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Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis

We report herein a novel approach involving optical resolution of (±)-1,16-dihydroxytetraphenylene (DHTP) by chiral gold(iii) complexation. This method features several key advantages, i.e., recyclability of chiral resolution reagents, feasibility of scaling up to gram quantities, and operational si...

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Autores principales: Guo, Jia, Xiong, Wen-Bin, Ma, Hao-Ran, Fan, Luoyi, Zhou, You-Yun, Wong, Henry N. C., Cui, Jian-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020179/
https://www.ncbi.nlm.nih.gov/pubmed/35656141
http://dx.doi.org/10.1039/d2sc00388k
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author Guo, Jia
Xiong, Wen-Bin
Ma, Hao-Ran
Fan, Luoyi
Zhou, You-Yun
Wong, Henry N. C.
Cui, Jian-Fang
author_facet Guo, Jia
Xiong, Wen-Bin
Ma, Hao-Ran
Fan, Luoyi
Zhou, You-Yun
Wong, Henry N. C.
Cui, Jian-Fang
author_sort Guo, Jia
collection PubMed
description We report herein a novel approach involving optical resolution of (±)-1,16-dihydroxytetraphenylene (DHTP) by chiral gold(iii) complexation. This method features several key advantages, i.e., recyclability of chiral resolution reagents, feasibility of scaling up to gram quantities, and operational simplicity. On the basis of this method, which led to optically pure DHTP, a library of 2,15-diaryl (S)-DHTPs and several (S)-DHTP-derived phosphoramidite ligands were synthesized. Finally, the superior performance of a (S)-DHTP phosphoramidite ligand was demonstrated by efficient iridium-catalyzed asymmetric allylic alkynylation reactions.
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spelling pubmed-90201792022-06-01 Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis Guo, Jia Xiong, Wen-Bin Ma, Hao-Ran Fan, Luoyi Zhou, You-Yun Wong, Henry N. C. Cui, Jian-Fang Chem Sci Chemistry We report herein a novel approach involving optical resolution of (±)-1,16-dihydroxytetraphenylene (DHTP) by chiral gold(iii) complexation. This method features several key advantages, i.e., recyclability of chiral resolution reagents, feasibility of scaling up to gram quantities, and operational simplicity. On the basis of this method, which led to optically pure DHTP, a library of 2,15-diaryl (S)-DHTPs and several (S)-DHTP-derived phosphoramidite ligands were synthesized. Finally, the superior performance of a (S)-DHTP phosphoramidite ligand was demonstrated by efficient iridium-catalyzed asymmetric allylic alkynylation reactions. The Royal Society of Chemistry 2022-03-24 /pmc/articles/PMC9020179/ /pubmed/35656141 http://dx.doi.org/10.1039/d2sc00388k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Guo, Jia
Xiong, Wen-Bin
Ma, Hao-Ran
Fan, Luoyi
Zhou, You-Yun
Wong, Henry N. C.
Cui, Jian-Fang
Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
title Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
title_full Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
title_fullStr Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
title_full_unstemmed Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
title_short Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
title_sort optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020179/
https://www.ncbi.nlm.nih.gov/pubmed/35656141
http://dx.doi.org/10.1039/d2sc00388k
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