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Hydroxyl-Directed Stereoselective Diboration of Alkenes
[Image: see text] An alkoxide-catalyzed directed diboration of alkenyl alcohols is described. This reaction occurs in a stereoselective fashion and is demonstrated with cyclic and acyclic homoallylic and bishomoallylic alcohol substrates. After oxidation, the reaction generates 1,2-diols such that t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091278/ https://www.ncbi.nlm.nih.gov/pubmed/24941137 http://dx.doi.org/10.1021/ja504228p |
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author | Blaisdell, Thomas P. Caya, Thomas C. Zhang, Liang Sanz-Marco, Amparo Morken, James P. |
author_facet | Blaisdell, Thomas P. Caya, Thomas C. Zhang, Liang Sanz-Marco, Amparo Morken, James P. |
author_sort | Blaisdell, Thomas P. |
collection | PubMed |
description | [Image: see text] An alkoxide-catalyzed directed diboration of alkenyl alcohols is described. This reaction occurs in a stereoselective fashion and is demonstrated with cyclic and acyclic homoallylic and bishomoallylic alcohol substrates. After oxidation, the reaction generates 1,2-diols such that the process represents a method for the stereoselective directed dihydroxylation of alkenes. |
format | Online Article Text |
id | pubmed-4091278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40912782015-06-18 Hydroxyl-Directed Stereoselective Diboration of Alkenes Blaisdell, Thomas P. Caya, Thomas C. Zhang, Liang Sanz-Marco, Amparo Morken, James P. J Am Chem Soc [Image: see text] An alkoxide-catalyzed directed diboration of alkenyl alcohols is described. This reaction occurs in a stereoselective fashion and is demonstrated with cyclic and acyclic homoallylic and bishomoallylic alcohol substrates. After oxidation, the reaction generates 1,2-diols such that the process represents a method for the stereoselective directed dihydroxylation of alkenes. American Chemical Society 2014-06-18 2014-07-02 /pmc/articles/PMC4091278/ /pubmed/24941137 http://dx.doi.org/10.1021/ja504228p Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Blaisdell, Thomas P. Caya, Thomas C. Zhang, Liang Sanz-Marco, Amparo Morken, James P. Hydroxyl-Directed Stereoselective Diboration of Alkenes |
title | Hydroxyl-Directed
Stereoselective Diboration of Alkenes |
title_full | Hydroxyl-Directed
Stereoselective Diboration of Alkenes |
title_fullStr | Hydroxyl-Directed
Stereoselective Diboration of Alkenes |
title_full_unstemmed | Hydroxyl-Directed
Stereoselective Diboration of Alkenes |
title_short | Hydroxyl-Directed
Stereoselective Diboration of Alkenes |
title_sort | hydroxyl-directed
stereoselective diboration of alkenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091278/ https://www.ncbi.nlm.nih.gov/pubmed/24941137 http://dx.doi.org/10.1021/ja504228p |
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