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The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation
Planar chiral [2.2]paracyclophanes are resolved through the direct C–H arylation of enantiopure oxazolines, providing a convenient route to ligands and chiral materials. Preliminary results show that hydrolysis followed by decarboxylative phosphorylation leads to enantiopure [2.2]paracyclophane deri...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984818/ https://www.ncbi.nlm.nih.gov/pubmed/35424822 http://dx.doi.org/10.1039/d2ra01075e |
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author | Tewari, Shashank Mungalpara, Maulik N. Patel, Suraj Rowlands, Gareth J. |
author_facet | Tewari, Shashank Mungalpara, Maulik N. Patel, Suraj Rowlands, Gareth J. |
author_sort | Tewari, Shashank |
collection | PubMed |
description | Planar chiral [2.2]paracyclophanes are resolved through the direct C–H arylation of enantiopure oxazolines, providing a convenient route to ligands and chiral materials. Preliminary results show that hydrolysis followed by decarboxylative phosphorylation leads to enantiopure [2.2]paracyclophane derivatives that are otherwise challenging to prepare. |
format | Online Article Text |
id | pubmed-8984818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89848182022-04-13 The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation Tewari, Shashank Mungalpara, Maulik N. Patel, Suraj Rowlands, Gareth J. RSC Adv Chemistry Planar chiral [2.2]paracyclophanes are resolved through the direct C–H arylation of enantiopure oxazolines, providing a convenient route to ligands and chiral materials. Preliminary results show that hydrolysis followed by decarboxylative phosphorylation leads to enantiopure [2.2]paracyclophane derivatives that are otherwise challenging to prepare. The Royal Society of Chemistry 2022-03-17 /pmc/articles/PMC8984818/ /pubmed/35424822 http://dx.doi.org/10.1039/d2ra01075e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Tewari, Shashank Mungalpara, Maulik N. Patel, Suraj Rowlands, Gareth J. The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation |
title | The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation |
title_full | The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation |
title_fullStr | The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation |
title_full_unstemmed | The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation |
title_short | The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation |
title_sort | concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by c–h activation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984818/ https://www.ncbi.nlm.nih.gov/pubmed/35424822 http://dx.doi.org/10.1039/d2ra01075e |
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