about
Current status and future prospects for enabling chemistry technology in the drug discovery processOxazolines as Dual-Function Traceless Chromophores and Chiral Auxiliaries: Enantioselective Photoassisted Synthesis of Polyheterocyclic Ketones.Asymmetric Radical Cyclopropanation of Alkenes with In Situ-Generated Donor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis.Asymmetric copper-catalyzed C-N cross-couplings induced by visible lightCyclobutane and cyclobutene synthesis: catalytic enantioselective [2+2] cycloadditions.Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions.Dual Catalysis Strategies in Photochemical Synthesis.Studies in organic and physical photochemistry - an interdisciplinary approach.Enantioselective photochemistry through Lewis acid-catalyzed triplet energy transferEnantioselective Organocatalytic Diels-Alder Trapping of Photochemically Generated Hydroxy-o-Quinodimethanes.Exploiting Octahedral Stereocenters: From Enzyme Inhibition to Asymmetric Photoredox Catalysis.Photo-organocatalytic Enantioselective Perfluoroalkylation of β-Ketoesters.Cyclobutene vs 1,3-Diene Formation in the Gold-Catalyzed Reaction of Alkynes with Alkenes: The Complete Mechanistic Picture.A Chiral Thiourea as a Template for Enantioselective Intramolecular [2 + 2] Photocycloaddition Reactions.Tunable chiral metal organic frameworks toward visible light-driven asymmetric catalysis.A Conjugated Microporous Polymer for Palladium-Free, Visible Light-Promoted Photocatalytic Stille-Type Coupling Reactions.Enantioselective Photocatalytic [3 + 2] Cycloadditions of Aryl Cyclopropyl Ketones.Mechanism of the Stereoselective α-Alkylation of Aldehydes Driven by the Photochemical Activity of Enamines.Trifluoroethoxy-Coated Subphthalocyanine affects Trifluoromethylation of Alkenes and Alkynes even under Low-Energy Red-Light Irradiation.Photoredox radical conjugate addition of dithiane-2-carboxylate promoted by an iridium(iii) phenyl-tetrazole complex: a formal radical methylation of Michael acceptors.Synthesis of 1,3-Substituted Cyclobutanes by Allenoate-Alkene [2 + 2] Cycloaddition.Enantioselective Intermolecular [2 + 2] Photocycloaddition Reactions of 2(1H)-Quinolones Induced by Visible Light Irradiation.Light-Driven Enantioselective Organocatalytic β-Benzylation of Enals.Brønsted Acid Catalysis in Visible-Light-Induced [2+2] Photocycloaddition Reactions of Enone Dithianes.Photochemical Stereocontrol Using Tandem Photoredox-Chiral Lewis Acid Catalysis.Forging Fluorine-Containing Quaternary Stereocenters by a Light-Driven Organocatalytic Aldol Desymmetrization ProcessVisible-Light-Mediated Generation of Nitrogen-Centered Radicals: Metal-Free Hydroimination and Iminohydroxylation Cyclization Reactions.Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones.Combining the catalytic enantioselective reaction of visible-light-generated radicals with a by-product utilization system.Organocatalytic Enantioselective Protonation for Photoreduction of Activated Ketones and Ketimines Induced by Visible Light.Harnessing sunlight without a photosensitizer for highly efficient consecutive [3+2]/[4+2] annulation to synthesize fused benzobicyclic skeletons.Structural Design Principle of Small-Molecule Organic Semiconductors for Metal-Free, Visible-Light-Promoted Photocatalysis.Evidence for Triplet Sensitization in the Visible-Light-Induced [2+2] Photocycloaddition of Eniminium Ions.Enantioselective Excited-State Photoreactions Controlled by a Chiral Hydrogen-Bonding Iridium Sensitizer.Strategies to diversify natural products for drug discovery.Enantioselective Photochemical Organocascade Catalysis.Realizing an Aza Paternò-Büchi Reaction.An Aminocatalyzed Stereoselective Strategy for the Formal α-Propargylation of Ketones.Visible-Light-Promoted Asymmetric Cross-Dehydrogenative Coupling of Tertiary Amines to Ketones by Synergistic Multiple Catalysis.A Chiral Metal Photocatalyst Architecture for Highly Enantioselective Photoreactions.
P2860
Q28066266-EF2983A4-CCA3-4A97-87B9-3F2A2C86A2BCQ30384326-75C20B89-6263-4E1E-A848-B4F96D7E0DF3Q34548536-76AE1F98-54B7-448F-872D-C3458E1A92C3Q36628980-A86FE38C-F423-4AF4-A01C-94ECAFDE29B3Q38579261-C2952701-D96B-42A7-9CB3-94A8F6C5BFF7Q38790718-72718348-1A44-412E-A25F-E954B39DF6F6Q38816266-06BD1927-AB42-4B23-84BC-C2DD25EC887FQ38887121-22815400-AA6F-4647-878B-1C9FABD51964Q39097130-BE7380C1-7F63-4C68-958E-61D1C3A4CA0BQ39152625-B15F0AFD-1829-4A6B-919C-34E68A499F3BQ39192964-B9138C5A-F419-4ADC-85DC-2838DD48B361Q40555683-3905B031-5A9E-4A4A-A990-16E09F21441DQ41246705-1D259D95-E2C0-4B56-AA37-A612F025E6D8Q41428802-E54137A0-8F02-4DFC-A202-4A9C77F50D2BQ41456802-BA75D92C-DF69-43B0-B285-B9294A1AE218Q41483322-D79EF2D8-65D0-48AB-90A2-B57C941AD4A7Q41504899-084AD040-F23B-42C4-A611-C1A0875972ACQ42013059-8676AEF0-B125-4E18-9A6A-142042ECC3A0Q42013837-25EC0239-3506-4254-B928-E78EF9928644Q42035035-840BCE85-267F-4383-940F-97B2B2FE464AQ42058114-C5687DFD-2D7E-4F86-BCDF-B048268F02CFQ42071641-3515460E-EE4E-4ECF-B780-2852184CA678Q42150423-FE8E3BB2-BFED-4E83-8805-E995A114526DQ42291073-546C6AA6-C0EE-470A-9B96-B22A1F5FB38BQ42379295-B45387D1-7DC0-4FD1-9DD6-74BFA948F715Q42703521-2C9661E0-86CD-4448-AB1D-3B77EE6064A1Q43170725-F3926B95-D62D-452E-B3D9-A8E918453E9DQ47375255-132C7FBA-10F9-4797-B0DA-ACF5FDF3376EQ47385464-956ED0EF-8B7E-49C0-A563-74B9952FFFFEQ47660917-4269471B-C62A-48FD-9FDC-8D93CC8DA6A2Q47671813-59F00A13-5388-445B-BF28-85166473347FQ48041644-9D1B16BF-53A4-498A-BEE9-A18906C6EEBBQ48047990-AD53AF4C-C127-4EBC-9C36-AB5D92289B13Q48050267-1876E865-8145-4FA9-B405-A9705C7F7759Q48138855-FC93BE63-C177-41FF-8CA3-C445E2446E37Q48178602-694E4B8F-A249-4A25-AE2F-3BA94CE519F0Q48220143-052CC6F6-17A6-482B-8337-9A6F877FA589Q48220229-6C87E910-DE2B-4788-9DF6-A688A3FBAAF5Q48224035-DF9A26BA-CA33-4E36-B470-0F0BDC53487CQ48256102-2F3E036F-A543-46DE-B2E7-457AFFC18C0C
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Enantioselective catalysis of photochemical reactions.
@en
type
label
Enantioselective catalysis of photochemical reactions.
@en
prefLabel
Enantioselective catalysis of photochemical reactions.
@en
P2860
P356
P1476
Enantioselective catalysis of photochemical reactions.
@en
P2093
Dominik Lenhart
Richard Brimioulle
P2860
P304
P356
10.1002/ANIE.201411409
P407
P577
2015-02-27T00:00:00Z