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Beyond optical rotation: what's left is not always right in total synthesis
This work describes the application of vibrational (VCD) and electronic (ECD) circular dichroism spectroscopy to solve the longstanding debate around the absolute configuration of (+)-frondosin B (1). The absolute configuration of (+)-1 could confidently be assigned as (R) using these spectroscopic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868320/ https://www.ncbi.nlm.nih.gov/pubmed/29629112 http://dx.doi.org/10.1039/c7sc04249c |
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author | Joyce, Leo A. Nawrat, Christopher C. Sherer, Edward C. Biba, Mirlinda Brunskill, Andrew Martin, Gary E. Cohen, Ryan D. Davies, Ian W. |
author_facet | Joyce, Leo A. Nawrat, Christopher C. Sherer, Edward C. Biba, Mirlinda Brunskill, Andrew Martin, Gary E. Cohen, Ryan D. Davies, Ian W. |
author_sort | Joyce, Leo A. |
collection | PubMed |
description | This work describes the application of vibrational (VCD) and electronic (ECD) circular dichroism spectroscopy to solve the longstanding debate around the absolute configuration of (+)-frondosin B (1). The absolute configuration of (+)-1 could confidently be assigned as (R) using these spectroscopic techniques. The discrepancy in the optical rotation (OR) values obtained in previous studies can be attributed to an undetected minor impurity (ca. 7%) that arose unexpectedly in a key step late in the synthesis. Additionally, the conditions used in the final step of the previous reports for demethylation to form the natural product proceeded with significant loss of enantiopurity. The large OR measured for the impurity at its observed level, when compared to the small rotation for the less enantiopure natural product 1, led to a measured OR value for the synthetic material that had the opposite sign of the natural product. |
format | Online Article Text |
id | pubmed-5868320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-58683202018-04-06 Beyond optical rotation: what's left is not always right in total synthesis Joyce, Leo A. Nawrat, Christopher C. Sherer, Edward C. Biba, Mirlinda Brunskill, Andrew Martin, Gary E. Cohen, Ryan D. Davies, Ian W. Chem Sci Chemistry This work describes the application of vibrational (VCD) and electronic (ECD) circular dichroism spectroscopy to solve the longstanding debate around the absolute configuration of (+)-frondosin B (1). The absolute configuration of (+)-1 could confidently be assigned as (R) using these spectroscopic techniques. The discrepancy in the optical rotation (OR) values obtained in previous studies can be attributed to an undetected minor impurity (ca. 7%) that arose unexpectedly in a key step late in the synthesis. Additionally, the conditions used in the final step of the previous reports for demethylation to form the natural product proceeded with significant loss of enantiopurity. The large OR measured for the impurity at its observed level, when compared to the small rotation for the less enantiopure natural product 1, led to a measured OR value for the synthetic material that had the opposite sign of the natural product. Royal Society of Chemistry 2017-10-30 /pmc/articles/PMC5868320/ /pubmed/29629112 http://dx.doi.org/10.1039/c7sc04249c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Joyce, Leo A. Nawrat, Christopher C. Sherer, Edward C. Biba, Mirlinda Brunskill, Andrew Martin, Gary E. Cohen, Ryan D. Davies, Ian W. Beyond optical rotation: what's left is not always right in total synthesis |
title | Beyond optical rotation: what's left is not always right in total synthesis
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title_full | Beyond optical rotation: what's left is not always right in total synthesis
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title_fullStr | Beyond optical rotation: what's left is not always right in total synthesis
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title_full_unstemmed | Beyond optical rotation: what's left is not always right in total synthesis
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title_short | Beyond optical rotation: what's left is not always right in total synthesis
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title_sort | beyond optical rotation: what's left is not always right in total synthesis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868320/ https://www.ncbi.nlm.nih.gov/pubmed/29629112 http://dx.doi.org/10.1039/c7sc04249c |
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