Electrochemical late-stage functionalization
Late-stage functionalization (LSF) constitutes a powerful strategy for the assembly or
diversification of novel molecular entities with improved physicochemical or biological …
diversification of novel molecular entities with improved physicochemical or biological …
Green chemistry meets medicinal chemistry: a perspective on modern metal-free late-stage functionalization reactions
The progress of drug discovery and development is paced by milestones reached in organic
synthesis. In the last decade, the advent of late-stage functionalization (LSF) reactions has …
synthesis. In the last decade, the advent of late-stage functionalization (LSF) reactions has …
TEMPO-enabled electrochemical enantioselective oxidative coupling of secondary acyclic amines with ketones
ZH Wang, PS Gao, X Wang, JQ Gao… - Journal of the …, 2021 - ACS Publications
An electrochemical asymmetric coupling of secondary acyclic amines with ketones via a
Shono-type oxidation has been described, affording the corresponding amino acid …
Shono-type oxidation has been described, affording the corresponding amino acid …
Electrochemical NiH‐Catalyzed C(sp3)−C(sp3) Coupling of Alkyl Halides and Alkyl Alkenes
P Li, G Kou, T Feng, M Wang… - Angewandte Chemie …, 2023 - Wiley Online Library
Herein, an electrochemically driven NiH‐catalyzed reductive coupling of alkyl halides and
alkyl alkenes for the construction of Csp3− Csp3 bonds is firstly reported. Notably, alkyl …
alkyl alkenes for the construction of Csp3− Csp3 bonds is firstly reported. Notably, alkyl …
Electrochemistry for the chemoselective modification of peptides and proteins
Although electrochemical strategies for small-molecule synthesis are flourishing, this
technology has yet to be fully exploited for the mild and chemoselective modification of …
technology has yet to be fully exploited for the mild and chemoselective modification of …
Electrochemical oxidative C(sp3)–H cross-coupling with hydrogen evolution
Abstract Oxidative C (sp 3)–H bond functionalization is a powerful tool in organic synthesis,
but the stoichiometric oxidants required for bond formation raise environmental concerns …
but the stoichiometric oxidants required for bond formation raise environmental concerns …
Convergent Synthesis of 1,4-Dicarbonyl Z-Alkenes through Three-Component Coupling of Alkynes, α-Diazo Sulfonium Triflate, and Water
X Wang, WY Tong, B Huang, S Cao, Y Li… - Journal of the …, 2022 - ACS Publications
We report a general protocol for the convergent synthesis of 1, 4-dicarbonyl Z-alkenes form
alkynes using α-diazo sulfonium triflate and water. The C═ O, C═ C, and C–H bonds are …
alkynes using α-diazo sulfonium triflate and water. The C═ O, C═ C, and C–H bonds are …
Photoinduced Chemo‐, Site‐ and Stereoselective α‐C(sp3)−H Functionalization of Sulfides
Z Tan, S Zhu, Y Liu, X Feng - Angewandte Chemie, 2022 - Wiley Online Library
The ubiquity of sulfur‐containing molecules in biologically active natural products and
pharmaceuticals has long attracted synthetic chemists to develop efficient strategies towards …
pharmaceuticals has long attracted synthetic chemists to develop efficient strategies towards …
Advances in organic electrochemical synthesis
W Zhenhua, M Cong, F **, X Haichao… - Acta Chimica …, 2022 - sioc-journal.cn
摘要 有机电化学合成已成为一种实用, 环境友好的合成方法, 广泛应用于氧化,
还原以及氧化还原中性反应. 通过精准调控电流或者电位可在温和反应条件下实现一些具有挑战 …
还原以及氧化还原中性反应. 通过精准调控电流或者电位可在温和反应条件下实现一些具有挑战 …
Divergent Acyl and Decarbonylative Liebeskind–Srogl Cross-Coupling of Thioesters by Cu-Cofactor and Pd–NHC (NHC= N-Heterocyclic Carbene) Catalysis
Transition-metal-catalyzed cross-coupling reactions of thioesters by selective acyl C (O)–S
cleavage have emerged as a powerful platform for the preparation of complex molecules …
cleavage have emerged as a powerful platform for the preparation of complex molecules …