Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
about
Azidation in the Difunctionalization of OlefinsProduct-Derived Bimetallic Palladium Complex Catalyzes Direct Carbonylation of Sulfonylazides.Characterization of Porphyrin-Co(III)-'Nitrene Radical' Species Relevant in Catalytic Nitrene Transfer Reactions.Catalytic Synthesis of N-Heterocycles via Direct C(sp3)-H Amination Using an Air-Stable Iron(III) Species with a Redox-Active Ligand.Transition-Metal-Catalyzed Electrophilic Amination: Application of O-Benzoylhydroxylamines in the Construction of the C-N Bond.Metal-Catalysed Azidation of Organic MoleculesA mechanistic investigation of the ruthenium porphyrin catalysed aziridination of olefins by aryl azides.Cobalt-Porphyrin-Catalysed Intramolecular Ring-Closing C-H Amination of Aliphatic Azides: A Nitrene-Radical Approach to Saturated Heterocycles.Catalytic C-H amination driven by intramolecular ligand-to-nitrene one-electron transfer through a rhodium(iii) centre.C-H functionalization by high-valent Cp*Co(iii) catalysis.Porphyrin Cobalt(III) "Nitrene Radical" Reactivity; Hydrogen Atom Transfer from Ortho-YH Substituents to the Nitrene Moiety of Cobalt-Bound Aryl Nitrene Intermediates (Y = O, NH).Tandem Coupling of Azide with Isonitrile and Boronic Acid: Facile Access to Functionalized Amidines.Transition metal-catalyzed iodine(iii)-mediated nitrene transfer reactions: efficient tools for challenging syntheses.Elusive Terminal Copper Arylnitrene Intermediates.Highly Stable Mesoporous Zirconium Porphyrinic Frameworks with Distinct Flexibility.Multi-electron redox processes at a Zr(iv) center facilitated by an appended redox-active cobalt-containing metalloligand.Pd(II) -Catalyzed Intermolecular Amination of Unactivated C(sp(3) )-H Bonds.Iridium(III)-Catalyzed Benzylic Amine Directed CH Sulfonamidation of Arenes with Sulfonyl AzidesRecent advances in C–H bond aminations catalyzed by ruthenium porphyrin complexesSynthesis in mesoreactors: Ru(porphyrin)CO-catalyzed aziridination of olefins under continuous flow conditions
P2860
Q26753058-D7D3B0BE-8D9C-497F-9CFA-8963D3690377Q33467531-04A7EAF1-1C17-4680-A73F-ED7698642EF2Q36570787-2FF95CE0-1526-4D9C-BA6F-F76E41F5ECA9Q38905373-2A892137-6D9F-4D32-B749-5445682B9789Q38908370-2FEDC4E5-F333-4832-8C2A-671A18A1EE61Q39201456-0D11BFB3-AC16-4FCF-9FD2-C8C578FD14B1Q40935689-FE9D2CAC-288B-4B6A-8D99-63343D69DBCCQ41019640-625F9918-5DF7-47F3-BCB1-C94EFE0B1F69Q46381118-464BCFF5-5AC0-43AA-A053-EC5FBD3FC3ACQ46409049-6DE9242F-F790-45A6-AC0C-FD715636430EQ46591390-6376A2E5-06D4-4E36-8476-276116CE3A05Q48102948-00DF6374-E850-4DCA-BFBC-39B164F51E1BQ48184302-4D23A6DE-758C-45B8-AEC8-D207BA85255FQ48192900-1BA588B1-BD35-43E5-BF85-1B4F49670914Q51456126-80C77119-3C70-42F6-857D-295FDFD7E4DCQ53037108-002B3CA1-0ABE-47EC-A395-1BC6A69E84E1Q53354833-1450259E-2715-4FA5-8706-93B0C404CDF6Q57864637-27F83CB8-5993-4BC3-B26C-88454CADC636Q59078892-9DE98BD8-39B3-447F-9984-F74F5BFF538BQ59078931-86123EAC-046A-4745-A1CF-8C6D5CAEA6F1
P2860
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@en
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@nl
type
label
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@en
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@nl
prefLabel
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@en
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@nl
P2860
P50
P356
P1476
Organic azides: "energetic reagents" for the intermolecular amination of C-H bonds.
@en
P2093
Daniela Intrieri
P2860
P304
11440-11453
P356
10.1039/C4CC03016H
P407
P577
2014-10-01T00:00:00Z