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Radical Reaction Using an Organocopper Reagent Derived from Ethyl Bromodifluoroacetate

https://doi.org/10.1135/cccc20021285

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jlac.1995199508196openalex-snapshot

Enantioselective reformatsky reaction of methyl bromodifluoroacetate

inferredcites →https://doi.org/10.1016/0040-4020(96)00311-0openalex-snapshot

Methods for the synthesis of gem-difluoromethylene compounds

inferredcites →https://doi.org/10.1016/0040-4039(88)85053-6openalex-snapshot

Fluorine-containing organozinc reagents. IV.

inferredcites →https://doi.org/10.1016/s0022-1139(98)00193-6openalex-snapshot

Synthesis and langmuir isotherms of difluorostearic acids

inferredcites →https://doi.org/10.1016/s0040-4039(01)80239-2openalex-snapshot

2,2-Difluoro-3-hydroxyesters by reformatskii reaction

inferredcites →https://doi.org/10.1016/s0040-4039(01)81073-xopenalex-snapshot

A facile preparation of 1-perflouroalkylalkenes and alkynes. Palladium catalyzed reaction of perfluoroalkyl iodides with organotin compounds

inferredcites →https://doi.org/10.1246/cl.1992.227openalex-snapshot

Convenient Preparation of (Chlorodifluoromethyl)arenes. Useful Precursors for Aryldifluoromethyl Radicals

inferredcites →https://doi.org/10.1248/cpb.37.177openalex-snapshot

Reaction of trifluoromethyl ketones. V. Dehydration of trifluoromethylated homoallyl alcohols. Synthesis of trifluoromethylated dienes.

inferredcites →https://doi.org/10.1248/cpb.37.813openalex-snapshot

Studies on organic fluorine compounds. LIV. Synthesis of 2,2-difluoroarachidonic acid.

inferredcites →https://doi.org/10.1248/cpb.47.1013openalex-snapshot

Synthesis of Alkenyl- and Aryldifluoroacetate Using a Copper Complex from Ethyl Bromodifluoroacetate.

inferredcites →https://doi.org/10.1248/cpb.48.1023openalex-snapshot

Michael-type Reaction of Ethyl Bromodifluoroacetate with .ALPHA.,.BETA.-Unsaturated Carbonyl Compounds in the Presence of Copper Powder.

inferredcites →https://doi.org/10.1248/cpb.48.683openalex-snapshot

Synthesis of New Synthons for Organofluorine Compounds from Halothane Containing Sulfur Functional Groups

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4193557openalex-extracted

Photoredox-Catalyzed 2:2 Coupling of Aryl Ethylene and Brcf2co2me: A Facile Synthesis of Two Difluoroacetylated Hexestrol Derivatives

inferred← citeshttps://doi.org/10.1002/0471264180.or110.01openalex-snapshot

Radical Allylation, Vinylation, Allenylation, Alkynylation, and Propargylation Reactions Using Tin Reagents

inferred← citeshttps://doi.org/10.1002/9780470682531.pat0452openalex-snapshot

Fluorinated Organocopper Reagents

inferred← citeshttps://doi.org/10.1002/adsc.202100289openalex-snapshot

Visible‐Light‐Promoted Oxy‐difluoroalkylation of Aryl Alkynes for the Synthesis of β‐Fluoroenones and α‐Difluoroalkyl Ketones

inferred← citeshttps://doi.org/10.1002/chin.200313064openalex-snapshot

Radical Reaction Using an Organocopper Reagent Derived from Ethyl Bromodifluoroacetate.

inferred← citeshttps://doi.org/10.1002/cjoc.201800318openalex-snapshot

Visible Light‐Induced Methoxycarbonyldifluoromethylation of Trimethylsilyl Enol Ethers and Allyltrimethylsilanes with FSO2CF2CO2Me

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2003.11.023openalex-snapshot

Reactions of ethyl bromodifluoroacetate in the presence of copper powder

inferred← citeshttps://doi.org/10.1016/j.tet.2004.03.020openalex-snapshot

Phenyl trifluorovinyl sulfide: a radical acceptor for preparation of gem-difluoromethylene compounds

inferred← citeshttps://doi.org/10.1016/j.tet.2007.09.081openalex-snapshot

Rh-catalyzed novel α-fluoroalkylation of α,β-unsaturated ketones and its mechanism

inferred← citeshttps://doi.org/10.1016/s0022-1139(03)00003-4openalex-snapshot

1,4-Addition reaction of ethyl bromodifluoroacetate to Michael acceptors in the presence of copper powder

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01434openalex-snapshot

Copper-Catalyzed Bromodifluoroacetylation of Alkenes with Ethyl Bromodifluoroacetate

inferred← citeshttps://doi.org/10.1021/ja065484zopenalex-snapshot

Ultrafast Synthesis of Ultrahigh Molar Mass Polymers by Metal-Catalyzed Living Radical Polymerization of Acrylates, Methacrylates, and Vinyl Chloride Mediated by SET at 25 °C

inferred← citeshttps://doi.org/10.1021/jo034829iopenalex-snapshot

A Novel Method for the Preparation of α,α‘-Difluoroesters and Acids Using BrF3

inferred← citeshttps://doi.org/10.1039/c1ob05545copenalex-snapshot

Easy access to CF2-containing molecules based on the reaction of 2,2,3,3-tetrafluorooxetane with various nucleophiles

inferred← citeshttps://doi.org/10.1039/c4cc04591bopenalex-snapshot

An efficient regioselective hydrodifluoromethylation of unactivated alkenes with TMSCF 2 CO 2 Et at ambient temperature

inferred← citeshttps://doi.org/10.1039/c6cc08178aopenalex-snapshot

Oxidative trifluoromethylation and fluoroolefination of unactivated olefins

inferred← citeshttps://doi.org/10.1039/c8cc01568fopenalex-snapshot

Pd-catalyzed defluorination/arylation of α-trifluoromethyl ketones via consecutive β-F elimination and C–F bond activation

inferred← citeshttps://doi.org/10.1039/c9cc06037eopenalex-snapshot

Visible-light-triggered direct keto-difluoroacetylation of styrenes with (fluorosulfonyl)difluoroacetate and dimethyl sulfoxide leads to α-difluoroacetylated ketones

inferred← citeshttps://doi.org/10.1039/d1cc01609aopenalex-snapshot

Atom-transfer radical addition of fluoroalkyl bromides to alkenes via a photoredox/copper catalytic system

inferred← citeshttps://doi.org/10.1039/d1qo01073eopenalex-snapshot

Zinc–Brønsted acid mediated practical hydrotrifluoromethylation of alkenes with CF 3 Br

inferred← citeshttps://doi.org/10.1248/yakushi.126.1059openalex-snapshot

Synthesis of Fluorine Compounds Based on Special Property of Fluorine Compounds

inferred← citeshttps://doi.org/10.6023/cjoc202210009openalex-snapshot

Photocatalyzed 2∶2 Coupling of Styrene and BrCF2CO2Me: A Facile Synthesis of Bis-difluoroacetylated Hexestrol Derivatives

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