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ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds

The development of metal-free organic reactions is one of the hotspots in the synthesis of cyclic compounds. ROTf (alkyl trifluoromethanesulfonates), due to their good electrophilicity, are powerful alkylating reagents at heteroatoms such as nitrogen, oxygen, sulfur and phosphorus to induce an elect...

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Detalles Bibliográficos
Autores principales: Zou, Song, Wang, Sheng, Xi, Chanjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281944/
https://www.ncbi.nlm.nih.gov/pubmed/30564422
http://dx.doi.org/10.1098/rsos.181389
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author Zou, Song
Wang, Sheng
Xi, Chanjuan
author_facet Zou, Song
Wang, Sheng
Xi, Chanjuan
author_sort Zou, Song
collection PubMed
description The development of metal-free organic reactions is one of the hotspots in the synthesis of cyclic compounds. ROTf (alkyl trifluoromethanesulfonates), due to their good electrophilicity, are powerful alkylating reagents at heteroatoms such as nitrogen, oxygen, sulfur and phosphorus to induce an electrophilic centre for carbon–carbon or carbon–heteroatom bond formation. Inspired by this chemistry, a variety of research concentrating on heterocycles synthesis has been carried out. In this review, we mainly summarize the ROTf-induced annulation of heteroatom reagents such as nitriles, carbodiimides, azobenzenes, isothiocyanates, aldehydes, isocyanates and phosphaalkene with themselves or alkynes to afford cyclic compounds.
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spelling pubmed-62819442018-12-18 ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds Zou, Song Wang, Sheng Xi, Chanjuan R Soc Open Sci Chemistry The development of metal-free organic reactions is one of the hotspots in the synthesis of cyclic compounds. ROTf (alkyl trifluoromethanesulfonates), due to their good electrophilicity, are powerful alkylating reagents at heteroatoms such as nitrogen, oxygen, sulfur and phosphorus to induce an electrophilic centre for carbon–carbon or carbon–heteroatom bond formation. Inspired by this chemistry, a variety of research concentrating on heterocycles synthesis has been carried out. In this review, we mainly summarize the ROTf-induced annulation of heteroatom reagents such as nitriles, carbodiimides, azobenzenes, isothiocyanates, aldehydes, isocyanates and phosphaalkene with themselves or alkynes to afford cyclic compounds. The Royal Society 2018-11-07 /pmc/articles/PMC6281944/ /pubmed/30564422 http://dx.doi.org/10.1098/rsos.181389 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Zou, Song
Wang, Sheng
Xi, Chanjuan
ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
title ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
title_full ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
title_fullStr ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
title_full_unstemmed ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
title_short ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
title_sort rotf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281944/
https://www.ncbi.nlm.nih.gov/pubmed/30564422
http://dx.doi.org/10.1098/rsos.181389
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AT xichanjuan rotfinducedannulationofheteroatomreagentsandunsaturatedsubstratesleadingtocycliccompounds