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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...

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Detalles Bibliográficos
Autores principales: Joyce, Leo A., Nawrat, Christopher C., Sherer, Edward C., Biba, Mirlinda, Brunskill, Andrew, Martin, Gary E., Cohen, Ryan D., Davies, Ian W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
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.
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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
title_full Beyond optical rotation: what's left is not always right in total synthesis
title_fullStr Beyond optical rotation: what's left is not always right in total synthesis
title_full_unstemmed Beyond optical rotation: what's left is not always right in total synthesis
title_short Beyond optical rotation: what's left is not always right in total synthesis
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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