Pd-Catalyzed γ-C(sp3)-H Arylation of Free Amines Using a Transient Directing Group.
about
Single operation palladium catalysed C(sp3)-H functionalisation of tertiary aldehydes: investigations into transient imine directing groupsMethylene C(sp3)-H Arylation of Aliphatic Ketones Using a Transient Directing Group.Complementary Strategies for Directed C(sp3 )-H Functionalization: A Comparison of Transition-Metal-Catalyzed Activation, Hydrogen Atom Transfer, and Carbene/Nitrene Transfer.o-Phthalaldehyde catalyzed hydrolysis of organophosphinic amides and other P([double bond, length as m-dash]O)-NH containing compounds.Selective Palladium(II)-Catalyzed Carbonylation of Methylene β-C-H Bonds in Aliphatic Amines.Buttressing Salicylaldehydes: A Multipurpose Directing Group for C(sp3 )-H Bond Activation.Stereoselective Sulfinyl Aniline-Promoted Pd-Catalyzed C-H Arylation and Acetoxylation of Aliphatic Amides.Remote, Late-Stage Oxidation of Aliphatic C-H Bonds in Amide-Containing Molecules.Organocatalysis using aldehydes: the development and improvement of catalytic hydroaminations, hydrations and hydrolyses.Palladium-catalyzed enantioselective C(sp2)-H arylation of ferrocenyl ketones enabled by a chiral transient directing group.Rh(iii)-Catalyzed bilateral cyclization of aldehydes with nitrosos toward unsymmetrical acridines proceeding with C-H functionalization enabled by a transient directing group.sp3 C-H activation via exo-type directing groups.γ-Functionalizations of Amines through Visible-Light-Mediated, Redox-Neutral C-C Bond Cleavage.Sulfinyl isobutyramide as an auxiliary for palladium(ii)-catalyzed C-H arylation and iodination of benzylamine derivatives.Pd(ii)-catalyzed synthesis of bifunctionalized carboranes via cage B-H activation of 1-CH2NH2-o-carboranes.The α-tertiary amine motif drives remarkable selectivity for Pd-catalyzed carbonylation of β-methylene C-H bonds.Oximes as reusable templates for the synthesis of ureas and carbamates by an in situ generation of carbamoyl oximesDiastereoselective C-H carbonylative annulation of aliphatic amines: a rapid route to functionalized γ-lactams
P2860
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P2860
Pd-Catalyzed γ-C(sp3)-H Arylation of Free Amines Using a Transient Directing Group.
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
Pd-Catalyzed γ-C
@nl
Pd-Catalyzed γ-C(sp3)-H Arylation of Free Amines Using a Transient Directing Group.
@en
type
label
Pd-Catalyzed γ-C
@nl
Pd-Catalyzed γ-C(sp3)-H Arylation of Free Amines Using a Transient Directing Group.
@en
prefLabel
Pd-Catalyzed γ-C
@nl
Pd-Catalyzed γ-C(sp3)-H Arylation of Free Amines Using a Transient Directing Group.
@en
P2093
P2860
P356
P1476
Pd-Catalyzed γ-C(sp3)-H Arylation of Free Amines Using a Transient Directing Group.
@en
P2093
Martin D Eastgate
Yan-Qiao Chen
Yongwei Wu
P2860
P304
14554-14557
P356
10.1021/JACS.6B09653
P407
P50
P577
2016-10-27T00:00:00Z