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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
Main Authors: Rodríguez, David, Mulero, Marlenne, Prieto, José A
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cited_by cdi_FETCH-LOGICAL-a381t-d06e0193662d17adea3120201c86f579aef92f2bb55a0fbc28b5e198ad40d2513
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container_end_page 5829
container_issue 15
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container_title Journal of organic chemistry
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creator Rodríguez, David
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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
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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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