N-acylsulfonamide assisted tandem C-H olefination/annulation: synthesis of isoindolinones.
about
Synthesis of a library of tricyclic azepinoisoindolinones.Scope and Mechanistic Study of the Coupling Reaction of α, β-Unsaturated Carbonyl Compounds with Alkenes: Uncovering Electronic Effects on Alkene Insertion vs Oxidative Coupling PathwaysRhodium(iii)-catalyzed synthesis of phthalides by cascade addition and cyclization of benzimidates with aldehydes.Ligand-Accelerated ortho-C-H Olefination of Phenylacetic Acids.Amide-directed tandem C-C/C-N bond formation through C-H activation.Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.Heterocycle Formation via Palladium-Catalyzed C-H Functionalization.Rhodium-catalyzed annulation of N-benzoylsulfonamide with isocyanide through C-H activation.Rhodium catalyzed synthesis of isoindolinones via C-H activation of N-benzoylsulfonamides.Alternative pathways for Heck intermediates: palladium-catalyzed oxyarylation of homoallylic alcoholsAerobic oxidative coupling between carbon nucleophiles and allylic alcohols: a strategy to construct β-(hetero)aryl ketones and aldehydes through hydrogen migration.Rh(iii)-catalyzed C-H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant.Catalyst-Free Three-Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer-Type Rearrangement.Ruthenium Oxidase Catalysis for Site-Selective C-H Alkenylations with Ambient O2 as the Sole Oxidant.A tandem Heck-aza-Michael addition protocol for the one-pot synthesis of isoindolines from unprotected amines.Combined electrochemical/chemical methods for the synthesis and the molecular diversifying of isoindolinone-based heterocyclic scaffolds.Synthesis of isoindolinones via palladium-catalyzed C-H activation of N-methoxybenzamides.Palladium-catalyzed C-H activation and intermolecular annulation with allenes.
P2860
Q34423606-D086D618-9AD9-4794-B3B3-5994F67AC849Q35773663-314A82EB-D98E-48F3-89EF-2FDE29BE07EEQ36290673-D90AB761-8212-4DBE-8D13-F8AF9E9E12D8Q37074358-D4BAFE8B-F43A-4B15-AD61-10CFFCB9BF56Q38001646-B629230E-96E0-490C-BFF1-DFEE9CA8BE5CQ38097103-9D465804-23E1-4699-91FF-EF708AF0FF58Q38891800-157972AA-6699-422E-A724-6CA69FEB9740Q42042310-D5AF03E2-B21E-45D7-BF11-20C2CB6106B3Q42269950-947EA264-0B98-407B-9E14-2D7426B0CF1FQ42400769-100DC1C6-D264-4629-9683-73E959AE545EQ46979387-F327A72A-146B-4C52-954F-95848A90581AQ49839379-61D46A20-659B-4720-8124-5AE1D60799AEQ50868024-B790948E-E088-4FD8-A82C-F35A3869B6D5Q50921429-AD031D0F-FD11-4E39-84A0-7264F7F19CE4Q51343820-214F6CB8-EAA2-4C4E-95BB-B804B2D2696AQ51759242-B094D9BA-4055-40A9-A32B-12C83CEAA9F5Q53208539-6EE49A02-A9A7-4C56-B959-507B3153F4BEQ53599806-B4898B8A-552A-4593-AAF9-51ACD7479378
P2860
N-acylsulfonamide assisted tandem C-H olefination/annulation: synthesis of isoindolinones.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@en
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@nl
type
label
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@en
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@nl
prefLabel
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@en
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@nl
P2860
P356
P1433
P1476
N-acylsulfonamide assisted tan ...... : synthesis of isoindolinones.
@en
P2093
P2860
P304
P356
10.1021/OL200093F
P407
P577
2011-02-08T00:00:00Z