Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones
An intramolecular dehydrogenative C–H activation enabled an efficient synthesis of an uracil-annulated β-carbolinone ring system. The reaction is simple, efficient and high yielding (85–92%).
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2015
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578345/ |
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pubmed-45783452015-09-30 Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones Mondal, Biplab Hazra, Somjit Panda, Tarun K Roy, Brindaban Full Research Paper An intramolecular dehydrogenative C–H activation enabled an efficient synthesis of an uracil-annulated β-carbolinone ring system. The reaction is simple, efficient and high yielding (85–92%). Beilstein-Institut 2015-08-04 /pmc/articles/PMC4578345/ /pubmed/26425190 http://dx.doi.org/10.3762/bjoc.11.146 Text en Copyright © 2015, Mondal et al; licensee Beilstein-Institut. http://www.beilstein-journals.org/bjoc This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 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: (http://www.beilstein-journals.org/bjoc) |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Mondal, Biplab Hazra, Somjit Panda, Tarun K Roy, Brindaban |
spellingShingle |
Mondal, Biplab Hazra, Somjit Panda, Tarun K Roy, Brindaban Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones |
author_facet |
Mondal, Biplab Hazra, Somjit Panda, Tarun K Roy, Brindaban |
author_sort |
Mondal, Biplab |
title |
Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones |
title_short |
Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones |
title_full |
Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones |
title_fullStr |
Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones |
title_full_unstemmed |
Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones |
title_sort |
pd(oac)2-catalyzed dehydrogenative c–h activation: an expedient synthesis of uracil-annulated β-carbolinones |
description |
An intramolecular dehydrogenative C–H activation enabled an efficient synthesis of an uracil-annulated β-carbolinone ring system. The reaction is simple, efficient and high yielding (85–92%). |
publisher |
Beilstein-Institut |
publishDate |
2015 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578345/ |
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1613478162450087936 |