Articles with "hydroacylation" as a keyword



Exogenous Ligand-Free NiH-Catalyzed Hydroacylation of Aryl Alkenes with Aroyl Fluorides.

Sign Up to like & get
recommendations!
Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c02110

Abstract: Acyl fluorides have emerged as efficient acyl group donors, but these attractive reagents have rarely been utilized in transition-metal-catalyzed hydroacylation. Herein we report a nickel hydride-catalyzed hydroacylation of aryl alkenes using aroyl fluorides. The reaction… read more here.

Keywords: hydroacylation; aroyl fluorides; hydroacylation aryl; catalyzed hydroacylation ... See more keywords
Photo by shelbymdesign from unsplash

Photoredox-Ni Dual Catalysis: Chelation-Free Hydroacylation of Terminal Alkynes.

Sign Up to like & get
recommendations!
Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c03481

Abstract: Hydroacylation of alkynes is undoubtedly the simplest and most atom-efficient approach for the synthesis of enones with diverse synthetic applications. Despite significant progress in hydroacylations, no hydroacylations exist that make use of aldehydes without a… read more here.

Keywords: hydroacylation; catalysis chelation; dual catalysis; terminal alkynes ... See more keywords
Photo by vlisidis from unsplash

Azine-N-oxides as effective controlling groups for Rh-catalysed intermolecular alkyne hydroacylation

Sign Up to like & get
recommendations!
Published in 2021 at "Chemical Science"

DOI: 10.1039/d1sc03915f

Abstract: Heterocycle-derived aldehydes are challenging substrates in metal-catalysed hydroacylation chemistry. We show that by using azine N-oxide substituted aldehydes, good reactivity can be achieved, and that they are highly effective substrates for the intermolecular hydroacylation of… read more here.

Keywords: oxides effective; effective controlling; azine; controlling groups ... See more keywords
Photo from wikipedia

Diverse saturated heterocycles from a hydroacylation/conjugate addition cascade

Sign Up to like & get
recommendations!
Published in 2022 at "Chemical Science"

DOI: 10.1039/d1sc06900d

Abstract: Rhodium-catalyzed hydroacylation using alkynes substituted with pendant nucleophiles, delivers linear α,β-unsaturated enone intermediates with excellent regioselectivity. These adducts are used to construct a broad range of diversely substituted, saturated O-, N- and S-heterocycles in a… read more here.

Keywords: hydroacylation conjugate; conjugate addition; saturated heterocycles; heterocycles hydroacylation ... See more keywords
Photo by vlisidis from unsplash

Lewis Acid-assisted Dirhodium(II)-catalyzed Ketone Hydroacylation

Sign Up to like & get
recommendations!
Published in 2017 at "Chemistry Letters"

DOI: 10.1246/cl.160862

Abstract: The combination of a Rh(II) salt and a Lewis acid, Sc(OTf)3, as a highly active and robust cooperative catalyst system for ketone hydroacylation was developed. The catalyst system showed high turnover numbers (up to ca.… read more here.

Keywords: lewis acid; system; ketone hydroacylation; assisted dirhodium ... See more keywords
Photo by roanlavery from unsplash

Mechanistic Insight Into the AuCN Catalyzed Annulation Reaction of Salicylaldehyde and Aryl Acetylene: Cyanide Ion Promoted Umpolung Hydroacylation/Intramolecular Oxa-Michael Addition Mechanism

Sign Up to like & get
recommendations!
Published in 2019 at "Frontiers in Chemistry"

DOI: 10.3389/fchem.2019.00557

Abstract: The detailed mechanism of the AuCN-catalyzed annulation of salicylaldehyde (SA) and phenyl acetylene leading to isoflavanone-type complexes has been investigated via density functional theory (DFT) calculations. Reaction pathways and possible stationary points are obtained with… read more here.

Keywords: mechanism; aucn catalyzed; cyanide ion; ion ... See more keywords