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Investigations into the C-deuteriation of silyl enol ethers derived from aryl alkyl ketones
Results are reported on the regioselective C‐deuteriation of a series of silyl enol ethers derived from aryl alkyl ketones using deuterium (D2) gas as the deuterium source and palladium‐on‐barium sulfate as the mediator. These results highlight the numerous reaction pathways and different product ty...
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Published in: | Journal of labelled compounds & radiopharmaceuticals 2006-08, Vol.49 (9), p.757-771 |
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container_end_page | 771 |
container_issue | 9 |
container_start_page | 757 |
container_title | Journal of labelled compounds & radiopharmaceuticals |
container_volume | 49 |
creator | Buksha, Svitlana Coumbarides, Gregory S. Dingjan, Marco Eames, Jason Suggate, Michael J. Weerasooriya, Neluka |
description | Results are reported on the regioselective C‐deuteriation of a series of silyl enol ethers derived from aryl alkyl ketones using deuterium (D2) gas as the deuterium source and palladium‐on‐barium sulfate as the mediator. These results highlight the numerous reaction pathways and different product types available from simple deuteriation of substituted enol precursors. Copyright © 2006 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jlcr.1088 |
format | article |
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These results highlight the numerous reaction pathways and different product types available from simple deuteriation of substituted enol precursors. 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These results highlight the numerous reaction pathways and different product types available from simple deuteriation of substituted enol precursors. Copyright © 2006 John Wiley & Sons, Ltd.</description><subject>alkyl aryl ketones</subject><subject>Chemistry</subject><subject>Condensed benzenic and aromatic compounds</subject><subject>deuteriation</subject><subject>Exact sciences and technology</subject><subject>hydrogenation</subject><subject>Organic chemistry</subject><subject>palladium</subject><subject>Preparations and properties</subject><subject>reduction</subject><subject>silyl enol ethers and silyl ethers</subject><issn>0362-4803</issn><issn>1099-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpFkMFOwzAQRC0EEqVw4A984Ri6zqaOc0QR0FYVSAjUAwfLsR1wmyaVHQr9e1yK4LK70ptZjYaQSwbXDCAdLRvt4yXEERkwKIqEYZYdkwEgT5NMAJ6SsxCWAJFl2YC8TtutDb17U73r2kBd23e0f7e0TIz96K13P4B2NQ2u2TXUtl0cUeEDNRFvraG179ZU-UhVs4pzZfuuteGcnNSqCfbidw_Jy93tczlJ5o_30_JmnriUo0gqbYBp5GBibFMwobNaC-BCY50qsKKyJtdmzCvkudBgsWCpMQqY4lWqAYfk6vB3o4JWTe1Vq12QG-_WMZRkAsZCIIu60UH36Rq7--cg99XJfXVyX52czcun_REdycHhQm-__hzKryTPMR_LxcO95LjgkxmCRPwGz4dz-w</recordid><startdate>200608</startdate><enddate>200608</enddate><creator>Buksha, Svitlana</creator><creator>Coumbarides, Gregory S.</creator><creator>Dingjan, Marco</creator><creator>Eames, Jason</creator><creator>Suggate, Michael J.</creator><creator>Weerasooriya, Neluka</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope></search><sort><creationdate>200608</creationdate><title>Investigations into the C-deuteriation of silyl enol ethers derived from aryl alkyl ketones</title><author>Buksha, Svitlana ; Coumbarides, Gregory S. ; Dingjan, Marco ; Eames, Jason ; Suggate, Michael J. ; Weerasooriya, Neluka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2638-bcd01c360d088d918c4fc8068c3f2a0e8bed7cd56b3678c0e3912dda01a6b2c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>alkyl aryl ketones</topic><topic>Chemistry</topic><topic>Condensed benzenic and aromatic compounds</topic><topic>deuteriation</topic><topic>Exact sciences and technology</topic><topic>hydrogenation</topic><topic>Organic chemistry</topic><topic>palladium</topic><topic>Preparations and properties</topic><topic>reduction</topic><topic>silyl enol ethers and silyl ethers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buksha, Svitlana</creatorcontrib><creatorcontrib>Coumbarides, Gregory S.</creatorcontrib><creatorcontrib>Dingjan, Marco</creatorcontrib><creatorcontrib>Eames, Jason</creatorcontrib><creatorcontrib>Suggate, Michael J.</creatorcontrib><creatorcontrib>Weerasooriya, Neluka</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buksha, Svitlana</au><au>Coumbarides, Gregory S.</au><au>Dingjan, Marco</au><au>Eames, Jason</au><au>Suggate, Michael J.</au><au>Weerasooriya, Neluka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigations into the C-deuteriation of silyl enol ethers derived from aryl alkyl ketones</atitle><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle><addtitle>J Label Compd Radiopharm</addtitle><date>2006-08</date><risdate>2006</risdate><volume>49</volume><issue>9</issue><spage>757</spage><epage>771</epage><pages>757-771</pages><issn>0362-4803</issn><eissn>1099-1344</eissn><abstract>Results are reported on the regioselective C‐deuteriation of a series of silyl enol ethers derived from aryl alkyl ketones using deuterium (D2) gas as the deuterium source and palladium‐on‐barium sulfate as the mediator. 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language | eng |
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subjects | alkyl aryl ketones Chemistry Condensed benzenic and aromatic compounds deuteriation Exact sciences and technology hydrogenation Organic chemistry palladium Preparations and properties reduction silyl enol ethers and silyl ethers |
title | Investigations into the C-deuteriation of silyl enol ethers derived from aryl alkyl ketones |
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