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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...

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Autores principales: Toriyama, Fumihiko, Cornella, Josep, Wimmer, Laurin, Chen, Tie-Gen, Dixon, Darryl D., Creech, Gardner, Baran, Phil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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
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AT chentiegen redoxactiveestersinfecatalyzedcccoupling
AT dixondarryld redoxactiveestersinfecatalyzedcccoupling
AT creechgardner redoxactiveestersinfecatalyzedcccoupling
AT baranphils redoxactiveestersinfecatalyzedcccoupling