About: C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 18 April 2011

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2011 (uk) article scientifique publié en 2011 (fr) im April 2011 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 18 April 2011 (en) artículu científicu espublizáu n'abril de 2011 (ast)
publication date	wds:Q56985487-3EFB319E-6A2D-4E0F-9AE7-B7BE6012A602
publication date	2011-04-18 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56985487-3733E06B-E182-4B9B-8482-45CFF0734930
language of work or name	English
cites work	wds:Q56985487-045FCF05-86BE-49DE-9958-0388ABC0DB40 wds:Q56985487-106133A5-085F-4341-BD28-D285358B2B84 wds:Q56985487-1E012CD5-2EE0-491D-A78B-C835C93D31E1 wds:Q56985487-2D5F7909-8CA1-41F4-BCD2-0EC3053E1A82 wds:Q56985487-32D06065-7CAF-4907-85CC-97D8F8D69937 wds:Q56985487-348CE061-E3E7-469B-8B8A-C8F8AEF7F705 wds:Q56985487-34C12179-5524-4A82-B055-61859D852539 wds:Q56985487-39E1BAB5-6318-4EF9-9191-DB68A72043B9 wds:Q56985487-3B0EC68D-B99B-4A3A-889D-47E99E525768 wds:Q56985487-43037753-EDF1-4614-9AAD-4720F78FC79D wds:Q56985487-453A91EE-96BE-48FE-BC7E-02B2D9BC9F19 wds:Q56985487-48C65724-5BBA-4A54-ACFE-7ED72F104C85 wds:Q56985487-57A214DE-F399-4FAC-A3D9-424149A4D532 wds:Q56985487-59AC3AC7-58AE-4288-AA5B-69C032ACF1CB wds:Q56985487-5EF30CEC-12F1-41AB-9AF8-E2C5A0C89F6F wds:Q56985487-7C969D53-C381-4CE5-9E09-561B121D20F5 wds:Q56985487-7E7F0C07-E74F-450F-86ED-5333EB640BD9 wds:Q56985487-81C64585-44DB-4A98-B508-E6C1A8D6DE95 wds:Q56985487-9817B572-1425-4320-BAD3-57942F7DE21C wds:Q56985487-A684E29A-8664-452E-A1EF-244FC0ADFDD6 wds:Q56985487-A89DFE12-C2A7-400B-B162-A0EB60A7E4A3 wds:Q56985487-B04E1063-2654-4503-8BDB-77053B8976C8 wds:Q56985487-B1C4FB68-DF6A-4805-BAD9-18BB369EF9A9 wds:Q56985487-B320DCFE-A791-4CC8-AC1B-365940205659 wds:Q56985487-B513FBDE-CC86-40A5-A3DA-F72355FD2B01 wds:Q56985487-B5D85D3A-ADAF-44F8-8025-9CBF792B676E wds:Q56985487-CB1EA45C-CC08-4D04-9023-988975B40256 wds:Q56985487-CF3D0512-13EE-49A2-A63C-1D37803E2C96 wds:Q56985487-D1F22157-6AD5-463A-A0FE-B3329B55E094 wds:Q56985487-DAFF1927-294B-45BB-9F82-2493F668ECE9 wds:Q56985487-DDACB35D-97F6-40E0-A9E3-6AF05B82F7DC wds:Q56985487-DE687702-D258-4D05-9F9E-FF83FC45D134 wds:Q56985487-E53F7D0D-CA1B-4696-ABF3-DD3FBFF672FD wds:Q56985487-F2AD35B4-AD91-486F-979E-589744E23CCA
cites work	A cyclohexyl-1,2-diamine-derived bis(binaphthyl) macrocycle: enhanced sensitivity and enantioselectivity in the fluorescent recognition of mandelic acid Electronic structure calculations on workstation computers: The program system turbomole An enantioselective NMR shift reagent for cationic aromatics cclib: A library for package-independent computational chemistry algorithms Geometries and properties of excited states in the gas phase and in solution: theory and application of a time-dependent density functional theory polarizable continuum model. NMR determination of enantiomeric purity Fluorescence of organic molecules in chiral recognition A facile circular dichroism protocol for rapid determination of enantiomeric excess and concentration of chiral primary amines Colorimetric enantiodiscrimination of alpha-amino acids in protic media Time-Resolved IR-Thermographic Detection and Screening of Enantioselectivity in Catalytic Reactions. Semiempirical hybrid density functional with perturbative second-order correlation Trianglamines--readily prepared, conformationally flexible inclusion-forming chiral hexamines. Determination of absolute configuration using ab initio calculation of optical rotation Determination of absolute configuration using concerted ab Initio DFT calculations of electronic circular dichroism and optical rotation: bicyclo[3.3.1]nonane diones Facile optical resolution of tert-butanethiosulfinate by molecular complexation with (R)-BINOL and study of chiral discrimination of the diastereomeric complexes Polarizable Continuum Model (PCM) Calculations of Solvent Effects on Optical Rotations of Chiral Molecules Double-hybrid density functional theory for excited electronic states of molecules Calculation of electronic circular dichroism spectra with time-dependent double-hybrid density functional theory Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols Using enantioselective indicator displacement assays to determine the enantiomeric excess of alpha-amino acids Thiourea and isothiocyanate--two useful chromophores for stereochemical studies. A comparison of experiment and computation. Optically active macrocyclic hexaazapyridinophanes decorated at the periphery: synthesis and applications in the NMR enantiodiscrimination of carboxylic acids Enantioselective recognition of carboxylates: a receptor derived from alpha-aminoxy acids functions as a chiral shift reagent for carboxylic acids New pincer-like receptor derived from trans-cyclopentane-1,2-diamine as a chiral shift reagent for carboxylic acids An azamacrocyclic receptor as efficient polytopic chiral solvating agent for carboxylic acids Highly sensitive chiral shift reagent bearing two zinc porphyrins. Enantioselective recognition of a chiral quaternary ammonium ion by C3 symmetric cyclic hexapeptides. Chiral Molecular Receptors Based on Trans-Cyclohexane-1,2-diamine Enantiodiscrimination by NMR spectroscopy. Enantiodifferentiation of alpha-hydroxyalkanephosphonic acids in 31P NMR with application of alpha-cyclodextrin as chiral discriminating agent Cycloalkane-1,2-diamine derivatives as chiral solvating agents. Study of the structural variables controlling the NMR enantiodiscrimination of chiral carboxylic acids Tuning the chiral cavity of macrocyclic receptor for chiral recognition and discrimination. Novel chiral derivatizing isothiocyanate-based agent for the enantiomeric excess determination of amines. Stereoselective synthesis of ring C-hexasubstituted trianglamines
author name string	wds:Q56985487-03359BE5-D49A-4E45-A5A2-F66B66489313 wds:Q56985487-713CFFBA-62D3-409F-8629-A2B3DC81A984
author name string	Diego Savoia Stefano Grilli
rdfs:label	C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (en) C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (nl)
skos:prefLabel	C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (en) C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (nl)
name	C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (en) C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (nl)
author	wds:Q56985487-252C6E30-3D59-4CAC-9E5A-5557F5B6399A wds:Q56985487-63095297-84D0-4CB0-B68A-FAA6B2E39589 wds:Q56985487-640EA53F-DADE-4D1D-92BE-76160169ED89
author	Marcin Kwit Jacek Gawroński Andrea Gualandi
title	wds:Q56985487-803E1779-C461-4126-B351-CC38F7F24FBE
title	C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids (en)
page(s)	wds:Q56985487-DB3FD1FF-3B92-49DC-A560-2E90CBD40BF6
page(s)	4234-4241
instance of	wds:Q56985487-302269C3-BB88-41E4-8CA1-6B3072F7FC39

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 171 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software