Results 181 to 190 of about 292,300 (359)

Chiral Potassium Brønsted Base‐Catalyzed Stereoselective Synthesis of 1,3‐Diols via a Tandem Allylic Isomerization/Asymmetric Aldol–Tishchenko Reaction

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
Chiral potassium base catalysts featuring 1,1´‐bi‐2‐naphthol‐derived chiral crown ethers as ligands promote a tandem allylic isomerization/asymmetric aldol‐Tishchenko reaction of allylic alcohols and aldehydes. This method provides enantioenriched 1,3‐diols with excellent diastereoselectivity and high enantioselectivity, thereby expanding the synthetic
Hiroki Ishikawa, Masahiro Sai
wiley   +1 more source

Aerobic Oxidative Dethioacetalization Catalyzed by an Iron Phthalocyanine Complex

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
A protocol for iron octacarboxyphthalocyanine‐catalyzed aerobic oxidative dethioacetalization in an aqueous solvent is developed. This method can efficiently convert a broad range of dithioacetals into the corresponding carbonyl compounds. Inspired by enzyme‐mediated redox processes, the environmentally friendly catalytic system exhibits remarkable ...
Hirofumi Ueda   +4 more
wiley   +1 more source

Synthesis of Functionalized Homoallylic Alcohols via a Salt‐Free Three‐Component Nickel‐Catalyzed Coupling Reaction

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
A nickel catalyzed three‐component coupling reaction between an aldehyde, a secondary amine, and butadiene allows a straightforward access to 5‐aminopent‐3‐en‐1‐ol scaffolds according to a salt‐free process. Key steps are oxidative coupling reaction between one aldehyde, one butadiene on a low valent nickel precursor, and the nucleophilic attack of a ...
Anthony Saint Pol   +8 more
wiley   +1 more source

Exploring the Uncharted Indolizine Chemical Space: Construction of 5‐Acylindolizines via a Domino Aldol–Vinylogous Aldol Process

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
A domino aldol condensation–intramolecular vinylogous aldol condensation process was implemented for the first time to enable access to a wide range of novel 5‐acylated indolizines with a hydrogen, an alkyl, an aryl, or an alkoxy moiety at the C7 site.
Dohui Ku, Sunhee Lee, Ikyon Kim
wiley   +1 more source

Harnessing Carbenoid Reactivity From Imidazoles and Oxiranes

open access: yesAdvanced Synthesis &Catalysis, EarlyView.
The combination of azole compounds and oxiranes exhibits carbenoid reactivity at elevated temperatures, as demonstrated by the successful benzoin condensation of aromatic aldehydes. Using this catalytic system to polymerize bifunctional aldehyde/oxirane monomers yields thermosets with glass transition temperatures above 100°C.
Matthias R. Steiner   +4 more
wiley   +1 more source

Home - About - Disclaimer - Privacy