Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor

Determining results of asymmetric reactions can take long periods of time and consume large amounts of organic solvents during work-up and analysis. Here, the authors report a bifunctional organic probe that can bind to chiral hydroxyacids, and provide yield, enantiomeric excess and absolute configu...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Keith W. Bentley, Daysi Proano, Christian Wolf
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2016
Materias:
Q
Acceso en línea:https://doaj.org/article/e77f8baa04984dda8c81a509c2b86eab
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:e77f8baa04984dda8c81a509c2b86eab
record_format dspace
spelling oai:doaj.org-article:e77f8baa04984dda8c81a509c2b86eab2021-12-02T16:57:29ZChirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor10.1038/ncomms125392041-1723https://doaj.org/article/e77f8baa04984dda8c81a509c2b86eab2016-08-01T00:00:00Zhttps://doi.org/10.1038/ncomms12539https://doaj.org/toc/2041-1723Determining results of asymmetric reactions can take long periods of time and consume large amounts of organic solvents during work-up and analysis. Here, the authors report a bifunctional organic probe that can bind to chiral hydroxyacids, and provide yield, enantiomeric excess and absolute configuration even with crude mixtures.Keith W. BentleyDaysi ProanoChristian WolfNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-8 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Keith W. Bentley
Daysi Proano
Christian Wolf
Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor
description Determining results of asymmetric reactions can take long periods of time and consume large amounts of organic solvents during work-up and analysis. Here, the authors report a bifunctional organic probe that can bind to chiral hydroxyacids, and provide yield, enantiomeric excess and absolute configuration even with crude mixtures.
format article
author Keith W. Bentley
Daysi Proano
Christian Wolf
author_facet Keith W. Bentley
Daysi Proano
Christian Wolf
author_sort Keith W. Bentley
title Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor
title_short Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor
title_full Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor
title_fullStr Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor
title_full_unstemmed Chirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptor
title_sort chirality imprinting and direct asymmetric reaction screening using a stereodynamic brønsted/lewis acid receptor
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/e77f8baa04984dda8c81a509c2b86eab
work_keys_str_mv AT keithwbentley chiralityimprintinganddirectasymmetricreactionscreeningusingastereodynamicbrønstedlewisacidreceptor
AT daysiproano chiralityimprintinganddirectasymmetricreactionscreeningusingastereodynamicbrønstedlewisacidreceptor
AT christianwolf chiralityimprintinganddirectasymmetricreactionscreeningusingastereodynamicbrønstedlewisacidreceptor
_version_ 1718382596436525056