Articles with "diazocarbonyl compounds" as a keyword



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Asymmetric Catalytic Rearrangements with α-Diazocarbonyl Compounds.

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Published in 2022 at "Accounts of chemical research"

DOI: 10.1021/acs.accounts.1c00664

Abstract: Conspectusα-Diazocarbonyl compounds serve as nucleophiles, dipoles, carbene precursors, and rare electrophiles, enabling a vast array of organic transformations under the influence of metal catalysts. Among them, rearrangement processes are attractive and provide straightforward and efficient… read more here.

Keywords: dioxide metal; substituted diazo; group; diazocarbonyl compounds ... See more keywords
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Rh-Catalyzed Coupling of Acrylic/Benzoic Acids with α-Diazocarbonyl Compounds: An Alternative Route for α-Pyrones and Isocoumarins.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.1c03992

Abstract: A coupling of acrylic acids/benzoic acids with α-diazocarbonyl compounds has been realized by a combined catalytic system of rhodium catalyst and Zn(OAc)2 additive. The presence of Zn(OAc)2 obviously accelerates the C(sp2)-H activation and destructed the… read more here.

Keywords: benzoic acids; coupling acrylic; acids diazocarbonyl; catalyzed coupling ... See more keywords
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Trifluoromethylthiolation-Based Bifunctionalization of Diazocarbonyl Compounds by Rhodium Catalysis.

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Published in 2017 at "Organic letters"

DOI: 10.1021/acs.orglett.7b02139

Abstract: A new Rh-catalyzed, three-component reaction for the oxytrifluoromethylthiolation of α-diazoketones was developed. The SCF3 functionality was introduced using a stable dibenzenesulfonimide reagent under mild conditions. Alcohols, acetals, and ethers were used as the alkoxy sources.… read more here.

Keywords: compounds rhodium; bifunctionalization diazocarbonyl; trifluoromethylthiolation based; diazocarbonyl compounds ... See more keywords
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Displacement of Dinitrogen by Oxygen: A Methodology for the Catalytic Conversion of Diazocarbonyl Compounds to Ketocarbonyl Compounds by 2,6-Dichloropyridine-N-oxide.

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Published in 2018 at "Organic letters"

DOI: 10.1021/acs.orglett.7b03912

Abstract: Dirhodium(II) catalyzed dinitrogen extrusion from diazocarbonyl compounds by 2,6-dichloropyridine-N-oxide forms ketocarbonyl compounds in near-quantitative yields. Reactions occur at room temperature, and the pyridine product does not coordinate with dirhodium(II) to inhibit catalysis. Anhydrous tricarbonyl compounds,… read more here.

Keywords: dinitrogen; methodology; dichloropyridine oxide; diazocarbonyl compounds ... See more keywords
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Rh(III)-Catalyzed Cascade Reactions of Sulfoxonium Ylides with α-Diazocarbonyl Compounds: An Access to Highly Functionalized Naphthalenones.

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Published in 2019 at "Organic letters"

DOI: 10.1021/acs.orglett.9b00340

Abstract: An unprecedented cascade reaction of benzoyl sulfoxonium ylides with α-diazocarbonyl compounds leading to the formation of highly functionalized naphthalenones containing a β-ketosulfoxonium ylide moiety is presented. Promisingly, the naphthalenone derivative thus obtained was found to… read more here.

Keywords: iii catalyzed; sulfoxonium ylides; diazocarbonyl compounds; ylides diazocarbonyl ... See more keywords

Trifluoromethylthiolation–arylation of diazocarbonyl compounds by modified Hooz multicomponent coupling† †Electronic supplementary information (ESI) available: Experimental procedures, characterization and NMR spectra of the products. See DOI: 10.1039/c9sc00829b

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Published in 2019 at "Chemical Science"

DOI: 10.1039/c9sc00829b

Abstract: Multicomponent reaction of diazocarbonyl and dibenzenesulfonimide-SCF3 reagents with BAr4 salts in the presence of Zn(NTf2)2 gives α,α′-difunctionalized trifluoromethylthio compounds. read more here.

Keywords: trifluoromethylthiolation arylation; diazocarbonyl; arylation diazocarbonyl; modified hooz ... See more keywords