The versatility of boron in biological target engagement
DB Diaz, AK Yudin - Nature Chemistry, 2017 - nature.com
Boron-containing molecules have been extensively used for the purposes of chemical
sensing, biological probe development and drug discovery. Due to boron's empty p orbital, it …
sensing, biological probe development and drug discovery. Due to boron's empty p orbital, it …
α-Aminoboronates: recent advances in their preparation and synthetic applications
W Ming, HS Soor, X Liu, A Trofimova… - Chemical Society …, 2021 - pubs.rsc.org
α-Aminoboronic acids and their derivatives are useful as bioactive agents. Thus far, three
compounds containing an α-aminoboronate motif have been approved by the Food and …
compounds containing an α-aminoboronate motif have been approved by the Food and …
Remote Stereocenter through Amide-Directed, Rhodium-Catalyzed Enantioselective Hydroboration of Unactivated Internal Alkenes
Despite the frequent occurrence of γ-branched amines in bioactive molecules, the direct
catalytic asymmetric synthesis of this structural motif containing a remote stereocenter …
catalytic asymmetric synthesis of this structural motif containing a remote stereocenter …
Rhodium-catalyzed regiodivergent and enantioselective hydroboration of enamides
XY Bai, W Zhao, X Sun, BJ Li - Journal of the American Chemical …, 2019 - ACS Publications
Chiral α-and β-aminoboronic acids exhibit unique biological activities. General methods for
the synthesis of these bioisosteres of amino acids are highly desirable. We report a facile …
the synthesis of these bioisosteres of amino acids are highly desirable. We report a facile …
Peptide macrocyclization inspired by non-ribosomal imine natural products
A thermodynamic approach to peptide macrocyclization inspired by the cyclization of non-
ribosomal peptide aldehydes is presented. The method provides access to structurally …
ribosomal peptide aldehydes is presented. The method provides access to structurally …
Boryl-Dictated Site-Selective Intermolecular Allylic and Propargylic C–H Amination
Y Liu, ZH Chen, Y Li, J Qian, Q Li… - Journal of the American …, 2022 - ACS Publications
For internal alkenes possessing two or more sets of electronically and sterically similar
allylic protons, the site-selectivity for allylic C–H functionalization is fundamentally …
allylic protons, the site-selectivity for allylic C–H functionalization is fundamentally …
Regioselective radical borylation of α, β-unsaturated esters and related compounds by visible light irradiation with an organic photocatalyst
Radical hydroboration reactions have only recently been reported and are still rare. Here we
describe a photoredox radical hydroboration of α, β-unsaturated esters, amides, ketones …
describe a photoredox radical hydroboration of α, β-unsaturated esters, amides, ketones …
Metal-catalyzed B–H acylmethylation of pyridylcarboranes: access to carborane-fused indoliziniums and quinoliziniums
HJ Cao, X Wei, F Sun, X Zhang, C Lu, H Yan - Chemical Science, 2021 - pubs.rsc.org
Metal-catalyzed mono-acylmethylation of pyridylcarboranes has been realized using α-
carbonyl sulfoxonium ylides as a coupling partner. The reaction features high efficiency …
carbonyl sulfoxonium ylides as a coupling partner. The reaction features high efficiency …
Recent advances in the synthesis and reactivity of MIDA boronates
Organoboron compounds have a wide-range of applications in synthetic methodologies,
natural products, and bioactive molecule synthesis. The sensitivity of boronic acid toward …
natural products, and bioactive molecule synthesis. The sensitivity of boronic acid toward …
A Versatile Route to Acyl (MIDA) boronates
H Qiao, J Michalland, Q Huang… - Chemistry–A European …, 2023 - Wiley Online Library
A modular approach to highly functional acyl (MIDA) boronates is described. It involves the
generation of the hitherto unknown radical derived from acetyl (MIDA) boronate and its …
generation of the hitherto unknown radical derived from acetyl (MIDA) boronate and its …