Cargando…

α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones

We present a metal-free method for α-acetoxyarone synthesis by self-intermolecular oxidative coupling of aryl ketones using I(2)−tert-butyl hydroperoxide (TBHP). Under the optimum conditions, various aryl ketones gave the corresponding products in moderate to excellent yields. A series of control ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Tan, Liquan, Chen, Cui, Liu, Weibing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480364/
https://www.ncbi.nlm.nih.gov/pubmed/28684987
http://dx.doi.org/10.3762/bjoc.13.107
_version_ 1783245283358932992
author Tan, Liquan
Chen, Cui
Liu, Weibing
author_facet Tan, Liquan
Chen, Cui
Liu, Weibing
author_sort Tan, Liquan
collection PubMed
description We present a metal-free method for α-acetoxyarone synthesis by self-intermolecular oxidative coupling of aryl ketones using I(2)−tert-butyl hydroperoxide (TBHP). Under the optimum conditions, various aryl ketones gave the corresponding products in moderate to excellent yields. A series of control experiments were performed; the results suggest the involvement of radical pathways. Multiple radical intermediates were generated in situ and the overall process involved several different reactions, which proceeded self-sequentially in a single reactor. A labeling experiment using (18)O-labeled H(2)O confirmed that the oxygen in the product was derived from TBHP, not from H(2)O in the TBHP solvent.
format Online
Article
Text
id pubmed-5480364
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-54803642017-07-06 α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones Tan, Liquan Chen, Cui Liu, Weibing Beilstein J Org Chem Letter We present a metal-free method for α-acetoxyarone synthesis by self-intermolecular oxidative coupling of aryl ketones using I(2)−tert-butyl hydroperoxide (TBHP). Under the optimum conditions, various aryl ketones gave the corresponding products in moderate to excellent yields. A series of control experiments were performed; the results suggest the involvement of radical pathways. Multiple radical intermediates were generated in situ and the overall process involved several different reactions, which proceeded self-sequentially in a single reactor. A labeling experiment using (18)O-labeled H(2)O confirmed that the oxygen in the product was derived from TBHP, not from H(2)O in the TBHP solvent. Beilstein-Institut 2017-06-06 /pmc/articles/PMC5480364/ /pubmed/28684987 http://dx.doi.org/10.3762/bjoc.13.107 Text en Copyright © 2017, Tan et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Tan, Liquan
Chen, Cui
Liu, Weibing
α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
title α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
title_full α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
title_fullStr α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
title_full_unstemmed α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
title_short α-Acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
title_sort α-acetoxyarone synthesis via iodine-catalyzed and tert-butyl hydroperoxide-mediateded self-intermolecular oxidative coupling of aryl ketones
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480364/
https://www.ncbi.nlm.nih.gov/pubmed/28684987
http://dx.doi.org/10.3762/bjoc.13.107
work_keys_str_mv AT tanliquan aacetoxyaronesynthesisviaiodinecatalyzedandtertbutylhydroperoxidemediatededselfintermolecularoxidativecouplingofarylketones
AT chencui aacetoxyaronesynthesisviaiodinecatalyzedandtertbutylhydroperoxidemediatededselfintermolecularoxidativecouplingofarylketones
AT liuweibing aacetoxyaronesynthesisviaiodinecatalyzedandtertbutylhydroperoxidemediatededselfintermolecularoxidativecouplingofarylketones