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Published in 2020 at "Tetrahedron"
DOI: 10.1016/j.tet.2020.131272
Abstract: Abstract Leveraging of 1,5-hydride shift enabled diastereoselective hydroalkylation of aryl alkenes, allowing for construction of consecutive vicinal stereogenic centers in a single process. The transformation is triggered by electrophilic alkylation of aryl alkenes with in-situ…
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Keywords:
hydride;
diastereoselective hydroalkylation;
aryl alkenes;
aryl ... See more keywords
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Published in 2021 at "Industrial & Engineering Chemistry Research"
DOI: 10.1021/acs.iecr.1c00154
Abstract: A strategy of one-pot regioselective cohydrogenation of styrene oxide (STOX) and aryl alkenes (styrene and alpha-methylstyrene) in the presence of aralkyl alcohols (1-phenylethanol and 2-phenyl-2-p...
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Keywords:
cohydrogenation styrene;
styrene oxide;
regioselective cohydrogenation;
one pot ... See more keywords
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Published in 2022 at "Inorganic chemistry"
DOI: 10.1021/acs.inorgchem.2c00036
Abstract: Selective oxidation of aryl alkenes is important for chemical synthesis reactions, in which the key lies in the rational design of efficient catalysts. Herein, four polyoxometalate (POM)-incorporated metal-organic networks, with the formulas of [Co(ttb)(H2O)3]2[SiMo12O40]·2H2O (1),…
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Keywords:
oxidation;
selective oxidation;
aryl alkenes;
incorporated metal ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02074
Abstract: A metal-free silyl-pyridylation of alkenes using silyl boronates and B2pin2 through a pyridine-mediated B-interelement activation has been demonstrated, which provides a practical strategy for a variety of C4-silylalkylated pyridines. DFT calculations and control experiments show…
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Keywords:
reaction;
reaction aryl;
alkenes silylboronate;
silylpyridylation reaction ... See more keywords
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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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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03311
Abstract: A CuH-catalyzed coupling of aryl alkenes with 3-aryl-2H-azirines has been developed to synthesize optically active β,β-disubstituted ketones. We propose that this protocol occurs through a sequence in which a chiral alkylcopper complex regioselectively attacks the…
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Keywords:
disubstituted ketones;
coupling aryl;
cuh catalyzed;
aryl alkenes ... See more keywords
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Published in 2021 at "Green Chemistry"
DOI: 10.1039/d0gc03890c
Abstract: Organoboron compounds are powerful precursors of value-added organic compounds in synthetic chemistry, and transition metal-catalysed borylation has always been dominant. To avoid toxic reagents and costs associated with metal catalysts, simpler, more economical and effective…
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Keywords:
hydroboration aryl;
selective electrocatalytic;
electrocatalytic hydroboration;
chemistry ... See more keywords
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Published in 2022 at "Frontiers in Chemistry"
DOI: 10.3389/fchem.2022.851674
Abstract: C-N bond formation is one of the most commonly used reactions in medicinal chemistry. Herein, we report an efficient Pd-promoted hydroamination reaction between DNA-conjugated aryl alkenes and a wide scope of aliphatic amines. The described…
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Keywords:
dna;
dna conjugated;
chemistry;
hydroamination ... See more keywords