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General Method for Functionalized Polyaryl Synthesis via Aryne Intermediates
[Image: see text] A method for base-promoted arylation of arenes and heterocycles by aryl halides and aryl triflates is described. Additionally, in situ electrophilic trapping of ArLi intermediates generated in the reaction of benzyne with deprotonated arenes or heterocycles has been developed, prov...
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/PMC4227807/ https://www.ncbi.nlm.nih.gov/pubmed/24893069 http://dx.doi.org/10.1021/ja504886x |
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author | Truong, Thanh Mesgar, Milad Le, Ky Khac Anh Daugulis, Olafs |
author_facet | Truong, Thanh Mesgar, Milad Le, Ky Khac Anh Daugulis, Olafs |
author_sort | Truong, Thanh |
collection | PubMed |
description | [Image: see text] A method for base-promoted arylation of arenes and heterocycles by aryl halides and aryl triflates is described. Additionally, in situ electrophilic trapping of ArLi intermediates generated in the reaction of benzyne with deprotonated arenes or heterocycles has been developed, providing rapid and easy access to a wide range of highly functionalized polyaryls. Base-promoted arylation methodology complements transition-metal-catalyzed direct arylation and allows access to structures that are not easily accessible via other direct arylation methods. The reactions are highly functional-group tolerant, with alkene, ether, dimethylamino, trifluoromethyl, ester, cyano, halide, hydroxyl, and silyl functionalities compatible with reaction conditions. |
format | Online Article Text |
id | pubmed-4227807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42278072015-06-03 General Method for Functionalized Polyaryl Synthesis via Aryne Intermediates Truong, Thanh Mesgar, Milad Le, Ky Khac Anh Daugulis, Olafs J Am Chem Soc [Image: see text] A method for base-promoted arylation of arenes and heterocycles by aryl halides and aryl triflates is described. Additionally, in situ electrophilic trapping of ArLi intermediates generated in the reaction of benzyne with deprotonated arenes or heterocycles has been developed, providing rapid and easy access to a wide range of highly functionalized polyaryls. Base-promoted arylation methodology complements transition-metal-catalyzed direct arylation and allows access to structures that are not easily accessible via other direct arylation methods. The reactions are highly functional-group tolerant, with alkene, ether, dimethylamino, trifluoromethyl, ester, cyano, halide, hydroxyl, and silyl functionalities compatible with reaction conditions. American Chemical Society 2014-06-03 2014-06-18 /pmc/articles/PMC4227807/ /pubmed/24893069 http://dx.doi.org/10.1021/ja504886x Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Truong, Thanh Mesgar, Milad Le, Ky Khac Anh Daugulis, Olafs General Method for Functionalized Polyaryl Synthesis via Aryne Intermediates |
title | General
Method for Functionalized Polyaryl Synthesis
via Aryne Intermediates |
title_full | General
Method for Functionalized Polyaryl Synthesis
via Aryne Intermediates |
title_fullStr | General
Method for Functionalized Polyaryl Synthesis
via Aryne Intermediates |
title_full_unstemmed | General
Method for Functionalized Polyaryl Synthesis
via Aryne Intermediates |
title_short | General
Method for Functionalized Polyaryl Synthesis
via Aryne Intermediates |
title_sort | general
method for functionalized polyaryl synthesis
via aryne intermediates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227807/ https://www.ncbi.nlm.nih.gov/pubmed/24893069 http://dx.doi.org/10.1021/ja504886x |
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