About: Cobalt(II)-Catalyzed Intramolecular C−H Amination with Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidates

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About: Cobalt(II)-Catalyzed Intramolecular C−H Amination with Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidates Goto Sponge NotDistinct Permalink

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scholarly article by Hongjian Lu et al published 19 March 2010 in Organic Letters

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rdf:type	Item
description	наукова стаття, опублікована в березні 2010 (uk) im März 2010 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Hongjian Lu et al published 19 March 2010 in Organic Letters (en)
publication date	wds:Q57834075-A389A969-7BF3-4A81-BEFF-31A711F354DE
publication date	2010-03-19 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57834075-03784EBF-BB2C-45AC-82FF-859F5F5D9DA9
language of work or name	English
author name string	wds:Q57834075-16E5A664-E112-4479-84DF-60D3DC3154EE wds:Q57834075-87792070-5B0C-4241-B567-EBE7F7C95289 wds:Q57834075-E036CFD4-C033-46D5-B02B-9E61B926AA48
author name string	Jingran Tao Hongjian Lu Jess E. Jones
rdfs:label	Cobalt(II)-Catalyzed Intramolecular C−H Amination with Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidates (en)
skos:prefLabel	Cobalt(II)-Catalyzed Intramolecular C−H Amination with Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidates (en)
name	Cobalt(II)-Catalyzed Intramolecular C−H Amination with Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidates (en)
author	wds:Q57834075-863CFEC5-BA8B-452E-A3B7-0D8243EA4769 wds:Q57834075-E7CCC4BD-C0FC-448E-8AB7-40AF3DEE5EE0
author	Peter Zhang Lukasz Wojtas
title	wds:Q57834075-8775CB10-BE0A-43BA-A381-C184069ED617
title	Cobalt(II)-Catalyzed Intramolecular C−H Amination with Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidates (en)
page(s)	wds:Q57834075-E53955B0-6E5F-4A02-A5A2-CFD60BAB8419
page(s)	1248-1251
instance of	wds:Q57834075-EC56BB05-B9A5-4FF8-965B-7059F78555B7
instance of	scholarly article
main subject	wds:Q57834075-798ff966-e8b5-4360-adc3-f0e1cbd37505
main subject	cobalt
PubMed ID	wds:Q57834075-E882F8E8-E3FE-4FE3-BA6C-84C63DFC5826
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20184343
PubMed ID	20184343
published in	wds:Q57834075-D5C55779-BF68-4709-AD22-A7CF1833BB3B
published in	Organic Letters
issue	wds:Q57834075-753ED89D-A855-4314-B9AE-8F086CDDE98C
volume	wds:Q57834075-9BC50C43-1AF1-4554-B906-16957E434642
issue	6
volume	12
DOI	wds:Q57834075-EBC4498B-CE3D-4203-8770-D3C45D7E0AD5
DOI	http://dx.doi.org/10.1021/OL100110Z
DOI	10.1021/OL100110Z
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57834075
is cites work of	Recent advances in transition metal-catalyzed N-atom transfer reactions of azides Rh2(II)-catalyzed intramolecular aliphatic C-H bond amination reactions using aryl azides as the N-atom source Iron(II) bromide-catalyzed intramolecular C-H bond amination [1,2]-shift tandem reactions of aryl azides Selective Radical Amination of Aldehydic C(sp(2))-H Bonds with Fluoroaryl Azides via Co(II)-Based Metalloradical Catalysis: Synthesis of N-Fluoroaryl Amides from Aldehydes under Neutral and Nonoxidative Conditions Selective functionalisation of saturated C-H bonds with metalloporphyrin catalysts Enantio- and regioselective intermolecular benzylic and allylic C-H bond amination. Cobalt-Catalyzed, Aminoquinoline-Directed Functionalization of Phosphinic Amide sp2 C-H Bonds. Ruthenium-catalyzed γ-carbolinium ion formation from aryl azides; synthesis of dimebolin Rhodium-catalyzed synthesis of 2,3-disubstituted indoles from β,β-disubstituted stryryl azides Catalytic C-H functionalization by metalloporphyrins: recent developments and future directions Complexes with nitrogen-centered radical ligands: classification, spectroscopic features, reactivity, and catalytic applications The radical mechanism of cobalt(II) porphyrin-catalyzed olefin aziridination and the importance of cooperative H-bonding. Stereoselective radical amination of electron-deficient C(sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination Iron-catalyzed C-H and C-C bond cleavage: a direct approach to amides from simple hydrocarbons. Chemoselective intramolecular allylic C–H amination versus CC aziridination through Co(ii)-based metalloradical catalysis Characterization of Porphyrin-Co(III)-'Nitrene Radical' Species Relevant in Catalytic Nitrene Transfer Reactions Metal-Catalyzed and Metal-Free Intermolecular Amination of Light Alkanes and Benzenes Asymmetric nitrene transfer reactions: sulfimidation, aziridination and C-H amination using azide compounds as nitrene precursors. Chemoselective amination of propargylic C(sp³)-H bonds by cobalt(II)-based metalloradical catalysis Cobalt catalyzed sp3 C-H amination utilizing aryl azides. Homolytic N-H activation of ammonia: hydrogen transfer of parent iridium ammine, amide, imide, and nitride species Catalytic Synthesis of N-Heterocycles via Direct C(sp3)-H Amination Using an Air-Stable Iron(III) Species with a Redox-Active Ligand Nitrene Radical Intermediates in Catalytic Synthesis 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). Insights into the Mechanism of the Ruthenium-Porphyrin-Catalysed Allylic Amination of Olefins by Aryl Azides Palladium-catalyzed, aminoquinoline-directed arylation of phosphonamidate and phosphinic amide sp3 C-H bonds. Intramolecular Radical Aziridination of Allylic Sulfamoyl Azides by Cobalt(II)-Based Metalloradical Catalysis: Effective Construction of Strained Heterobicyclic Structures Intramolecular 1,5-C(sp3)-H Radical Amination via Co(II)-Based Metalloradical Catalysis for Five-Membered Cyclic Sulfamides Catalytic Radical Process for Enantioselective Amination of C(sp3)-H Bonds Ruthenium porphyrins-catalyzed atom-efficient amination of C-H bonds by arylazides Enantioselective intramolecular C-H amination of aliphatic azides by dual ruthenium and phosphine catalysis One-Pot Synthesis of P()-N Containing Compounds Using -Chlorosuccinimide and Their Influence in Thermal Decomposition of PU Foams [Ru(TPP)CO]-Catalysed Intramolecular Benzylic CH Bond Amination, Affording Phenanthridine and Dihydrophenanthridine Derivatives Application of [Co(Corrole)]- Complexes in Ring-Closing C-H Amination of Aliphatic Azides via Nitrene Radical Intermediates Comparative Study of the Catalytic Amination of Benzylic C-H Bonds Promoted by Ru(TPP)(py)2and Ru(TPP)(CO)
is cites work of	wds:Q36098151-DDAAA7AC-D976-461C-831A-B3547A4EA9A4 wds:Q42764343-0A4DEE13-5953-4DA9-8763-622AAAF44F4F wds:Q41533589-3F77EBFF-3722-4018-8E71-A37E7C14E1F5 wds:Q42061881-2AC607A9-978C-4F27-BEBE-63A42F1BE57C wds:Q46943397-604BD10A-28DC-4207-9840-79033108A1F9 wds:Q49466223-A69FF4D3-F3C8-40B3-BBDB-D3AF73E8A08E wds:Q43129522-CAE0FCB3-F80C-4D75-A301-95AD7814EB13 wds:Q55076303-E0EF9E6F-24F7-49AE-A5C9-CCB7AAA19429 wds:Q57800789-C8577F9F-61E0-427F-A08F-5C1D53C4A96F wds:Q59079550-2DCECD74-2F9A-4338-A212-F90EC12F8C76 wds:Q64275301-20E513F2-F1FD-4BF4-BD2C-F7115142BA55 wds:Q38161491-2AF0CCFE-A731-4709-B0A1-669CF9982918 wds:Q36570787-3C251C77-ED2C-4413-AF5A-EB54F773A383 wds:Q38905373-12282FE8-24F8-45AF-9012-F875B1F0DCC5 wds:Q42327546-E856048B-4E35-40B3-9405-152F8D9DA455 wds:Q41036037-07DF4748-E074-44B4-96F5-7E72A662A139 wds:Q56740156-D1C05B58-06BB-401C-A91A-642574E63AD5 wds:Q57834047-AC58001F-EE51-4F44-BA9E-CC3F43C24C51 wds:Q54771939-3460DD85-4D0B-4458-8029-FEDBFC33EE4B wds:Q34989553-1A8CF5B3-F8E2-4D2B-8049-5A5406AC2B80 wds:Q37810785-76CFC379-D68D-4330-9DBF-87518F378210 wds:Q42453687-646BDE08-82C9-489A-88D1-AF1D314ED833 wds:Q46591390-5B7592E3-370B-4C34-8C48-BCB543302186

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