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Functionalized spirolactones by photoinduced dearomatization of biaryl compounds

The idea of using biaryl structures to generate synthetic building blocks such as spirolactones is attractive because biaryl structures are abundant in biomass waste streams. However, the inertness of aromatic rings of biaryls makes it challenging to transform them into functionalized structures. In...

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Detalles Bibliográficos
Autores principales: Li, Hongji, Subbotina, Elena, Bunrit, Anon, Wang, Feng, Samec, Joseph S. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438148/
https://www.ncbi.nlm.nih.gov/pubmed/30996963
http://dx.doi.org/10.1039/c8sc05476b
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author Li, Hongji
Subbotina, Elena
Bunrit, Anon
Wang, Feng
Samec, Joseph S. M.
author_facet Li, Hongji
Subbotina, Elena
Bunrit, Anon
Wang, Feng
Samec, Joseph S. M.
author_sort Li, Hongji
collection PubMed
description The idea of using biaryl structures to generate synthetic building blocks such as spirolactones is attractive because biaryl structures are abundant in biomass waste streams. However, the inertness of aromatic rings of biaryls makes it challenging to transform them into functionalized structures. In this work, we developed photoinduced dearomatization of nonphenolic biaryl compounds to generate spirolactones. We demonstrate that dearomatization can be performed via either aerobic photocatalysis or anaerobic photooxidation to tolerate specific synthetic conditions. In both pathways, dearomatization is induced by electrophilic attack of the carboxyl radical. The resulting spirodiene radical is captured by either oxygen or water in aerobic and anaerobic systems, respectively, to generate the spirodienone. These methods represent novel routes to synthesize spirolactones from the biaryl motif.
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spelling pubmed-64381482019-04-17 Functionalized spirolactones by photoinduced dearomatization of biaryl compounds Li, Hongji Subbotina, Elena Bunrit, Anon Wang, Feng Samec, Joseph S. M. Chem Sci Chemistry The idea of using biaryl structures to generate synthetic building blocks such as spirolactones is attractive because biaryl structures are abundant in biomass waste streams. However, the inertness of aromatic rings of biaryls makes it challenging to transform them into functionalized structures. In this work, we developed photoinduced dearomatization of nonphenolic biaryl compounds to generate spirolactones. We demonstrate that dearomatization can be performed via either aerobic photocatalysis or anaerobic photooxidation to tolerate specific synthetic conditions. In both pathways, dearomatization is induced by electrophilic attack of the carboxyl radical. The resulting spirodiene radical is captured by either oxygen or water in aerobic and anaerobic systems, respectively, to generate the spirodienone. These methods represent novel routes to synthesize spirolactones from the biaryl motif. Royal Society of Chemistry 2019-02-19 /pmc/articles/PMC6438148/ /pubmed/30996963 http://dx.doi.org/10.1039/c8sc05476b Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Li, Hongji
Subbotina, Elena
Bunrit, Anon
Wang, Feng
Samec, Joseph S. M.
Functionalized spirolactones by photoinduced dearomatization of biaryl compounds
title Functionalized spirolactones by photoinduced dearomatization of biaryl compounds
title_full Functionalized spirolactones by photoinduced dearomatization of biaryl compounds
title_fullStr Functionalized spirolactones by photoinduced dearomatization of biaryl compounds
title_full_unstemmed Functionalized spirolactones by photoinduced dearomatization of biaryl compounds
title_short Functionalized spirolactones by photoinduced dearomatization of biaryl compounds
title_sort functionalized spirolactones by photoinduced dearomatization of biaryl compounds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438148/
https://www.ncbi.nlm.nih.gov/pubmed/30996963
http://dx.doi.org/10.1039/c8sc05476b
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