about
Dual gold and photoredox catalysed C-H activation of arenes for aryl-aryl cross couplingsA Novel Heterostructure of BiOI Nanosheets Anchored onto MWCNTs with Excellent Visible-Light Photocatalytic Activity.Functionalization of C-H Bonds by Photoredox Catalysis.Circumventing Intrinsic Metal Reactivity: Radical Generation with Redox-Active Ligands.Visible-Light-Promoted Synthesis of 1,4-Dicarbonyl Compounds via Conjugate Addition of Aroyl Chlorides.Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones.Robust Cooperative Photo-oxidation of Sulfides without Sacrificial Reagent under Air Using a Dinuclear RuII -CuII Assembly.Dual gold/photoredox-catalyzed bis-arylative cyclization of chiral homopropargyl sulfonamides with diazonium salts: rapid access to enantioenriched 2,3-dihydropyrroles.Teaching Old Compounds New Tricks: DDQ-Photocatalyzed C-H Amination of Arenes with Carbamates, Urea, and N-Heterocycles.Visible-Light-Induced Direct Oxidative C-H Amidation of Heteroarenes with Sulfonamides.Sulfonylative and Azidosulfonylative Cyclizations by Visible-Light-Photosensitization of Sulfonyl Azides in THF.Visible-light-induced tandem cyclization of 2-alkynylanilines with disulfides: a convenient method for accessing benzothiophenes under transition-metal-free and photocatalyst-free conditions.Merging visible-light photoredox and copper catalysis in catalytic aerobic oxidation of amines to nitriles.Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.Dual gold photoredox C(sp(2))-C(sp(2)) cross couplings - development and mechanistic studies.Visible light-induced transition metal-catalyzed transformations: beyond conventional photosensitizers.A visible-light-activated rhodium complex in enantioselective conjugate addition of α-amino radicals with Michael acceptors.Organic sponge photocatalysisVisible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions
P2860
Q33669902-07EABFC0-C16E-4DF2-84CF-430C444CEE8FQ37628610-02BA1B5E-420F-4FC2-B5E6-D8F50BF83A17Q39079192-9B3A6F90-28FC-4C7E-AA34-4BECD99E70B5Q46311982-EF3ADB3B-7EF7-49D0-B590-3563BD666C20Q47188855-762051BF-FAE8-4406-B1A3-3EC80AF21EEEQ47375255-AF3EE6B4-7213-4FA2-9746-81591217BC9DQ47878334-A076AA63-DD4F-4A26-8B71-C2C2FECFA49EQ48027154-95C2990F-8F6E-4755-8DEB-C2F8006E5222Q48292790-8D2E6A74-216F-4A87-A7DA-7BEAFF4B75F9Q48293278-FAF27CB1-34F4-4F4E-8D48-89FF408EAE61Q48295982-DAE10A5F-8125-4579-B3AC-471966E549A3Q48670258-AAB4ABE0-27A3-4202-84D4-380D3FF17F8DQ51088002-3F18291D-B1DB-4127-8A44-0514E8A86740Q51229317-A83C1E9E-7F95-4773-8BF7-A1D46F213602Q51229809-F8346FA9-C02A-4010-AEAB-9F963192EB0EQ52545564-2FD2113F-82E7-4951-A647-47619EB12E0DQ52596868-9FBC82E5-890E-48CD-94CA-97C0551C190BQ57960828-DDD96C4A-3CF0-46FE-B274-7A0028F6D3E9Q58623754-995E2280-0A11-4A0F-9C4C-21A8F4AC0471
P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Cooperative photoredox catalysis.
@en
Cooperative photoredox catalysis.
@nl
type
label
Cooperative photoredox catalysis.
@en
Cooperative photoredox catalysis.
@nl
prefLabel
Cooperative photoredox catalysis.
@en
Cooperative photoredox catalysis.
@nl
P2860
P356
P1476
Cooperative photoredox catalysis
@en
P2093
Jincai Zhao
Xiaodong Chen
P2860
P304
P356
10.1039/C5CS00659G
P50
P577
2016-05-01T00:00:00Z