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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...

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Autores principales: Denmark, Scott E., Carson, Nessa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
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.
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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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