Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes.
The pendant methylsulfanyl group of aldehyde 1 provides chelation stabilization (see 3), thus allowing direct hydroacylation of functionalized electron-poor alkenes 2 in good yields under mild conditions. Electron-deficient alkynes can also be used as substrates. R = ester, arnide, imide, sulfone; d...
Main Authors: | , , |
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Format: | Journal article |
Language: | English |
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2004
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author | Willis, M McNally, S Beswick, P |
author_facet | Willis, M McNally, S Beswick, P |
author_sort | Willis, M |
collection | OXFORD |
description | The pendant methylsulfanyl group of aldehyde 1 provides chelation stabilization (see 3), thus allowing direct hydroacylation of functionalized electron-poor alkenes 2 in good yields under mild conditions. Electron-deficient alkynes can also be used as substrates. R = ester, arnide, imide, sulfone; dppe = 1,2-bis(diphenylphosphanyl)ethane. |
first_indexed | 2024-03-07T01:56:02Z |
format | Journal article |
id | oxford-uuid:9bbf6f46-5745-4b89-a1df-b016ba4243cc |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T01:56:02Z |
publishDate | 2004 |
record_format | dspace |
spelling | oxford-uuid:9bbf6f46-5745-4b89-a1df-b016ba4243cc2022-03-27T00:30:57ZChelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9bbf6f46-5745-4b89-a1df-b016ba4243ccEnglishSymplectic Elements at Oxford2004Willis, MMcNally, SBeswick, PThe pendant methylsulfanyl group of aldehyde 1 provides chelation stabilization (see 3), thus allowing direct hydroacylation of functionalized electron-poor alkenes 2 in good yields under mild conditions. Electron-deficient alkynes can also be used as substrates. R = ester, arnide, imide, sulfone; dppe = 1,2-bis(diphenylphosphanyl)ethane. |
spellingShingle | Willis, M McNally, S Beswick, P Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. |
title | Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. |
title_full | Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. |
title_fullStr | Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. |
title_full_unstemmed | Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. |
title_short | Chelation-controlled intermolecular hydroacylation: direct addition of alkyl aldehydes to functionalized alkenes. |
title_sort | chelation controlled intermolecular hydroacylation direct addition of alkyl aldehydes to functionalized alkenes |
work_keys_str_mv | AT willism chelationcontrolledintermolecularhydroacylationdirectadditionofalkylaldehydestofunctionalizedalkenes AT mcnallys chelationcontrolledintermolecularhydroacylationdirectadditionofalkylaldehydestofunctionalizedalkenes AT beswickp chelationcontrolledintermolecularhydroacylationdirectadditionofalkylaldehydestofunctionalizedalkenes |