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Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition

[Image: see text] Herein we report an oxyboration reaction with activated substrates that employs B–O σ bond additions to C–C π bonds to form borylated isoxazoles, which are potential building blocks for drug discovery. Although this reaction can be effectively catalyzed by gold, it is the first exa...

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Autores principales: Tu, Kim N., Hirner, Joshua J., Blum, Suzanne A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763986/
https://www.ncbi.nlm.nih.gov/pubmed/26771389
http://dx.doi.org/10.1021/acs.orglett.5b03530
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author Tu, Kim N.
Hirner, Joshua J.
Blum, Suzanne A.
author_facet Tu, Kim N.
Hirner, Joshua J.
Blum, Suzanne A.
author_sort Tu, Kim N.
collection PubMed
description [Image: see text] Herein we report an oxyboration reaction with activated substrates that employs B–O σ bond additions to C–C π bonds to form borylated isoxazoles, which are potential building blocks for drug discovery. Although this reaction can be effectively catalyzed by gold, it is the first example of uncatalyzed oxyboration of C–C π bonds by B–O σ bonds—and only the second example that is catalyzed. This oxyboration reaction is tolerant of groups incompatible with alternative lithiation/borylation and palladium-catalyzed C–H activation/borylation technologies for the synthesis of borylated isoxazoles.
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spelling pubmed-47639862017-01-15 Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition Tu, Kim N. Hirner, Joshua J. Blum, Suzanne A. Org Lett [Image: see text] Herein we report an oxyboration reaction with activated substrates that employs B–O σ bond additions to C–C π bonds to form borylated isoxazoles, which are potential building blocks for drug discovery. Although this reaction can be effectively catalyzed by gold, it is the first example of uncatalyzed oxyboration of C–C π bonds by B–O σ bonds—and only the second example that is catalyzed. This oxyboration reaction is tolerant of groups incompatible with alternative lithiation/borylation and palladium-catalyzed C–H activation/borylation technologies for the synthesis of borylated isoxazoles. American Chemical Society 2016-01-15 2016-02-05 /pmc/articles/PMC4763986/ /pubmed/26771389 http://dx.doi.org/10.1021/acs.orglett.5b03530 Text en Copyright © 2016 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 Tu, Kim N.
Hirner, Joshua J.
Blum, Suzanne A.
Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
title Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
title_full Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
title_fullStr Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
title_full_unstemmed Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
title_short Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
title_sort oxyboration with and without a catalyst: borylated isoxazoles via b–o σ-bond addition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763986/
https://www.ncbi.nlm.nih.gov/pubmed/26771389
http://dx.doi.org/10.1021/acs.orglett.5b03530
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