Pd-catalyzed direct C2-acylation and C2,C7-diacylation of indoles: pyrimidine as an easily removable C–H directing group
Pyrimidine is successfully used as an easily removable C(sp 2 )–H directing group for the synthesis of 2-acyl indoles and 2,7-diacyl indoles through direct C–H functionalization using a Pd-catalyst from 1-(pyrimidin-2-yl)-1 H -indoles and aldehydes. Easy removal of the pyrimidine directing group usi...
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Veröffentlicht in: | RSC advances 2015-01, Vol.5 (36), p.28292-28298 |
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container_issue | 36 |
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container_title | RSC advances |
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creator | Kumar, Govindharaj Sekar, Govindasamy |
description | Pyrimidine is successfully used as an easily removable C(sp
2
)–H directing group for the synthesis of 2-acyl indoles and 2,7-diacyl indoles through direct C–H functionalization using a Pd-catalyst from 1-(pyrimidin-2-yl)-1
H
-indoles and aldehydes. Easy removal of the pyrimidine directing group using EtONa in DMSO provides C2-acyl indoles. |
doi_str_mv | 10.1039/C4RA15162C |
format | Article |
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)–H directing group for the synthesis of 2-acyl indoles and 2,7-diacyl indoles through direct C–H functionalization using a Pd-catalyst from 1-(pyrimidin-2-yl)-1
H
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)–H directing group for the synthesis of 2-acyl indoles and 2,7-diacyl indoles through direct C–H functionalization using a Pd-catalyst from 1-(pyrimidin-2-yl)-1
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2
)–H directing group for the synthesis of 2-acyl indoles and 2,7-diacyl indoles through direct C–H functionalization using a Pd-catalyst from 1-(pyrimidin-2-yl)-1
H
-indoles and aldehydes. Easy removal of the pyrimidine directing group using EtONa in DMSO provides C2-acyl indoles.</abstract><doi>10.1039/C4RA15162C</doi><tpages>7</tpages></addata></record> |
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ispartof | RSC advances, 2015-01, Vol.5 (36), p.28292-28298 |
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language | eng |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Aldehydes Indoles Palladium Pyrimidines Synthesis |
title | Pd-catalyzed direct C2-acylation and C2,C7-diacylation of indoles: pyrimidine as an easily removable C–H directing group |
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