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Recent advances in acyl radical enabled reactions between aldehydes and alkenes

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TLDR
A summary of the state of the art in this field with a specific emphasis on the working models and corresponding mechanisms is provided in this paper, where the discussion is divided according to the kind of alkenes and reaction type.
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This article is published in Chemical Communications.The article was published on 2021-06-22. It has received 23 citations till now.

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Cu(I)-Catalyzed Chemo- and Enantioselective Desymmetrizing C-O Bond Coupling of Acyl Radicals.

TL;DR: In this paper , a transition-metal-catalyzed enanti-lective desymmetrizing C-O bond coupling of acyl radicals was proposed for the rapid preparation of chiral C3 building blocks from readily available alcohols, particularly the industrially relevant glycerol.
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Tandem vinyl radical Minisci-type annulation on pyridines: one-pot expeditious access to azaindenones

TL;DR: In this paper, a new regiospecific alkylative/alkenylative cascade annulation of pyridines has been achieved whilst the corresponding classic Minisci alky lative annulation failed.
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α-Acylation of Alkenes by a Single Photocatalyst.

TL;DR: In this paper , a single photocatalyst driven α-acylation of fluoromethyl-, alkyl-, sulfonyl- and thiolation of alkenes with high chemo-and regioselectivity under extremely mild conditions is presented.
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Visible-light induced transition-metal and photosensitizer-free conversion of aldehydes to acyl fluorides under mild conditions

TL;DR: In this article , a green method for the synthesis of acyl fluorides from aldehydes via C(sp2)-H fluorination is presented, in the absence of transition-metal and external photosensitizer.
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Photoredox‐Mediated Deoxygenative Radical Additions of Aromatic Acids to Vinyl Boronic Esters and gem‐Diborylalkenes

TL;DR: In this paper , a deoxygenative radical addition of aromatic carboxylic acids to gem-dibortlalkenes is described, in which the reaction proceeds under mild photoredox catalysis and involves the photochemical C−O bond activation of aromatic CARB in the presence of PPh3.
References
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Journal ArticleDOI

Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond functional group transformations.

TL;DR: This work over the past several years to form carbon-carbon bonds directly from two different C-H bonds under oxidative conditions, cross-dehydrogenative coupling (CDC) is described, which provides an alternative to the separate steps of prefunctionalization and defunctionsalization that have traditionally been part of synthetic design.
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Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation

TL;DR: This critical review covers the recent progresses on the regioselective dehydrogenative direct coupling reaction of heteroarenes, including arylation, olefination, alkynylation, and amination/amidation mainly utilizing transition metal catalysts.
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Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions

TL;DR: Oxidative X-X Bond Formations between Two Nucleophiles 1819 5.1.
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