About: Decarboxylative sp C-N coupling via dual copper and photoredox catalysis

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scientific article published in Nature

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) scientific article published in Nature (en) im Juli 2018 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована в Nature в липні 2018 (uk)
publication date	wds:Q59060139-E60C0A10-A85C-4BC9-A02D-9EF566139302
publication date	2018-07-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59060139-6A596279-7567-49BF-8D60-27C401BE993E
language of work or name	English
exact match	wds:Q59060139-D439A829-205E-4318-A832-4783F8084C50
exact match	https://scigraph.springernature.com/pub.10.1038/s41586-018-0234-8
cites work	wds:Q59060139-10A684F7-BBEB-41F8-BBFE-B4BC0BE1E1D0 wds:Q59060139-3CAA788E-EAB7-4512-93C1-AFCD985E46F1 wds:Q59060139-476B42E9-6894-4A10-A73C-1232E4DF8582 wds:Q59060139-49A12D0B-F09A-4D19-B5E8-99A1C66B9B60 wds:Q59060139-49FE1912-16BA-4C68-BC57-0BA562E74F20 wds:Q59060139-4FD50E9F-E81E-44F4-A41F-0FCC55E7C43D wds:Q59060139-51DAE9A0-7505-40B8-9ABB-7F7BA76DEC64 wds:Q59060139-634DCAD8-9BC9-4917-9173-6654972852A3 wds:Q59060139-637F3A03-1B5B-40B3-B6AA-4DA810331DB6 wds:Q59060139-68FFA457-63D2-4E49-9D4C-131148A10989 wds:Q59060139-70CF3523-0390-4F3C-9520-3F5B45FFD2FC wds:Q59060139-7A9DD431-3A6D-4F38-BA3E-C7F5B2DE34A5 wds:Q59060139-7B5799BA-9401-4E9B-B5B1-767CB698D552 wds:Q59060139-91FF3A1D-1B08-44FF-870A-7C6553E6C4D0 wds:Q59060139-944B2A96-82E5-4BAB-BE74-D7A19DE312D4 wds:Q59060139-9891AFCC-1B88-4010-8344-5FA1ABCE7689 wds:Q59060139-999F45BF-B6B0-43ED-BFD4-16626D0C3DA7 wds:Q59060139-9DF5D4F9-8DE1-440C-AD13-9D719D1EC053 wds:Q59060139-9E1E8944-A4A2-4885-AD00-4DCF887B2E53 wds:Q59060139-C06F6683-8582-45BB-AD2F-AC65DF656467 wds:Q59060139-CC9D8018-1129-4EE8-B92A-61F68AE6D59D wds:Q59060139-D53204F6-AC1F-4A3C-A5CC-8C5A6D906E7B wds:Q59060139-D7D5D3E4-CAB2-4499-8E24-25779F510491 wds:Q59060139-EA3C98C4-D653-40CB-A591-59DF0C78BE4C
cites work	Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development Analysis of the structural diversity, substitution patterns, and frequency of nitrogen heterocycles among U.S. FDA approved pharmaceuticals Chemoselectivity and the curious reactivity preferences of functional groups Mitsunobu and related reactions: advances and applications Dual catalysis. Merging photoredox with nickel catalysis: coupling of α-carboxyl sp³-carbons with aryl halides Equilibrium acidities in dimethyl sulfoxide solution Photoredox Catalysis in Organic Chemistry Late Transition Metal-Catalyzed Hydroamination and Hydroamidation Application of the bicyclo[1.1.1]pentane motif as a nonclassical phenyl ring bioisostere in the design of a potent and orally active γ-secretase inhibitor A Review on the Use of Sodium Triacetoxyborohydride in the Reductive Amination of Ketones and Aldehydes Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes 20. Hydrazide und Azide organischer Säuren I. Abhandlung Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions A General Small-Scale Reactor To Enable Standardization and Acceleration of Photocatalytic Reactions Palladium-Catalyzed Cross Coupling of Secondary and Tertiary Alkyl Bromides with a Nitrogen Nucleophile Photoinduced, Copper-Catalyzed Decarboxylative C-N Coupling to Generate Protected Amines: An Alternative to the Curtius Rearrangement Copper-Catalyzed Alkylation of Aliphatic Amines Induced by Visible Light. Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis Recent advances in polyaniline research: Polymerization mechanisms, structural aspects, properties and applications On the Basicity of Conjugated Nitrogen Heterocycles in Different Media Alcohols as Latent Coupling Fragments for Metallaphotoredox Catalysis: sp3-sp2 Cross-Coupling of Oxalates with Aryl Halides. Synthesis of highly functionalized polycyclic quinoxaline derivatives using visible-light photoredox catalysis Selected Copper-Based Reactions for C-N, C-O, C-S and C-C Bond Formation. A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate
author name string	wds:Q59060139-773AD53F-8DE5-4A9A-9A32-E156BE5E6064
author name string	Xiaheng Zhang
rdfs:label	Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (en) Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (nl)
skos:prefLabel	Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (en) Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (nl)
name	Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (en) Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (nl)
author	wds:Q59060139-A139DB75-05DB-4985-88C3-472E025FD6E4 wds:Q59060139-F89993DB-3747-4AEB-9C6E-7A427B95FD33
author	David MacMillan Yufan Liang
title	wds:Q59060139-B901E253-1A4F-4902-9372-EEF03309B7C4
title	Decarboxylative sp C-N coupling via dual copper and photoredox catalysis (en)
page(s)	wds:Q59060139-62DDAF04-E245-4AE6-AE9E-EFB967CFA06C
page(s)	83-88
instance of	wds:Q59060139-557D47B2-1878-46BF-9AFC-DF5EA818E931
instance of	scholarly article
PubMed ID	wds:Q59060139-DEB947B9-29E1-4878-804B-E34796E7D5C1
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/29925943
PubMed ID	29925943
published in	wds:Q59060139-420C6D32-BC73-459F-B2F1-DD984F77E2A6
published in	Nature
issue	wds:Q59060139-53E31B5B-61D0-4AD8-B242-548AE2257009
volume	wds:Q59060139-58EBAE24-0EBD-4A0A-B53F-5601D27737E7
issue	7712
volume	559
DOI	wds:Q59060139-FC71E583-8E1F-4F78-8FE0-CCAC0CAD540E
DOI	http://dx.doi.org/10.1038/S41586-018-0234-8
DOI	10.1038/S41586-018-0234-8
Dimensions Publication ID	wds:Q59060139-0FB35808-6B1A-4721-AE61-D9F15296D9C6
Dimensions Publication ID	1104915638
PMCID	wds:Q59060139-608B0080-8150-4B2A-A361-2D068A05555B
PMCID	6106865
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59060139
is cites work of	The merger of decatungstate and copper catalysis to enable aliphatic C(sp3)-H trifluoromethylation A transition-metal-free & diazo-free styrene cyclopropanation Photocatalytic Oxyamination of Alkenes: Copper(II) Salts as Terminal Oxidants in Photoredox Catalysis Nickel-Catalyzed Decarbonylative Amination of Carboxylic Acid Esters

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