about
Palladium-Catalyzed, Site-Selective Direct Allylation of Aryl C-H Bonds by Silver-Mediated C-H Activation: A Synthetic and Mechanistic Investigation.Direct Assembly of Prenylated Heteroarenes through a Cascade Minisci Reaction/Dehydration Sequence.Structures, Reactions, and Mechanisms: Stereochemistry in the Broadest Sense at the 51st Bürgenstock Conference.Unprecedented selective homogeneous cobalt-catalysed reductive alkoxylation of cyclic imides under mild conditions.Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reactionManganese-catalyzed allylation via sequential C-H and C-C/C-Het bond activation.Manganese(I)-Catalyzed C-H Activation: The Key Role of a 7-Membered Manganacycle in H-Transfer and Reductive EliminationAromatic C-H addition of ketones to imines enabled by manganese catalysis.Manganese-catalyzed synthesis of monofluoroalkenes via C-H activation and C-F cleavage.Heteromultimetallic catalysis for sustainable organic syntheses.Manganese(I)-Catalyzed Dispersion-Enabled C-H/C-C Activation.MnCl2 -Catalyzed C-H Alkylations with Alkyl Halides.Manganese(I)-Catalyzed C-H (2-Indolyl)methylation: Expedient Access to Diheteroarylmethanes.Air-Stable Manganese(I)-Catalyzed C-H Activation for Decarboxylative C-H/C-O Cleavages in Water.Polycyclization Enabled by Relay Catalysis: One-Pot Manganese-Catalyzed C-H Allylation and Silver-Catalyzed Povarov Reaction.Manganese-Catalyzed C-H Functionalizations: Hydroarylations and Alkenylations Involving an Unexpected Heteroaryl Shift.Redox-Neutral Manganese(I)-Catalyzed C-H Activation: Traceless Directing Group Enabled Regioselective Annulation.Full Selectivity Control in Cobalt(III)-Catalyzed C-H Alkylations by Switching of the C-H Activation Mechanism.Manganese-Catalyzed C-H Alkynylation: Expedient Peptide Synthesis and Modification.Methylenecyclopropane Annulation by Manganese(I)-Catalyzed Stereoselective C-H/C-C Activation.Highly Selective Manganese(I)/Lewis Acid Cocatalyzed Direct C-H Propargylation Using Bromoallenes.N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.Temperature-controlled redox-neutral ruthenium(ii)-catalyzed regioselective allylation of benzamides with allylic acetates.Synergistic Heterobimetallic Manifold for Expedient Manganese(I)-Catalyzed C-H Cyanation.Catalyst-Guided C=Het Hydroarylations by Manganese-Catalyzed Additive-Free C-H Activation.Dual vicinal functionalisation of heterocycles via an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade.C4-H indole functionalisation: precedent and prospects.Mangan(I)-katalysierte C-H-(2-Indolyl)methylierung: ein einfacher Zugang zu Diheteroarylmethan-DerivatenHochselektive Mangan(I)/Lewis-Säure-cokatalysierte direkte C-H-Propargylierung unter Verwendung von BromallenenRedoxneutrale Mangan(I)-katalysierte C-H-Aktivierung: regioselektive Anellierung mithilfe einer spurlosen dirigierenden GruppeMangan(I)-katalysierte regioselektive C-H-Allenierung: direkte Synthese von 2-AllenylindolenMethylenecyclopropane Annulation by Manganese(I)-Catalyzed Stereoselective C−H/C−C ActivationFull Selectivity Control in Cobalt(III)-Catalyzed C−H Alkylations by Switching of the C−H Activation MechanismAir-Stable Manganese(I)-Catalyzed C−H Activation for Decarboxylative C−H/C−O Cleavages in WaterManganese-Catalyzed C−H Alkynylation: Expedient Peptide Synthesis and ModificationRhodium-Catalyzed Alkenyl C−H Activation and Oxidative Coupling with Allylic Alcohols
P2860
Q37510346-2AB6513A-0DF3-4AC1-8D64-E6A2656C9AEAQ37515407-07C845E7-5F5C-480E-A7B9-15955CDE5E9DQ38874436-01481A10-6734-443E-A1C1-8831C80D0B1DQ41830943-FA38F86E-4450-45AF-9255-462C2496BC8CQ41889268-A2E374DE-101B-4A99-87DA-86BF84AEBB5FQ42289681-73540288-BC5A-457F-B2BF-0AB95A895ED9Q42366811-FCC14D98-5EB3-4604-B423-749C6DFB257BQ42611738-72F8DA3A-C63E-4B85-9E10-55D68D151FE4Q47903493-140E8E64-1BA3-4452-A0F8-897EEA9C746AQ48051193-72E07EF1-FFEF-4E65-8578-BC2CA98F0103Q48105896-C0604CB1-FDA9-496C-A196-7F448D41713FQ48130351-BFCF546C-5F4A-4CA7-BF97-F0959362D4D5Q48178614-FB3AB229-85AB-4B9D-99FD-9C343D2D0584Q48186527-02FA1FA6-1A1B-4B45-9164-0466019B192AQ48191916-4D72CEEC-F4EA-4CF6-83EE-AC73AC8FEC1AQ48227411-5FEFF4FB-B02B-4B4A-88AD-713C559205C1Q48237495-8D92E632-A372-4964-B591-133002A73E0EQ48245200-0F99B3E5-B251-436F-9986-23CD0B23FD11Q48257765-A5231173-A73E-449A-A710-D44C59A613D0Q48292264-FFF32B93-E767-4C6E-9CCD-127BCCA9983BQ48298995-B13063F9-BFE1-4DB6-9638-8C45036E17E3Q48355121-29CA190B-B2A6-4D84-8A4C-DC35C2BC2666Q52985877-5098514A-792F-406E-B321-2B5D14F93781Q53792988-42218BDA-9331-4BBB-BB4C-C277C3A04B02Q54508598-983C4A86-0FCF-4FCF-8832-4631CEA9487DQ55058175-D6149857-4638-48A5-AD88-11D468C21B89Q55447796-E86F9EF3-77C4-4FEF-8893-7261AF075460Q57656869-479061D5-CE33-4198-8582-4683B6CCC301Q57656874-F5249E93-1FC9-47CD-A2CF-472C4B1B9337Q57656897-30A70862-09DB-4F3E-97D0-187E98C2018FQ57656922-7AF56E84-A859-4500-BB5B-498AC6D57C2BQ57905591-0A00D373-DAE0-4D3F-9CDC-E18B15597787Q58656139-89D07818-3007-4A4B-8C9D-9E9B1C336A6AQ58656146-94C5886F-BCAC-4816-8CCA-2B81CF277168Q58656155-DCCB58DD-3D2F-4A9F-85EF-8CCAF6199B77Q58830143-B8E472FF-8F08-4674-ABDE-CDBE47F5CCB1
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-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
2016年學術文章
@zh-hant
name
Manganese(I)-Catalyzed Substitutive C-H Allylation.
@en
type
label
Manganese(I)-Catalyzed Substitutive C-H Allylation.
@en
prefLabel
Manganese(I)-Catalyzed Substitutive C-H Allylation.
@en
P2093
P2860
P356
P1476
Manganese(I)-Catalyzed Substitutive C-H Allylation.
@en
P2093
Lutz Ackermann
Sven C Richter
Yujiao Zhang
P2860
P304
P356
10.1002/ANIE.201601560
P407
P50
P577
2016-04-20T00:00:00Z