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An Efficient Approach to Mechanically Planar Chiral Rotaxanes
[Image: see text] We describe the first method for production of mechanically planar chiral rotaxanes in excellent enantiopurity without the use of chiral separation techniques and, for the first time, unambiguously assign the absolute stereochemistry of the products. This proof-of-concept study, wh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977585/ https://www.ncbi.nlm.nih.gov/pubmed/24559064 http://dx.doi.org/10.1021/ja412715m |
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author | Bordoli, Robert J. Goldup, Stephen M. |
author_facet | Bordoli, Robert J. Goldup, Stephen M. |
author_sort | Bordoli, Robert J. |
collection | PubMed |
description | [Image: see text] We describe the first method for production of mechanically planar chiral rotaxanes in excellent enantiopurity without the use of chiral separation techniques and, for the first time, unambiguously assign the absolute stereochemistry of the products. This proof-of-concept study, which employs a chiral pool sugar as the source of asymmetry and a high-yielding active template reaction for mechanical bond formation, finally opens the door to detailed investigation of these challenging targets. |
format | Online Article Text |
id | pubmed-3977585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39775852014-04-07 An Efficient Approach to Mechanically Planar Chiral Rotaxanes Bordoli, Robert J. Goldup, Stephen M. J Am Chem Soc [Image: see text] We describe the first method for production of mechanically planar chiral rotaxanes in excellent enantiopurity without the use of chiral separation techniques and, for the first time, unambiguously assign the absolute stereochemistry of the products. This proof-of-concept study, which employs a chiral pool sugar as the source of asymmetry and a high-yielding active template reaction for mechanical bond formation, finally opens the door to detailed investigation of these challenging targets. American Chemical Society 2014-02-22 2014-04-02 /pmc/articles/PMC3977585/ /pubmed/24559064 http://dx.doi.org/10.1021/ja412715m Text en Copyright © 2014 American Chemical Society Terms of Use CC-BY (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) |
spellingShingle | Bordoli, Robert J. Goldup, Stephen M. An Efficient Approach to Mechanically Planar Chiral Rotaxanes |
title | An Efficient
Approach to Mechanically Planar Chiral
Rotaxanes |
title_full | An Efficient
Approach to Mechanically Planar Chiral
Rotaxanes |
title_fullStr | An Efficient
Approach to Mechanically Planar Chiral
Rotaxanes |
title_full_unstemmed | An Efficient
Approach to Mechanically Planar Chiral
Rotaxanes |
title_short | An Efficient
Approach to Mechanically Planar Chiral
Rotaxanes |
title_sort | efficient
approach to mechanically planar chiral
rotaxanes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977585/ https://www.ncbi.nlm.nih.gov/pubmed/24559064 http://dx.doi.org/10.1021/ja412715m |
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