cat2) as the boron source under mild conditions is introduced. The borylation reaction is …
(B2cat2) as the boron source under mild conditions is introduced. The borylation reaction is …
Scalable, metal-and additive-free, photoinduced borylation of haloarenes and quaternary arylammonium salts
We report herein a simple, metal-and additive-free, photoinduced borylation of haloarenes,
including electron-rich fluoroarenes, as well as arylammonium salts directly to boronic acids …
including electron-rich fluoroarenes, as well as arylammonium salts directly to boronic acids …
sp 2–sp 3 diboranes: astounding structural variability and mild sources of nucleophilic boron for organic synthesis
RD Dewhurst, EC Neeve, H Braunschweig… - Chemical …, 2015 - pubs.rsc.org
Despite the widespread use of organoborane reagents in organic synthesis and catalysis, a
major challenge still remains: very few boron-centered nucleophiles exist for the direct …
major challenge still remains: very few boron-centered nucleophiles exist for the direct …
Pyridine-catalyzed radical borylation of aryl halides
L Zhang, L Jiao - Journal of the American Chemical Society, 2017 - ACS Publications
A pyridine-catalyzed transition-metal-free borylation reaction of haloarenes has been
developed based on the selective cross-coupling of an aryl radical and a pyridine-stabilized …
developed based on the selective cross-coupling of an aryl radical and a pyridine-stabilized …