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Highly Regioselective Copper-Catalyzed cis- and trans-1-Propenyl Grignard Cleavage of Hindered Epoxides. Application in Propionate Synthesis
Hindered protected and unprotected epoxy alcohols were regioselectively cleaved using copper-catalyzed cis- and trans-1-propenylmagnesium bromide. The reaction exhibited good yield and excellent regioselectivity in systems where organocuprates and organoalanes failed. The cis Grignard reagent displa...
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Published in: | Journal of organic chemistry 2006-07, Vol.71 (15), p.5826-5829 |
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cites | cdi_FETCH-LOGICAL-a381t-d06e0193662d17adea3120201c86f579aef92f2bb55a0fbc28b5e198ad40d2513 |
container_end_page | 5829 |
container_issue | 15 |
container_start_page | 5826 |
container_title | Journal of organic chemistry |
container_volume | 71 |
creator | Rodríguez, David Mulero, Marlenne Prieto, José A |
description | Hindered protected and unprotected epoxy alcohols were regioselectively cleaved using copper-catalyzed cis- and trans-1-propenylmagnesium bromide. The reaction exhibited good yield and excellent regioselectivity in systems where organocuprates and organoalanes failed. The cis Grignard reagent displayed no double-bond isomerization, whereas the trans isomer showed partial trans-to-cis equilibration, which was minimized by controlling the reagent formation conditions. The reaction was shown to be highly useful for the elaboration of the C10−C15 Streptovaricin D ansa chain fragment. |
doi_str_mv | 10.1021/jo060833t |
format | article |
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Application in Propionate Synthesis</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>2006-07-21</date><risdate>2006</risdate><volume>71</volume><issue>15</issue><spage>5826</spage><epage>5829</epage><pages>5826-5829</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><coden>JOCEAH</coden><abstract>Hindered protected and unprotected epoxy alcohols were regioselectively cleaved using copper-catalyzed cis- and trans-1-propenylmagnesium bromide. The reaction exhibited good yield and excellent regioselectivity in systems where organocuprates and organoalanes failed. The cis Grignard reagent displayed no double-bond isomerization, whereas the trans isomer showed partial trans-to-cis equilibration, which was minimized by controlling the reagent formation conditions. The reaction was shown to be highly useful for the elaboration of the C10−C15 Streptovaricin D ansa chain fragment.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16839177</pmid><doi>10.1021/jo060833t</doi><tpages>4</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Alkenes - chemical synthesis Alkenes - chemistry Alkynes - chemistry Catalysis Chemistry Copper - chemistry Epoxy Compounds - chemistry Epoxy Compounds - metabolism Exact sciences and technology Molecular Structure Organic chemistry Propionates - chemical synthesis Propionates - chemistry Stereoisomerism |
title | Highly Regioselective Copper-Catalyzed cis- and trans-1-Propenyl Grignard Cleavage of Hindered Epoxides. Application in Propionate Synthesis |
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