About: Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions

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About: Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2000 (uk) im September 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 2000 (ast) scientific article published on 01 September 2000 (en)
publication date	wds:Q74316163-614AA957-087C-4AB7-B3BC-9302E3711FE5
publication date	2000-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q74316163-C8AC1277-7E76-4EBE-A4BA-25F5246436E6
language of work or name	English
author name string	wds:Q74316163-9F90A2F7-FC12-432B-A1EE-59CCF3A56841 wds:Q74316163-D86DF75A-3265-4305-B1BC-60FB2E5AC352
author name string	Hammerschmidt F Hanbauer M
rdfs:label	Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (en) Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (nl)
skos:prefLabel	Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (en) Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (nl)
name	Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (en) Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (nl)
title	wds:Q74316163-4E19EC5C-0BC4-47DF-B23F-D25993DFDF5D
title	Transformation of arylmethylamines into alpha-aminophosphonic acids via metalated phosphoramidates: rearrangement of partly configurationally stable N-phosphorylated alpha-aminocarbanions (en)
page(s)	wds:Q74316163-FF2C046F-2363-4F31-BFEA-BE46E1DBC8E8
page(s)	6121-6131
instance of	wds:Q74316163-10B65E0E-041E-4798-9AC8-54483E55EDA3
instance of	scholarly article
PubMed ID	wds:Q74316163-BA2D9F4C-186C-450A-8A8C-75E9C3AD6026
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10987948
PubMed ID	10987948
published in	wds:Q74316163-22A2E998-7B93-409F-B2CD-6C2CA4A3BD31
published in	Journal of Organic Chemistry
issue	wds:Q74316163-23955914-74E7-4C4E-84E4-7467CD78D453
volume	wds:Q74316163-2A92C558-549D-4757-B4A4-772482BB3F90
issue	19
volume	65
DOI	wds:Q74316163-C70BB594-446A-49F4-9D3D-5EB5BF05449B
DOI	http://dx.doi.org/10.1021/JO000585F
DOI	10.1021/JO000585F
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74316163
is cites work of	Targeting effector memory T cells with a selective peptide inhibitor of Kv1.3 channels for therapy of autoimmune diseases An Overview of Stereoselective Synthesis of α-Aminophosphonic Acids and Derivatives Asymmetric hydrophosphylation of chiral N-phosphonyl imines provides an efficient approach to chiral α-amino phosphonates α,β-Aziridinylphosphonates by lithium amide-induced phosphonyl migration from nitrogen to carbon in terminal aziridines Enantiodifferentiation of aminophosphonic and aminophosphinic acids with α- and β-cyclodextrins Enantioselective Borodeuteride Reduction of Aldimines Catalyzed by Cobalt Complexes: Preparation of Optically Active Deuterated Primary Amines An effective route to fluorine containing asymmetric alpha-aminophosphonates using chiral Bronsted acid catalyst. On the rearrangement of N-aryl-N-Boc-phosphoramidates to N-Boc-protected o-aminoarylphosphonates. Two Scaffolds from Two Flips: (α,β)/(β,γ) CH2/NH "Met-Im" Analogues of dTTP
is cites work of	wds:Q62631632-B7D6D13D-2E37-4603-875C-64AABD7314A9 wds:Q79079692-7C7DB4EA-E353-4D73-B153-3F491AF9BFD9 wds:Q47111013-2E91219F-7B06-4F65-8CAB-B83B7AC6AEB0 wds:Q34146575-D476AB6D-1A9A-4EDF-A810-8BEC87CE5BAA wds:Q36355109-1A5108B9-DAB6-4258-A6A9-2C5165D4F32A wds:Q28303760-82667D72-6E3A-49FF-BDA3-C2F87735FC7D wds:Q34312301-B9B66EA3-3839-43D2-A5CC-6941E5620C65 wds:Q34181879-C109F259-F946-4762-9522-6E7C36A80B44 wds:Q46432787-B98F34B2-05D0-43CD-AC59-CCBFFEF95EEF

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