Transition metal–catalyzed remote C─ H borylation: An emerging synthetic tool

MMM Hassan, S Guria, S Dey, J Das… - Science …, 2023 - science.org
Transition metal–catalyzed C─ H bond activation and borylation is a powerful synthetic
method that offers versatile synthetic transformation from organoboron compounds to …

Transition-metal-catalyzed silylation and borylation of C–H bonds for the synthesis and functionalization of complex molecules

IF Yu, JW Wilson, JF Hartwig - Chemical Reviews, 2023 - ACS Publications
The functionalization of C–H bonds in organic molecules containing functional groups has
been one of the holy grails of catalysis. One synthetically important approach to the diverse …

CH Borylation: A Toolbox for Molecular Diversification

S Guria, MMM Hassan, B Chattopadhyay - Organic Chemistry …, 2024 - pubs.rsc.org
Iridium-catalyzed C–H activation and borylation has become as a powerful synthetic tool in
the past few decades because of the widespread applicability and versatility of organoboron …

Interrogating the Crucial Interactions at Play in the Chiral Cation-Directed Enantioselective Borylation of Arenes

K Ermanis, DC Gibson, GR Genov, RJ Phipps - ACS catalysis, 2023 - ACS Publications
Rendering a common ligand scaffold anionic and then pairing it with a chiral cation
represents an alternative strategy for developing enantioselective versions of challenging …

Visible-light-mediated ruthenium-catalyzed para-selective alkylation of unprotected anilines

X Lv, Y Cheng, Y Zong, Q Wang, G An, J Wang… - ACS Catalysis, 2023 - ACS Publications
Anilines are important moieties in organic chemistry, pharmaceuticals, and materials
science. Although para-selective functionalization of anilides and tertiary anilines is well …

C–H Borylation of Benzophenones Using Hydrazone as the Traceless Directing Group

Z Yang, L Hao, X Xu, Y Wang, G Wu, Y Ji - Organic Letters, 2023 - ACS Publications
C–H borylation is one of the powerful C–H bond functionalization reactions. In this context, a
metal-free C–H borylation of benzophenones using hydrazone as the traceless directing …

Diversification of Aryl Sulfonyl Compounds through Ligand‐Controlled meta‐ and para‐C−H Borylation

Y Wang, W Chang, S Qin, H Ang, J Ma… - Angewandte Chemie …, 2022 - Wiley Online Library
Aryl sulfones and aryl sulfonamides are of great importance in organic synthesis and
medicinal chemistry. Although ortho‐C− H functionalization of aryl sulfonyl compounds has …

Ligand- and Substrate-Controlled para C–H Borylation of Anilines at Room Temperature

C Haldar, R Bisht, J Chaturvedi, S Guria… - Organic …, 2022 - ACS Publications
A new catalytic method for para borylation of unprotected anilines is described. The catalytic
method is developed by designing a new type of ligand framework that enables para …

Nickel-Catalyzed Site-Selective C3–H Functionalization of Quinolines with Electrophilic Reagents at Room Temperature

X Sheng, M Yan, B Zhang, WY Wong, N Kambe… - ACS …, 2023 - ACS Publications
Herein, we disclose a mild and versatile nickel-catalyzed method for exclusive C3-selective
thioetherification, alkylation, arylation, acylation, and phosphorylation of quinolines with a …

Noncovalent interaction with a spirobipyridine ligand enables efficient iridium-catalyzed C–H activation

Y Jin, B Ramadoss, S Asako, L Ilies - Nature Communications, 2024 - nature.com
Exploitation of noncovalent interactions for recognition of an organic substrate has received
much attention for the design of metal catalysts in organic synthesis. The CH–π interaction is …