About: 1-(-Acylamino)alkyltriarylphosphonium Salts with Weakened C-P⁺ Bond Strength-Synthetic Applications

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About: 1-(-Acylamino)alkyltriarylphosphonium Salts with Weakened C-P⁺ Bond Strength-Synthetic Applications Goto Sponge NotDistinct Permalink

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scientific article published on 25 September 2018

Attributes	Values
rdf:type	Item
description	наукова стаття, опублікована у вересні 2018 (uk) im September 2018 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 2018 (ast) scientific article published on 25 September 2018 (en)
publication date	wds:Q58692243-4937BDF0-87C4-4117-8C82-FBA4C1F47A22
publication date	2018-09-25 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58692243-56728750-722E-4FA3-8716-0934D4280753
language of work or name	English
cites work	wds:Q58692243-0E8BAA61-F76C-4532-BCD9-8EE21B938353 wds:Q58692243-3907BD94-AAE8-4401-98FB-90E4AAD63994 wds:Q58692243-3F67495E-56A7-4034-A6A6-26524B74246E wds:Q58692243-4F77C68F-CF03-4958-A377-913415B1CCD2 wds:Q58692243-576DD2CC-8C6F-4F58-BBE0-8175D8357F8B wds:Q58692243-5AA13772-E18F-457A-A1CD-B0DF3693A25C wds:Q58692243-69EF8DFE-1F06-4B97-954C-0B75365AD098 wds:Q58692243-8FEA8864-55B3-468B-B176-43ACAFBEDCDD wds:Q58692243-8FF831CB-95DC-403A-B545-05D9728945B3 wds:Q58692243-9698DDC4-CFE0-4445-9429-32BBE5C908A7 wds:Q58692243-9CBF196D-97EC-440F-9157-39FDB0957FCA wds:Q58692243-9E959A1E-545F-4225-AA3E-2367A4D440D7 wds:Q58692243-9ECF26D9-0148-4B1F-9671-8EF811669C3A wds:Q58692243-C935362B-D88F-4D04-A9D0-448611070E33
cites work	Alpha-amido sulfones as stable precursors of reactive N-acylimino derivatives Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) Cyclizations ofN-Acyliminium Ions A simple and efficient access to alpha-amino phosphonates from N-benzyloxycarbonylamino sulfones using indium(III) chloride. InBr3: a versatile catalyst for the different types of Friedel-Crafts reactions Solventless clay-promoted Friedel-Crafts reaction of indoles with alpha-amido sulfones: unexpected synthesis of 3-(1-arylsulfonylalkyl) indoles α-Amidoalkylating agents from N-acyl-α-amino acids: 1-(N-acylamino)alkyltriphenylphosphonium salts Properties and Synthetic Utility of N-Substituted Benzotriazoles Chiral Brønsted Acid-Catalyzed Enantioselective α-Amidoalkylation Reactions: A Joint Experimental and Predictive Study Enolizable Carbonyls and N,O-Acetals: A Rational Approach for Room-Temperature Lewis Superacid-Catalyzed Direct α-Amidoalkylation of Ketones and Aldehydes. The first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane Bi(OTf)3-Catalyzed Multicomponent α-Amidoalkylation Reactions 1-Imidoalkylphosphonium salts with modulated Cα-P+ bond strength: synthesis and application as new active α-imidoalkylating agents. 1-(N-acylamino)alkyl sulfones from N-acyl-α-amino acids or N-alkylamides
author name string	wds:Q58692243-4230390F-CAF6-4DFC-81B4-F5C3ABFBF393 wds:Q58692243-47FFC5B4-43D8-4856-84E9-BF59BEE045E1 wds:Q58692243-E1E96184-A7B3-4D05-AA35-8D56CF23270C
author name string	Karol Erfurt Anna Węgrzyk Justyna Kończewicz
rdfs:label	1-(-Acylamino)alkyltriarylphosphonium Salts with Weakened C-P⁺ Bond Strength-Synthetic Applications (en)
skos:prefLabel	1-(-Acylamino)alkyltriarylphosphonium Salts with Weakened C-P⁺ Bond Strength-Synthetic Applications (en)
name	1-(-Acylamino)alkyltriarylphosphonium Salts with Weakened C-P⁺ Bond Strength-Synthetic Applications (en)
author	wds:Q58692243-5F8313E9-D8DC-4F85-BE03-8E3B1E169B48 wds:Q58692243-ADDADC7A-B804-4677-A83E-73DE83C5CD1D
author	Jakub Adamek Krzysztof Walczak
title	wds:Q58692243-FA7DA5E2-8BF5-48D4-8C0E-A4C24D2DA0C5
title	1-(N-Acylamino)alkyltriarylphosphonium Salts with Weakened Cα-P⁺ Bond Strength-Synthetic Applications (en)
page(s)	wds:Q58692243-0188347D-2D18-457A-BC27-6F9444C09D0D
page(s)	2453
instance of	wds:Q58692243-3AB11933-0BAF-46C2-89FA-899038CB8B43
instance of	scholarly article
PubMed ID	wds:Q58692243-BBB396D1-3E32-4C35-BE8C-242871BC38B2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30257468
PubMed ID	30257468
published in	wds:Q58692243-DFA4C73C-832A-44A7-8FDD-66F0C2E1EB31
published in	Molecules
issue	wds:Q58692243-B810ADC9-EA92-4DA1-AB18-D4647DCD53F3
volume	wds:Q58692243-9DD679E1-F951-4BD4-9E86-4C3BE5B07FFC
issue	10
volume	23
DOI	wds:Q58692243-04C6D3E2-F755-4955-98CB-A3C436AB06EF
DOI	http://dx.doi.org/10.3390/MOLECULES23102453
DOI	10.3390/MOLECULES23102453
copyright license	wds:Q58692243-a37b25e3-a20e-4edb-9a22-772223522747
copyright status	wds:Q58692243-5bf71a69-608c-4078-8e54-39759b14e50d
copyright license	Creative Commons Attribution 4.0 International
copyright status	copyrighted
PMCID	wds:Q58692243-4F9D32C7-6710-4713-8A7F-3EFE9A9032D8
PMCID	6222910
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58692243
is cites work of	Michaelis-Arbuzov-Type Reaction of 1-Imidoalkyltriarylphosphonium Salts with Selected Phosphorus Nucleophiles
is cites work of	wds:Q90226051-63BA74C3-A65B-4CE8-A373-27C1CEA941BF

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