about
Chemoselective single-site Earth-abundant metal catalysts at metal-organic framework nodesCopper-catalyzed oxidative amination and allylic amination of alkenes.Direct nitration and azidation of aliphatic carbons by an iron-dependent halogenaseIntramolecular C(sp(3))H amination of arylsulfonyl azides with engineered and artificial myoglobin-based catalysts.Enzyme-controlled nitrogen-atom transfer enables regiodivergent C-H amination.An expedient synthesis of maraviroc (UK-427,857) via C-H functionalization.Tuning the Reactivity of Radical through a Triplet Diradical Cu(II) Intermediate in Radical Oxidative Cross-CouplingCatalytic enantioselective allylic amination of unactivated terminal olefins via an ene reaction/[2,3]-rearrangementCafestol to Tricalysiolide B and Oxidized Analogues: Biosynthetic and Derivatization Studies Using Non-heme Iron Catalyst Fe(PDP).Iron(II) bromide-catalyzed intramolecular C-H bond amination [1,2]-shift tandem reactions of aryl azides.P450-catalyzed intramolecular sp(3) C-H amination with arylsulfonyl azide substrates.Sequential catalysis for stereoselective synthesis of complex polyketides.Tunable differentiation of tertiary C-H bonds in intramolecular transition metal-catalyzed nitrene transfer reactions.Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes.Iron-Catalyzed C-H Functionalization Processes.Triiodide-Mediated δ-Amination of Secondary C-H Bonds.Direct Functionalization of C-H Bonds by Iron, Nickel, and Cobalt Catalysis.A manganese catalyst for highly reactive yet chemoselective intramolecular C(sp(3))-H amination.Tunable, chemoselective amination via silver catalysis.Chemoselective allene aziridination via Ag(I) catalysisMetal-Catalyzed and Metal-Free Intermolecular Amination of Light Alkanes and BenzenesIron(II)-catalyzed intermolecular amino-oxygenation of olefins through the N-O bond cleavage of functionalized hydroxylamines.Formal synthesis of (-)-agelastatin A: an iron(II)-mediated cyclization strategy.A Highly Selective Vanadium Catalyst for Benzylic C-H Oxidation.Intramolecular 1,5-C(sp3)-H Radical Amination via Co(II)-Based Metalloradical Catalysis for Five-Membered Cyclic Sulfamides.Sequential allylic C-H amination/vinylic C-H arylation: a strategy for unnatural amino acid synthesis from α-olefins.Ligand-controlled, tunable silver-catalyzed C-H amination.Metal-free, highly efficient organocatalytic amination of benzylic C-H bonds.Complex N-heterocycle synthesis via iron-catalyzed, direct C-H bond amination.Recyclable Mitsunobu reagents: catalytic Mitsunobu reactions with an iron catalyst and atmospheric oxygen.Ketimido metallophthalocyanines: an approach to phthalocyanine-supported mononuclear high-valent ruthenium complexes.An artificial metalloenzyme with the kinetics of native enzymes.Computational Investigation of the Role Played by Rhodium(V) in the Rhodium(III)-Catalyzed ortho-Bromination of Arenes.Tandem Oxidative Derivatization of Nitrene Insertion Products for the Highly Diastereoselective Synthesis of 1,3-aminoalcohols.Iron-Catalyzed Intramolecular Aminations of C(sp3 )-H Bonds in Alkylaryl Azides.Direct Catalytic Synthesis of Unprotected 2-Amino-1-Phenylethanols from Alkenes by Using Iron(II) Phthalocyanine.Visible-Light-Induced Direct Oxidative C-H Amidation of Heteroarenes with Sulfonamides.Catalytic C(sp3)-H Alkylation via an Iron Carbene Intermediate.[Fe(F20 TPP)Cl]-catalyzed amination with arylamines and {[Fe(F20 TPP)(NAr)](PhI=NAr)} + . Intermediate assessed by high-resolution ESI-MS and DFT calculations.Metal-Free Ring-Expansion Reaction of Six-membered Sulfonylimines with Diazomethanes: An Approach toward Seven-Membered Enesulfonamides.
P2860
Q28831155-383F2174-5087-4D27-8310-BDF08E028670Q33687697-07E8C596-BF1F-4353-865D-1FB65CEA8187Q33826431-84D8C690-A079-41E9-8016-A4BA81919B51Q34276305-A88FD0E6-5338-4042-8608-FEAF6FA3D352Q34489542-4AE58418-0A31-41AB-8EEA-2536CF4D0E6AQ35770826-93F700F7-11C4-4732-A77D-A9DFEFA9C50CQ36242189-399D1D5D-1913-4E3F-8057-11F93633076CQ36439018-0453F8B5-C920-49BC-80CB-2CBD65F2AE2FQ36754666-C5A79FF7-71E0-4507-AC24-BCB56BE8FD9BQ36754682-C1D866D6-BEA7-49A5-A49F-DDB6325B6BA9Q37630464-F38FFA87-32AC-42C9-B007-4EB8D2334FEEQ38173242-3AE2498A-761D-4262-AC1B-05D97D25A2A9Q38736359-1F7F6088-E957-4E23-AB14-D1E1348803ADQ38736922-9B29F28D-1DE1-4353-B979-F48F69941F04Q38940419-935B6CE7-5B06-4508-8F97-0C4FAEA92A82Q39329176-BBBC5B1A-FA0E-47C7-BFD7-67E21F67B23CQ39357042-51BE577E-CE19-4757-B5F4-EBF4D4084DC4Q40357253-42831828-DB07-4F52-AE43-971B4F3F3485Q41370449-778BA186-BC2C-41EE-B364-695DAF1EFD52Q41446218-8669A638-3FBB-499E-8626-069F8958E6D7Q41533589-F4FE2F3D-04E5-4262-811E-B0F598E36A2AQ41856039-180AC8B8-8CAB-4B5A-B76B-52C96A076439Q42149162-D1986A46-F0EF-4364-B965-515057ED1078Q42202343-9F591A23-A052-498E-A362-B63579D7B62BQ42327546-64404207-95CF-4DD6-BD15-42D585976A07Q42741143-BA8570B8-0506-43F2-834C-2BEC3D6F7EF3Q43082425-5D5E9B94-ADD9-44C9-9AEB-FAA6CFD8AF43Q43617826-22F82EED-8522-46A3-9B44-ADB71920BBBBQ45137871-4A015ACA-7476-4781-BC4D-6B1695A80AF5Q45744479-EA1A9B76-9C0E-48E0-85C6-4F4F796D92E2Q45968419-FF80E1CF-6255-4B87-A93C-570E57CEC516Q46134477-6973C82C-080B-4948-BE46-D0AB6F3D27C5Q46442865-E7775315-3A55-48DA-ABFE-AC71DF42F736Q48169167-59E0428D-08EC-457C-BB9E-E4962FE613B0Q48180171-94BF25DF-230B-4E1F-A292-01716C88B938Q48249011-DCFC3475-88FB-491D-9E57-0B212BC39E42Q48293278-A260F725-27F3-416E-AB72-29518B38E46DQ48362392-D356B26E-9640-4718-8002-911F858BD18BQ51055047-3CDB8F2A-2CC4-439C-A34D-F8FB47547F99Q51607881-FBE80AF1-75E5-4815-8693-935F7B567792
P2860
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Iron-catalyzed intramolecular allylic C-H amination.
@ast
Iron-catalyzed intramolecular allylic C-H amination.
@en
Iron-catalyzed intramolecular allylic C-H amination.
@nl
type
label
Iron-catalyzed intramolecular allylic C-H amination.
@ast
Iron-catalyzed intramolecular allylic C-H amination.
@en
Iron-catalyzed intramolecular allylic C-H amination.
@nl
prefLabel
Iron-catalyzed intramolecular allylic C-H amination.
@ast
Iron-catalyzed intramolecular allylic C-H amination.
@en
Iron-catalyzed intramolecular allylic C-H amination.
@nl
P356
P1476
Iron-catalyzed intramolecular allylic C-H amination
@en
P2093
M Christina White
P304
P356
10.1021/JA211600G
P407
P577
2012-01-23T00:00:00Z