Enantioselective α-benzylation of aldehydes via photoredox organocatalysis - Test2 - elhamkhani - TriplyDB

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

http://www.wikidata.org/entity/Q24600920

about

Visible light photocatalysis of radical anion hetero-Diels–Alder cycloadditions Photocatalytic reductive cyclizations of enones: Divergent reactivity of photogenerated radical and radical anion intermediates Solar synthesis: prospects in visible light photocatalysis Photoredox Catalysis in Organic Chemistry Visible-light organic photocatalysis for latent radical-initiated polymerization via 2e⁻/1H⁺ transfers: initiation with parallels to photosynthesis.Intermolecular atom transfer radical addition to olefins mediated by oxidative quenching of photoredox catalysts.Oxidative photoredox catalysis: mild and selective deprotection of PMB ethers mediated by visible light.Photoredox catalyzed C-P bond forming reactions-visible light mediated oxidative phosphonylations of amines.Visible-light photoredox catalyzed oxidative Strecker reaction.Visible light-induced oxidative coupling reaction: easy access to Mannich-type products.Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions.Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis.Metal and metal-free photocatalysts: mechanistic approach and application as photoinitiators of photopolymerization Friedel-Crafts amidoalkylation via thermolysis and oxidative photocatalysis.Palladium-catalyzed, pyrrolidine-mediated arylmethylation of ketones and aldehydes with coumarinyl(methyl) acetates Synthesis of 2,5-Diaryl-1,5-dienes from Allylic Bromides Using Visible-Light Photoredox Catalysis A Visible-Light-Mediated Radical Smiles Rearrangement and its Application to the Synthesis of a Difluoro-Substituted Spirocyclic ORL-1 Antagonist Carbene-catalysed reductive coupling of nitrobenzyl bromides and activated ketones or imines via single-electron-transfer process.Redox mediators in visible light photocatalysis: photocatalytic radical thiol-ene additions.Photofunctional triplet excited states of cyclometalated Ir(III) complexes: beyond electroluminescence.Synthetic applications of photoredox catalysis with visible light.Photochemical transformations accelerated in continuous-flow reactors: basic concepts and applications.Photochemistry and radical chemistry under low intensity visible light sources: application to photopolymerization reactions.Enantioselective catalysis of photochemical reactions.Catalysis of Radical Reactions: A Radical Chemistry Perspective.Ligand functionalization as a deactivation pathway in a fac-Ir(ppy)3-mediated radical addition Dual Catalysis Strategies in Photochemical Synthesis.Visible-light photoredox catalysis enabled bromination of phenols and alkenes.Photocatalysis in organic and polymer synthesis.Decarboxylative arylation of α-amino acids via photoredox catalysis: a one-step conversion of biomass to drug pharmacophore.Photoredox-Mediated Routes to Radicals: The Value of Catalytic Radical Generation in Synthetic Methods Development.Photoinduced Cleavage of N-N Bonds of Aromatic Hydrazines and Hydrazides by Visible Light.Visible light-mediated oxidative quenching reaction to electron-rich epoxides: highly regioselective synthesis of α-bromo (di)ketones and mechanism study.Photo-organocatalytic Enantioselective Perfluoroalkylation of β-Ketoesters.An approach for the synthesis of nakamuric acid.Total synthesis of (+)-gliocladin C enabled by visible-light photoredox catalysis.Visible-light photoredox catalysis in flow.Tunable chiral metal organic frameworks toward visible light-driven asymmetric catalysis.Single-electron transmetalation: an enabling technology for secondary alkylboron cross-coupling.Transition metal photoredox catalysis of radical thiol-ene reactions.

P2860

Q24620526-8FED3C7E-AF76-4700-8E6F-4806DA568264 Q24634554-E3A9F31F-2E8E-4DEA-9754-0B323CF5ED0E Q27010410-3E46D076-B947-4B0E-87F0-4F939A3BC9E3 Q28829372-74EF65C9-A84C-4028-887E-7B0EA993F543 Q33715934-F2FA86CB-D6D2-4F3E-8EAF-DCA9A59104C4 Q33838783-F642A310-59A1-4C8D-8F18-96C897AD1B63 Q33853774-A500C06B-4E22-4CFA-91EC-1C6E2EAFBFEC Q34196786-E6658887-F469-410E-9475-833D9F2DC1BC Q34229152-48BCF6D7-38F4-4A4D-87F9-8BA2EC021248 Q34247767-E656071C-AC0D-4887-8680-03A2D34AA527 Q34301296-CB890DB2-59E0-48F6-B8E8-43F7F630F3D1 Q34333964-396A4501-E4E6-4F9D-A6E3-8A6E066FDDD9 Q35159188-9E52AE8E-77A0-402F-846A-B6E5A0DD1476 Q35990129-E45DE38F-8E9D-4BE4-9FCD-626B0D2BA169 Q36238706-26A85974-C94A-40FD-AB0F-3ECF9A3D4248 Q36420582-2C32D49B-FB8D-41B3-8A79-167E357C00D6 Q36497550-F90C39F3-D15F-43D8-A889-18AAFF81079C Q37315016-F1917228-CCB9-449D-9BE0-4622F34380D4 Q37701566-82492677-3208-4D66-A021-311DF9796050 Q38026452-6DD687CB-9D86-4069-990A-5711035AFFB3 Q38083214-790A0730-A9B6-489E-A6EF-D3E57F889841 Q38233279-C9763272-373C-444E-A080-2B2202C5C86F Q38252590-576EBD85-1404-4880-A4B8-09E9EBD304F9 Q38366538-99A6EAEF-1A70-46B3-8E7B-3835FA6DACC1 Q38605492-8101142D-724E-4F23-9807-81A5464E1BD5 Q38679889-ECB4D993-EDB2-4929-9239-F7486C42B371 Q38816266-995E1322-EE52-4BB8-9513-FA06376880BB Q38968715-523EE1E4-DE16-4618-ABAC-22A6496DA350 Q39000568-DA4E15B4-615F-4820-AA1B-DAECEDD999C8 Q39045035-075C9D10-1277-4F0F-8E6F-05693C5DC3E2 Q39245541-7B06A129-4C39-4D59-8131-404D31DC2B4E Q39330137-4D945542-5021-476A-B9B5-69E80C659489 Q40128074-2791E03F-A4D9-423F-972A-809B7142D9D7 Q40555683-83A21DB1-7D8B-498C-884A-293F303B0845 Q40622829-77129035-A7A4-4D2E-BD36-B1CFA0C2E078 Q41207267-3665A6B1-C5A7-4D24-ADB3-C905796F077D Q41207343-87186C2E-4FB9-4BDC-A505-CE77452AE062 Q41456802-CC1901DA-B748-42A7-A0C0-A981202FEF3A Q41761401-1340DB38-753E-46E1-B057-2BF44CE4DA96 Q41771271-0EC7FC7C-8C72-4AF4-9AD2-F43CD121B2B2

P2860

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

http://www.wikidata.org/entity/Q24600920

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@ast

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@en

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@nl

type

label

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@ast

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@en

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@nl

prefLabel

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@ast

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@en

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@nl

P1433

Q24600920-7F1A824A-AB8A-454D-8C7E-8B52251A0E1A

P1476

Q24600920-239A9B7E-A45D-4505-ADD5-E02C820B5976

P2093

Q24600920-0401C7E7-634E-440A-A8AE-CBB0DE456FD3

Q24600920-866F9E1E-E05C-4B2C-8E57-315A939F8B6F

Q24600920-B44BACA1-682A-4FC9-ABD3-0F470888CFE6

Q24600920-BCD9F18E-836F-46F8-B60E-B5A398886258

P2860

Q24600920-0334BB35-0B50-4085-96F9-D7C5A34A4541

Q24600920-05F5969B-1C1B-4CAB-9369-DB3C80CABDE7

Q24600920-07ADA121-5214-434C-9445-6169E70688E5

Q24600920-13060D0C-19F1-44B5-9720-FDA2C704BB8F

Q24600920-157A7987-913C-431D-94E0-2AE1246D64C2

Q24600920-340DDADD-C9AE-48F6-BE7E-7CA1721761A4

Q24600920-3EB66BC8-B1B0-4166-9616-9D69413846B4

Q24600920-4476D00C-7163-42AE-853D-ABEFFE837ECE

Q24600920-44DD9683-4BB3-448A-B79C-A968FFECB5D9

Q24600920-53D400E8-C553-4611-BEEC-074BB09CE391

P304

Q24600920-2CA147F5-8E1B-4B8D-8B4A-6FA0C36779DB

P31

Q24600920-1DF8E465-3529-4A03-970E-5BDDEBF3415A

P3181

Q24600920-AD80D1BB-4A75-462F-9844-EC16550151DE

P356

Q24600920-CD9FA4D6-0E1B-4BF3-992E-086233606C9D

P407

Q24600920-70621E7A-D770-49FD-9DEC-8FA7ED85E4DE

P433

Q24600920-95E5B75B-7A7B-4667-92F7-031EE2B13F67

P478

Q24600920-96DEE444-C362-41F2-83F8-B09B5CEB239F

P577

Q24600920-F92FE049-C46C-4B88-BD13-1DF4BE863D93

P5875

Q24600920-0321AD1E-4893-41A6-B069-DB61EDAF6BD4

P698

Q24600920-677794AC-352C-41B4-86E7-13A6359A0A86

P921

Q24600920-651803A3-226C-4E9B-BC7E-47A9B19B2DBB

Q24600920-7315BAB8-30EA-4785-8F07-F6E80A053E9D

P932

Q24600920-EE16227D-7998-425F-887B-EF403363F09A

P3181

P356

P1433

Journal of the American Chemical Society

P1476

Enantioselective α-benzylation of aldehydes via photoredox organocatalysis

@en

P2093

David W C MacMillan

http://www.w3.org/2001/XMLSchema#string

Hui-Wen Shih

http://www.w3.org/2001/XMLSchema#string

Mark N Vander Wal

http://www.w3.org/2001/XMLSchema#string

Rebecca L Grange

http://www.w3.org/2001/XMLSchema#string

P2860

Enantioselective alpha-trifluoromethylation of aldehydes via photoredox organocatalysis

[2+2] cycloadditions by oxidative visible light photocatalysis

Crossed intermolecular [2+2] cycloadditions of acyclic enones via visible light photocatalysis

Merging photoredox catalysis with organocatalysis: the direct asymmetric alkylation of aldehydes

Efficient visible light photocatalysis of [2+2] enone cycloadditions

Visible-light photoredox catalysis: aza-Henry reactions via C-H functionalization.

Tin-free radical cyclization reactions initiated by visible light photoredox catalysis.

Recent advances in asymmetric phase-transfer catalysis.

Enantioselective catalytic alpha-alkylation of aldehydes via an SN1 pathway.

Electron transfer photoredox catalysis: intramolecular radical addition to indoles and pyrroles.

P304

13600-3

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

3327340

http://www.w3.org/2001/XMLSchema#string

P356

10.1021/JA106593M

http://www.w3.org/2001/XMLSchema#string

P407

P433

39

http://www.w3.org/2001/XMLSchema#string

P478

132

http://www.w3.org/2001/XMLSchema#string

P577

2010-10-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

46217699

http://www.w3.org/2001/XMLSchema#string

P698

20831195

http://www.w3.org/2001/XMLSchema#string

P921

enantioselectivity

P932

3056320

http://www.w3.org/2001/XMLSchema#string