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Redox-Active Esters in Fe-Catalyzed C–C Coupling
[Image: see text] Cross-couplings of alkyl halides and organometallic species based on single electron transfer using Ni and Fe catalyst systems have been studied extensively, and separately, for decades. Here we demonstrate the first couplings of redox-active esters (both isolated and derived in si...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016806/ https://www.ncbi.nlm.nih.gov/pubmed/27548696 http://dx.doi.org/10.1021/jacs.6b07172 |
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author | Toriyama, Fumihiko Cornella, Josep Wimmer, Laurin Chen, Tie-Gen Dixon, Darryl D. Creech, Gardner Baran, Phil S. |
author_facet | Toriyama, Fumihiko Cornella, Josep Wimmer, Laurin Chen, Tie-Gen Dixon, Darryl D. Creech, Gardner Baran, Phil S. |
author_sort | Toriyama, Fumihiko |
collection | PubMed |
description | [Image: see text] Cross-couplings of alkyl halides and organometallic species based on single electron transfer using Ni and Fe catalyst systems have been studied extensively, and separately, for decades. Here we demonstrate the first couplings of redox-active esters (both isolated and derived in situ from carboxylic acids) with organozinc and organomagnesium species using an Fe-based catalyst system originally developed for alkyl halides. This work is placed in context by showing a direct comparison with a Ni catalyst for >40 examples spanning a range of primary, secondary, and tertiary substrates. This new C–C coupling is scalable and sustainable, and it exhibits a number of clear advantages in several cases over its Ni-based counterpart. |
format | Online Article Text |
id | pubmed-5016806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50168062016-09-13 Redox-Active Esters in Fe-Catalyzed C–C Coupling Toriyama, Fumihiko Cornella, Josep Wimmer, Laurin Chen, Tie-Gen Dixon, Darryl D. Creech, Gardner Baran, Phil S. J Am Chem Soc [Image: see text] Cross-couplings of alkyl halides and organometallic species based on single electron transfer using Ni and Fe catalyst systems have been studied extensively, and separately, for decades. Here we demonstrate the first couplings of redox-active esters (both isolated and derived in situ from carboxylic acids) with organozinc and organomagnesium species using an Fe-based catalyst system originally developed for alkyl halides. This work is placed in context by showing a direct comparison with a Ni catalyst for >40 examples spanning a range of primary, secondary, and tertiary substrates. This new C–C coupling is scalable and sustainable, and it exhibits a number of clear advantages in several cases over its Ni-based counterpart. American Chemical Society 2016-08-22 2016-09-07 /pmc/articles/PMC5016806/ /pubmed/27548696 http://dx.doi.org/10.1021/jacs.6b07172 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 | Toriyama, Fumihiko Cornella, Josep Wimmer, Laurin Chen, Tie-Gen Dixon, Darryl D. Creech, Gardner Baran, Phil S. Redox-Active Esters in Fe-Catalyzed C–C Coupling |
title | Redox-Active
Esters in Fe-Catalyzed C–C Coupling |
title_full | Redox-Active
Esters in Fe-Catalyzed C–C Coupling |
title_fullStr | Redox-Active
Esters in Fe-Catalyzed C–C Coupling |
title_full_unstemmed | Redox-Active
Esters in Fe-Catalyzed C–C Coupling |
title_short | Redox-Active
Esters in Fe-Catalyzed C–C Coupling |
title_sort | redox-active
esters in fe-catalyzed c–c coupling |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016806/ https://www.ncbi.nlm.nih.gov/pubmed/27548696 http://dx.doi.org/10.1021/jacs.6b07172 |
work_keys_str_mv | AT toriyamafumihiko redoxactiveestersinfecatalyzedcccoupling AT cornellajosep redoxactiveestersinfecatalyzedcccoupling AT wimmerlaurin redoxactiveestersinfecatalyzedcccoupling AT chentiegen redoxactiveestersinfecatalyzedcccoupling AT dixondarryld redoxactiveestersinfecatalyzedcccoupling AT creechgardner redoxactiveestersinfecatalyzedcccoupling AT baranphils redoxactiveestersinfecatalyzedcccoupling |