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Reinvestigation of a Catalytic, Enantioselective Alkene Dibromination and Chlorohydroxylation
[Image: see text] Attempts to reproduce eight, putative, enantioselective dibromination and chlorohydroxylation reactions from oft-cited literature studies are described. The reactions were performed with full fidelity to the original report wherever possible. Analysis of the enantiomeric compositio...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672746/ https://www.ncbi.nlm.nih.gov/pubmed/26566099 http://dx.doi.org/10.1021/acs.orglett.5b02650 |
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author | Denmark, Scott E. Carson, Nessa |
author_facet | Denmark, Scott E. Carson, Nessa |
author_sort | Denmark, Scott E. |
collection | PubMed |
description | [Image: see text] Attempts to reproduce eight, putative, enantioselective dibromination and chlorohydroxylation reactions from oft-cited literature studies are described. The reactions were performed with full fidelity to the original report wherever possible. Analysis of the enantiomeric composition was performed by chiral stationary phase HPLC or SFC (CSP-HPLC or CSP-SFC), as opposed to the original report, which used chiral shift reagent NMR spectroscopy. After careful study, the reported levels of enantioselectivity were found to be incorrect. Possible explanations for the false positive results are discussed. |
format | Online Article Text |
id | pubmed-4672746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-46727462015-12-23 Reinvestigation of a Catalytic, Enantioselective Alkene Dibromination and Chlorohydroxylation Denmark, Scott E. Carson, Nessa Org Lett [Image: see text] Attempts to reproduce eight, putative, enantioselective dibromination and chlorohydroxylation reactions from oft-cited literature studies are described. The reactions were performed with full fidelity to the original report wherever possible. Analysis of the enantiomeric composition was performed by chiral stationary phase HPLC or SFC (CSP-HPLC or CSP-SFC), as opposed to the original report, which used chiral shift reagent NMR spectroscopy. After careful study, the reported levels of enantioselectivity were found to be incorrect. Possible explanations for the false positive results are discussed. American Chemical Society 2015-11-13 2015-12-04 /pmc/articles/PMC4672746/ /pubmed/26566099 http://dx.doi.org/10.1021/acs.orglett.5b02650 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Denmark, Scott E. Carson, Nessa Reinvestigation of a Catalytic, Enantioselective Alkene Dibromination and Chlorohydroxylation |
title | Reinvestigation of a Catalytic, Enantioselective Alkene
Dibromination and Chlorohydroxylation |
title_full | Reinvestigation of a Catalytic, Enantioselective Alkene
Dibromination and Chlorohydroxylation |
title_fullStr | Reinvestigation of a Catalytic, Enantioselective Alkene
Dibromination and Chlorohydroxylation |
title_full_unstemmed | Reinvestigation of a Catalytic, Enantioselective Alkene
Dibromination and Chlorohydroxylation |
title_short | Reinvestigation of a Catalytic, Enantioselective Alkene
Dibromination and Chlorohydroxylation |
title_sort | reinvestigation of a catalytic, enantioselective alkene
dibromination and chlorohydroxylation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672746/ https://www.ncbi.nlm.nih.gov/pubmed/26566099 http://dx.doi.org/10.1021/acs.orglett.5b02650 |
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