Enantioselective radical reactions using chiral catalysts
Benefiting from the impressive increase in fundamental knowledge, the last 20 years have
shown a continuous burst of new ideas and consequently a plethora of new catalytic …
shown a continuous burst of new ideas and consequently a plethora of new catalytic …
Titanium catalysis for the synthesis of fine chemicals–development and trends
M Manßen, LL Schafer - Chemical Society Reviews, 2020 - pubs.rsc.org
Titanium is the second most abundant transition metal and is already a key player in
important industrial processes (eg polyethylene). Titanium is an attractive metal to use for …
important industrial processes (eg polyethylene). Titanium is an attractive metal to use for …
Multiplicative enhancement of stereoenrichment by a single catalyst for deracemization of alcohols
L Wen, J Ding, L Duan, S Wang, Q An, H Wang, Z Zuo - Science, 2023 - science.org
Stereochemical enrichment of a racemic mixture by deracemization must overcome
unfavorable entropic effects as well as the principle of microscopic reversibility; recently …
unfavorable entropic effects as well as the principle of microscopic reversibility; recently …
Synthesis of azabicyclo [3.1. 1] heptenes enabled by catalyst-controlled annulations of bicyclo [1.1. 0] butanes with vinyl azides
Z Lin, H Ren, X Lin, X Yu, J Zheng - Journal of the American …, 2024 - ACS Publications
Bridged bicyclic scaffolds are emerging bioisosteres of planar aromatic rings under the
concept of “escape from flatland”. However, adopting this concept into the exploration of …
concept of “escape from flatland”. However, adopting this concept into the exploration of …
Recent advances in the chemistry of ketyl radicals
Ketyl radicals are valuable reactive intermediates for synthesis and are used extensively to
construct complex, functionalized products from carbonyl substrates. Single electron transfer …
construct complex, functionalized products from carbonyl substrates. Single electron transfer …
Additive effects on asymmetric catalysis
L Hong, W Sun, D Yang, G Li, R Wang - Chemical Reviews, 2016 - ACS Publications
This review highlights a number of additives that can be used to make asymmetric reactions
perfect. Without changing other reaction conditions, simply adding additives can lead to …
perfect. Without changing other reaction conditions, simply adding additives can lead to …
Modern applications of low-valent early transition metals in synthesis and catalysis
Low-valent early transition metals are often intrinsically highly reactive as a result of their
strong propensity toward oxidation to more stable high-valent states. Harnessing these …
strong propensity toward oxidation to more stable high-valent states. Harnessing these …
Enantioselective photoredox catalysis enabled by proton-coupled electron transfer: development of an asymmetric aza-pinacol cyclization
LJ Rono, HG Yayla, DY Wang… - Journal of the …, 2013 - ACS Publications
The first highly enantioselective catalytic protocol for the reductive coupling of ketones and
hydrazones is reported. These reactions proceed through neutral ketyl radical intermediates …
hydrazones is reported. These reactions proceed through neutral ketyl radical intermediates …
Reductive deoxygenative functionalization of alcohols by first‐row transition metal catalysis
X Pang, XZ Shu - Chinese Journal of Chemistry, 2023 - Wiley Online Library
Comprehensive Summary Alcohols are among the most accessible functionalities. Catalytic
deoxygenative functionalization of alcohols is highly synthetically appealing. While …
deoxygenative functionalization of alcohols is highly synthetically appealing. While …
Divergent Iron‐Catalyzed Coupling of O‐Acyloximes with Silyl Enol Ethers
HB Yang, N Selander - Chemistry–A European Journal, 2017 - Wiley Online Library
An iron‐catalyzed coupling reaction of O‐acyloximes and O‐benzoyl amidoximes with silyl
enol ethers is reported. The protocol provides access to functionalized pyrroles, 1, 6 …
enol ethers is reported. The protocol provides access to functionalized pyrroles, 1, 6 …