About: Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill

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About: Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill Goto Sponge NotDistinct Permalink

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scientific article published on 18 December 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у 2008 (uk) article scientifique publié en 2007 (fr) im Dezember 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 18 December 2007 (en) artículu científicu espublizáu n'avientu de 2007 (ast)
publication date	wds:Q57614691-76A7E86A-EB64-4395-B1C9-7F9FC2132081
publication date	2007-12-18 00:00:00Z (xsd:dateTime)
cites work	wds:Q57614691-058AB9E1-4B81-4966-895E-935B43E304C0 wds:Q57614691-154C6E77-0AB4-407C-82FE-954C4A7A1E7B wds:Q57614691-525D4521-4D9A-41A7-8647-575862C79625 wds:Q57614691-5C6E8235-4CD8-4025-ACD8-B65892B37EFD wds:Q57614691-85BA02F9-45D1-4F6E-8E1C-ACE06069215C wds:Q57614691-8E537F0A-D171-4D75-9214-35081EBA57BB wds:Q57614691-8F9FE523-4956-458E-B63A-63EC16C2B026 wds:Q57614691-901A2A47-24C8-40C3-A28C-726ACFD337A8 wds:Q57614691-A0FE63DA-F377-4804-B162-667E99101BE1 wds:Q57614691-A9725476-5621-41B7-885A-6DCE4EEDBEFC wds:Q57614691-AE5C6769-64C8-4CC2-99F5-E438732313FD wds:Q57614691-D3BAE77C-F257-4A4F-B29B-A8CB7560A13A wds:Q57614691-FBBDFB17-023F-40C2-986D-8A8ABDA211F6
cites work	A short enantioselective pathway for the synthesis of the anti-influenza neuramidase inhibitor oseltamivir from 1,3-butadiene and acrylic acid Copper-catalyzed aminohalogenation using the 2-NsNCl(2)/2-NsNHNa combination as the nitrogen and halogen sources for the synthesis of anti-alkyl 3-chloro-2-(o-nitrobenzenesulfonamido)-3-arylpropionates Solvent-Free Carbon-Carbon Bond Formations in Ball Mills Aminochlorination in water: first Brønsted acid-promoted synthesis of vicinal chloramines. Solid-state radical reactions of 1,3-cyclohexanediones with in situ generated imines mediated by manganese(III) acetate under mechanical milling conditions FeCl3-Catalyzed aminohalogenation of arylmethylenecyclopropanes and arylvinylidenecyclopropanes and corresponding mechanistic studies. Mechanochemical Aminochlorination of Electron-Deficient Olefins with Chloramine-T Promoted by (Diacetoxyiodo)benzene Solvent-free mechanochemical and one-pot reductive benzylizations of malononitrile and 4-methylaniline using Hantzsch 1,4-dihydropyridine as the reductant Efficient aziridination of olefins catalyzed by mixed-valent dirhodium(II,III) caprolactamate. Unprecedented CO2-promoted aminochlorination of olefins with Chloramine-T. Aminobromination of Unsaturated Phosphonates Die addition von cyanamid und halogen an olefine ein neues verfahren zur darstellung von vic.-halogencyanaminen und aziridinen CuCl-Catalyzed Regio- and Stereoselective Aminohalogenation of α,β-Unsaturated Nitriles
author name string	wds:Q57614691-740264A4-76FA-4207-9125-227ABC094F0B wds:Q57614691-9509FECE-8D41-4B9E-886F-3615B854E15D
author name string	Jing-Jing Xia Xue-Liang Wu
rdfs:label	Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (en) Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (nl)
skos:prefLabel	Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (en) Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (nl)
name	Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (en) Aminobromination of olefins with TsNH2and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (nl)
author	wds:Q57614691-AC389DD4-A4BE-4952-A7F1-0E1FC03EB52E
author	Guan-Wu Wang
title	wds:Q57614691-A0C15688-BEDA-42C2-AC14-2156974ECD25
title	Aminobromination of olefins with TsNH(2) and NBS as the nitrogen and bromine sources mediated by hypervalent iodine in a ball mill (en)
page(s)	wds:Q57614691-BC9DB7A5-E2F4-44A1-93DD-77DF14106A76
page(s)	548-553
instance of	wds:Q57614691-640B27EC-B518-4CC7-8D4F-879DA0E2CCAF
instance of	scholarly article
main subject	wds:Q57614691-0A84FD86-A9F9-410F-B151-E2E1DF023CA0 wds:Q57614691-6F173708-2411-4CF0-896F-C1D12C6B3B85 wds:Q57614691-7220672B-EABF-4328-A1F5-3DC5E57EA59A
main subject	iodine bromine iodine
PubMed ID	wds:Q57614691-C0658668-AEC9-45A9-B1EE-7D27BBDADB5A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18219426
PubMed ID	18219426
published in	wds:Q57614691-E2FC2CFF-0D32-44B7-858B-3900B6473CD9
published in	Organic and Biomolecular Chemistry
issue	wds:Q57614691-4570CCCA-49AF-4D88-8252-2A7166BA2F8E
volume	wds:Q57614691-356F112A-BDD4-448F-BB1B-D446765D220A
issue	3
volume	6
DOI	wds:Q57614691-C0D16F64-631B-4C0D-97E7-092F852F3932
DOI	http://dx.doi.org/10.1039/B717333D
DOI	10.1039/B717333D
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57614691
is cites work of	Mechanochemical organic synthesis. Iron-catalyzed asymmetric haloamination reactions Solvent-free bromination reactions with sodium bromide and oxone promoted by mechanical milling Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization Asymmetric iodoamination of chalcones and 4-aryl-4-oxobutenoates catalyzed by a complex based on scandium(III) and a N,N'-dioxide ligand. Efficient ZnBr2-catalyzed reactions of allylic alcohols with indoles, sulfamides and anilines under high-speed vibration milling conditions Aminohalogenation of Electron-Deficient Olefins Promoted by Hypervalent Iodine Compounds
is cites work of	wds:Q57614621-649F0DDA-1DCF-4D8F-A49A-DEA9C87A2FB0 wds:Q36600200-2B1237B0-E18C-4EF3-9740-17ED275B6E86 wds:Q57614551-CE7E2982-16AA-40DF-BE1E-16067291A9EF wds:Q38105451-D6BA56B4-D1D9-4E57-B270-09EE8D5A8D99 wds:Q45376627-05B5772C-1C0D-422D-B2CB-6F58F251218D wds:Q50506241-F4B754C8-A4D3-44AF-B6E6-90D2C2DAB2A3 wds:Q57614694-92737484-EF77-46F0-9907-8C1625CFC892

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