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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...

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Autores principales: Truong, Thanh, Mesgar, Milad, Le, Ky Khac Anh, Daugulis, Olafs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
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.
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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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