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Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling

[Image: see text] Despite their importance, the synthesis of alkylated heterocycles from the cross-coupling of Lewis basic nitrogen heteroaryl halides with alkyl halides remains a challenge. We report here a general solution to this challenge enabled by a new collection of ligands based around 2-pyr...

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Autores principales: Hansen, Eric C., Li, Changfeng, Yang, Sihang, Pedro, Dylan, Weix, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539790/
https://www.ncbi.nlm.nih.gov/pubmed/28682073
http://dx.doi.org/10.1021/acs.joc.7b01334
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author Hansen, Eric C.
Li, Changfeng
Yang, Sihang
Pedro, Dylan
Weix, Daniel J.
author_facet Hansen, Eric C.
Li, Changfeng
Yang, Sihang
Pedro, Dylan
Weix, Daniel J.
author_sort Hansen, Eric C.
collection PubMed
description [Image: see text] Despite their importance, the synthesis of alkylated heterocycles from the cross-coupling of Lewis basic nitrogen heteroaryl halides with alkyl halides remains a challenge. We report here a general solution to this challenge enabled by a new collection of ligands based around 2-pyridyl-N-cyanocarboxamidine and 2-pyridylcarboxamidine cores. Both primary and secondary alkyl halides can be coupled with 2-, 3-, and 4-pyridyl halides as well as other more complex heterocycles in generally good yields (41 examples, 69% ave yield).
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spelling pubmed-55397902018-07-06 Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling Hansen, Eric C. Li, Changfeng Yang, Sihang Pedro, Dylan Weix, Daniel J. J Org Chem [Image: see text] Despite their importance, the synthesis of alkylated heterocycles from the cross-coupling of Lewis basic nitrogen heteroaryl halides with alkyl halides remains a challenge. We report here a general solution to this challenge enabled by a new collection of ligands based around 2-pyridyl-N-cyanocarboxamidine and 2-pyridylcarboxamidine cores. Both primary and secondary alkyl halides can be coupled with 2-, 3-, and 4-pyridyl halides as well as other more complex heterocycles in generally good yields (41 examples, 69% ave yield). American Chemical Society 2017-07-06 2017-07-21 /pmc/articles/PMC5539790/ /pubmed/28682073 http://dx.doi.org/10.1021/acs.joc.7b01334 Text en Copyright © 2017 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 Hansen, Eric C.
Li, Changfeng
Yang, Sihang
Pedro, Dylan
Weix, Daniel J.
Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling
title Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling
title_full Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling
title_fullStr Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling
title_full_unstemmed Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling
title_short Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling
title_sort coupling of challenging heteroaryl halides with alkyl halides via nickel-catalyzed cross-electrophile coupling
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539790/
https://www.ncbi.nlm.nih.gov/pubmed/28682073
http://dx.doi.org/10.1021/acs.joc.7b01334
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