Three-component 1, 2-dicarbofunctionalization of alkenes involving alkyl radicals

P Gao, YJ Niu, F Yang, LN Guo, XH Duan - Chemical Communications, 2022 - pubs.rsc.org
1, 2-Dicarbofunctionalization of alkenes represents an appealing strategy for chemical bond
formation in organic synthesis, which could enable the rapid construction of molecular …

Congested C(sp3)-rich architectures enabled by iron-catalysed conjunctive alkylation

TD Tan, JMI Serviano, X Luo, PC Qian, PL Holland… - Nature Catalysis, 2024 - nature.com
Catalytic cross-coupling by transition metals has revolutionized the formation of carbon–
carbon bonds in organic synthesis. However, the challenge of forming multiple alkyl–alkyl …

General method for iron-catalyzed multicomponent radical cascades–cross-couplings

L Liu, MC Aguilera, W Lee, CR Youshaw, ML Neidig… - Science, 2021 - science.org
Transition metal–catalyzed cross-coupling reactions are some of the most widely used
methods in chemical synthesis. However, despite notable advantages of iron (Fe) as a …

Chemoselective union of olefins, organohalides, and redox-active esters enables regioselective alkene dialkylation

T Yang, Y Jiang, Y Luo, JJH Lim, Y Lan… - Journal of the American …, 2020 - ACS Publications
Multicomponent catalytic processes that can generate multiple C (sp3)–C (sp3) bonds in a
single step under mild conditions, particularly those that employ inexpensive catalysts and …

Asymmetric three-component olefin dicarbofunctionalization enabled by photoredox and copper dual catalysis

PZ Wang, Y Gao, J Chen, XD Huan, WJ **ao… - Nature …, 2021 - nature.com
The intermolecular three-component alkene vicinal dicarbofunctionalization (DCF) reaction
allows installation of two different carbon fragments. Despite extensive investigation into its …

General and practical route to diverse 1-(difluoro) alkyl-3-aryl bicyclo [1.1. 1] pentanes enabled by an Fe-catalyzed multicomponent radical cross-coupling reaction

A Rentería-Gómez, W Lee, S Yin, M Davis… - ACS …, 2022 - ACS Publications
Bicyclo [1.1. 1] pentanes (BCPs) are of great interest to the agrochemical, materials, and
pharmaceutical industries. In particular, synthetic methods to access 1, 3-dicarbosubsituted …

Photoinduced 1, 2-dicarbofunctionalization of alkenes with organotrifluoroborate nucleophiles via radical/polar crossover

MJ Cabrera-Afonso, A Sookezian, SO Badir… - Chemical …, 2021 - pubs.rsc.org
Alkene 1, 2-dicarbofunctionalizations are highly sought-after transformations as they enable
a rapid increase of molecular complexity in one synthetic step. Traditionally, these …

Modular and Practical 1, 2‐Aryl (Alkenyl) Heteroatom Functionalization of Alkenes through Iron/Photoredox Dual Catalysis

W Zhang, T Liu, HT Ang, P Luo, Z Lei, X Luo… - Angewandte …, 2023 - Wiley Online Library
Abstract Efficient methods for synthesizing 1, 2‐aryl (alkenyl) heteroatomic cores,
encompassing heteroatoms such as nitrogen, oxygen, sulfur, and halogens, are of …

Chemoselective Cu-catalyzed cross-nucleophile alkylarylation of alkenes

SH Lee, JD Yu, AL Monterde, SE Tung, YN Wang… - ACS …, 2024 - ACS Publications
We report a general cross-nucleophile alkene alkylarylation that adds two different boronic
acids, an alkyl and an aryl, across a vinylarene to afford 1, 1-diarylalkanes. The high …

A free-radical design featuring an intramolecular migration for a synthetically versatile alkyl–(hetero) arylation of simple olefins

DJ Babcock, AJ Wolfram, JL Barney, SM Servagno… - Chemical …, 2024 - pubs.rsc.org
A free-radical approach has enabled the development of a synthetically versatile alkyl–
(hetero) arylation of olefins. Alkyl and (hetero) aryl groups were added concurrently to a full …