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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…
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Keywords:
hydroacylation;
aroyl fluorides;
hydroacylation aryl;
catalyzed hydroacylation ... See more keywords
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1
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…
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Keywords:
hydroacylation;
catalysis chelation;
dual catalysis;
terminal alkynes ... See more keywords
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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…
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Keywords:
oxides effective;
effective controlling;
azine;
controlling groups ... See more keywords
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1
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…
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Keywords:
hydroacylation conjugate;
conjugate addition;
saturated heterocycles;
heterocycles hydroacylation ... See more keywords
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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.…
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Keywords:
lewis acid;
system;
ketone hydroacylation;
assisted dirhodium ... See more keywords
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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…
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Keywords:
mechanism;
aucn catalyzed;
cyanide ion;
ion ... See more keywords