New Blatter-type radicals from a bench-stable carbene

Blatter’s radicals are highly valuable stable organic free radicals, comprising a heterocyclic ring system functionalized with a heteroaryl or alkyl group at the C-3 position. Here, the authors report a synthetic strategy to obtain Blatter’s radical substituted with an amine and amide group.

Bibliographic Details
Main Authors:	Jacob A. Grant, Zhou Lu, David E. Tucker, Bryony M. Hockin, Dmitry S. Yufit, Mark A. Fox, Ritu Kataky, Victor Chechik, AnnMarie C. O’Donoghue
Format:	Article
Language:	English
Published:	Nature Publishing Group 2017-05-01
Series:	Nature Communications
Online Access:	https://doi.org/10.1038/ncomms15088

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spelling	doaj-9fde64cbd7a442cfb61319e4c9fe420e2021-05-11T07:34:57ZengNature Publishing GroupNature Communications2041-17232017-05-01811610.1038/ncomms15088New Blatter-type radicals from a bench-stable carbeneJacob A. Grant0Zhou Lu1David E. Tucker2Bryony M. Hockin3Dmitry S. Yufit4Mark A. Fox5Ritu Kataky6Victor Chechik7AnnMarie C. O’Donoghue8Department of Chemistry, Durham UniversityDepartment of Chemistry, University of YorkDepartment of Chemistry, Durham UniversityDepartment of Chemistry, Durham UniversityDepartment of Chemistry, Durham UniversityDepartment of Chemistry, Durham UniversityDepartment of Chemistry, Durham UniversityDepartment of Chemistry, University of YorkDepartment of Chemistry, Durham UniversityBlatter’s radicals are highly valuable stable organic free radicals, comprising a heterocyclic ring system functionalized with a heteroaryl or alkyl group at the C-3 position. Here, the authors report a synthetic strategy to obtain Blatter’s radical substituted with an amine and amide group.https://doi.org/10.1038/ncomms15088
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Jacob A. Grant Zhou Lu David E. Tucker Bryony M. Hockin Dmitry S. Yufit Mark A. Fox Ritu Kataky Victor Chechik AnnMarie C. O’Donoghue
spellingShingle	Jacob A. Grant Zhou Lu David E. Tucker Bryony M. Hockin Dmitry S. Yufit Mark A. Fox Ritu Kataky Victor Chechik AnnMarie C. O’Donoghue New Blatter-type radicals from a bench-stable carbene Nature Communications
author_facet	Jacob A. Grant Zhou Lu David E. Tucker Bryony M. Hockin Dmitry S. Yufit Mark A. Fox Ritu Kataky Victor Chechik AnnMarie C. O’Donoghue
author_sort	Jacob A. Grant
title	New Blatter-type radicals from a bench-stable carbene
title_short	New Blatter-type radicals from a bench-stable carbene
title_full	New Blatter-type radicals from a bench-stable carbene
title_fullStr	New Blatter-type radicals from a bench-stable carbene
title_full_unstemmed	New Blatter-type radicals from a bench-stable carbene
title_sort	new blatter-type radicals from a bench-stable carbene
publisher	Nature Publishing Group
series	Nature Communications
issn	2041-1723
publishDate	2017-05-01
description	Blatter’s radicals are highly valuable stable organic free radicals, comprising a heterocyclic ring system functionalized with a heteroaryl or alkyl group at the C-3 position. Here, the authors report a synthetic strategy to obtain Blatter’s radical substituted with an amine and amide group.
url	https://doi.org/10.1038/ncomms15088
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New Blatter-type radicals from a bench-stable carbene

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