A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
about
C-H bond halogenation catalyzed or mediated by copper: an overviewA convenient photocatalytic fluorination of unactivated C-H bonds.Decarboxylative Fluorination of Aliphatic Carboxylic Acids via Photoredox Catalysis.A Visible-Light-Mediated Radical Smiles Rearrangement and its Application to the Synthesis of a Difluoro-Substituted Spirocyclic ORL-1 AntagonistCatalytic enantioselective cyclization and C3-fluorination of polyenes.Copper-catalyzed, directing group-assisted fluorination of arene and heteroarene C-H bonds.Oxidative aliphatic C-H fluorination with manganese catalysts and fluoride ionRecent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.C-H functionalisation of cycloalkanes.Vanadium-Catalyzed C(sp(3))-H Fluorination Reactions.The Uranyl Cation as a Visible-Light Photocatalyst for C(sp(3) )-H Fluorination.Ligand-Enabled Stereoselective β-C(sp(3))-H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids.Scalable, Electrochemical Oxidation of Unactivated C-H Bonds.Charge-transfer-directed radical substitution enables para-selective C-H functionalization.Visible light-promoted metal-free C-H activation: diarylketone-catalyzed selective benzylic mono- and difluorination.Visible light-promoted metal-free sp(3)-C-H fluorination.Copper-catalyzed regioselective fluorination of allylic halides.Ketones as directing groups in photocatalytic sp3 C-H fluorination.C(sp3)-F bond formation: a free-radical approach.Selective Radical Fluorination of Tertiary Alkyl Halides at Room Temperature.Hydrogenation of fluoroarenes: Direct access to all-cis-(multi)fluorinated cycloalkanes.Unstrained C-C bond activation and directed fluorination through photocatalytically-generated radical cations.Transition-metal-free visible-light photoredox catalysis at room-temperature for decarboxylative fluorination of aliphatic carboxylic acids by organic dyes.Selective fluorination of alkyl C-H bonds via photocatalysis.Development of a Rhodium(II)-Catalyzed Chemoselective C(sp(3) )-H Oxygenation.A General Strategy for Aliphatic C-H Functionalization Enabled by Organic Photoredox Catalysis.Site-selective 18F fluorination of unactivated C-H bonds mediated by a manganese porphyrin.Manganese-catalyzed oxidative benzylic C-H fluorination by fluoride ions.Revised role of selectfluor in homogeneous Au-catalyzed oxidative C-O bond formations.Silver-catalyzed oxidative activation of benzylic C-H bonds for the synthesis of difluoromethylated arenes.Ketone-catalyzed photochemical C(sp3)-H chlorination.A Convenient Late-Stage Fluorination of Pyridylic C-H Bonds with N-Fluorobenzenesulfonimide.Selective electrochemical generation of benzylic radicals enabled by ferrocene-based electron-transfer mediators.
P2860
Q26776189-1A0162A0-E22B-46BA-B89F-945EE230B7D8Q34412063-9345B9C6-8589-4D95-AD9E-41A27662BF96Q34472165-5D374E3C-B28A-48D1-B9BF-43677B024E4BQ36497550-EBC713A3-49F8-48FC-A938-BA1EC0DA2BA8Q36554570-45488E02-3770-4917-8F2B-6262B812CE4DQ37069922-1F06E7EF-01AE-4846-A412-983F7874C9A3Q37678426-2A34F22C-58DF-4A4E-9DD7-F64B1D8213AFQ38675808-27994597-E28C-45D2-AD7C-95B3219A9574Q39031084-EA287F37-760F-455B-8F1E-D19AFEC80FBBQ41013531-F77A13F1-B73E-4275-8851-8F60D9B16408Q41649198-67581FE6-FFDD-42C7-8099-FAB078EC4861Q42015434-007AE148-AA47-4D5F-A508-A10C5094FDAEQ42211441-1850B71C-890C-4F9B-81EA-C38FCC0FFB0FQ42407950-DF789F3B-3ECA-48D0-8000-8A597F2E6F6EQ42773523-7FB12FCB-BA58-42B3-8AB1-7A55D61586E8Q42872338-38FE1FB4-5CA3-4963-93EC-AD6C567E9DA5Q44295386-EE7A7F00-9FDA-4102-84E1-8DEA6060F27DQ45929022-AAAB31B4-27EF-408D-8F93-0E63652D7D0EQ46526436-EFE3D39D-DF63-424E-A09C-FD9DB0865292Q48199293-1CEA3A8C-DA71-4366-BEB5-D326EF1F7E89Q48257084-8F881DB7-2C3D-461D-80B8-FF6D84B42AE4Q49707412-F92A0688-8A1A-4118-8DE8-6215040BFDEFQ50264751-7AB2BE8B-CB20-439B-894A-78229DADD284Q51079249-7AE4F797-7D12-4346-BB1D-6604713BAD99Q51794114-039586FE-9F85-4C43-BDA9-AAB63EC15644Q52361631-36A25191-7DE1-476B-808E-484BCC59CFC8Q52575985-68DDCD6C-050B-4D02-AA20-AA49441401C5Q53111711-A59F165A-E066-4B5A-8D4E-45D59D294C65Q53421753-C2E6019F-3FC3-4B87-BFAF-45E4F523F5E6Q53567080-6B41AD77-3471-4440-8EF4-BB73D7625839Q53758964-54C6A26F-C17A-45B2-BD15-39ECE7849C7CQ54611862-BC9E4B22-A2AB-42B5-A265-9DBD06AE22D0Q55395131-64523D6D-A5D8-48A0-83EE-91705E829437
P2860
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
description
2012 nî lūn-bûn
@nan
2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
name
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@ast
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@en
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@nl
type
label
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@ast
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@en
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@nl
prefLabel
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@ast
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@en
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@nl
P2093
P2860
P356
P1476
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination.
@en
P2093
Cody Ross Pitts
David Curtin Miller
Ellen Urheim
Maxwell Gargiulo Holl
Nathan Haselton
Steven Bloom
Thomas Lectka
P2860
P304
10580-10583
P356
10.1002/ANIE.201203642
P407
P577
2012-09-13T00:00:00Z