Photons or electrons? A critical comparison of electrochemistry and photoredox catalysis for organic synthesis

NES Tay, D Lehnherr, T Rovis - Chemical reviews, 2021 - ACS Publications
Redox processes are at the heart of synthetic methods that rely on either electrochemistry or
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …

Desulfonylation via radical process: recent developments in organic synthesis

XQ Chu, D Ge, YY Cui, ZL Shen, CJ Li - Chemical reviews, 2021 - ACS Publications
As the “chemical chameleon”, sulfonyl-containing compounds and their variants have been
merged with various types of reactions for the efficient construction of diverse molecular …

Synthetic organic electrochemical methods since 2000: on the verge of a renaissance

M Yan, Y Kawamata, PS Baran - Chemical Reviews, 2017 - ACS Publications
Electrochemistry represents one of the most intimate ways of interacting with molecules. This
review discusses advances in synthetic organic electrochemistry since 2000. Enabling …

[图书][B] Organic electrochemistry

O Hammerich, B Speiser - 2016 - api.taylorfrancis.com
Organic electrochemistry is concerned with the reduction and oxidation of organic molecules
at electrodes. Although it is now more than 200 years ago that the so-called Volta pile was …

Desulfonylative electrocarboxylation with carbon dioxide

JS Zhong, ZX Yang, CL Ding, YF Huang… - The Journal of …, 2021 - ACS Publications
Electrocarboxylation of organic halides is one of the most investigated electrochemical
approaches for converting thermodynamically inert carbon dioxide (CO2) into value-added …

Deprotection of benzyl-derived groups via photochemically mesolytic cleavage of C–N and C–O bonds

K Liang, X Li, D Wei, C Jin, C Liu, C Xia - Chem, 2023 - cell.com
The benzyl group and its derivatives are the most frequently and widely utilized protective
groups in organic synthesis and are typically removed by traditional transition-metal …

Instantaneous Deprotection of Tosylamides and Esters with SmI2/Amine/Water

T Ankner, G Hilmersson - Organic Letters, 2009 - ACS Publications
Instantaneous Deprotection of Tosylamides and Esters with SmI2/Amine/Water | Organic
Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS …

Implication of a silyl cobalt dihydride complex as a useful catalyst for the hydrosilylation of imines

CC Bories, M Barbazanges, E Derat, M Petit - ACS Catalysis, 2021 - ACS Publications
Here, we describe the formation and use of silyl cobalt (III) dihydride complexes as powerful
catalysts for the hydrosilylation of a variety of imines starting from a low-valent well-defined …

Chemoselective deprotection of sulfonamides under acidic conditions: scope, sulfonyl group migration, and synthetic applications

T Javorskis, E Orentas - The Journal of Organic Chemistry, 2017 - ACS Publications
Chemoselective acidic hydrolysis of sulfonamides with trifluoromethanesulfonic acid has
been evaluated as a deprotection method and further extended to more complex synthetic …

Transition-Metal-Free and Visible-Light-Mediated Desulfonylation and Dehalogenation Reactions: Hantzsch Ester Anion as Electron and Hydrogen Atom Donor

MD Heredia, WD Guerra, SM Barolo… - The Journal of …, 2020 - ACS Publications
Novel approaches for N-and O-desulfonylation under room temperature (rt) and transition-
metal-free conditions have been developed. The first methodology involves the …