Please use this identifier to cite or link to this item: doi:10.22028/D291-43387
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Title: Application of Vinyl Nucleophiles in Matteson Homologations
Author(s): Kinsinger, Thorsten
Kazmaier, Uli
Language: English
Title: Organic Letters
Volume: 24
Issue: 20
Pages: 3599-3603
Publisher/Platform: ACS
Year of Publication: 2022
Free key words: Anions
Chemical Reactions
Organic Compounds
Reagents
Vinyl
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: The Matteson homologation with vinyl nucleophiles was found to be a versatile tool for the synthesis of highly substituted and functionalized allyl boronic esters. High yields and stereoselectivities are obtained with sterically demanding alkyl boronic esters and/or Grignard reagents. With the application of such vinyl Matteson homologations, the polyketide fragment of lagunamide B is synthesized.
DOI of the first publication: 10.1021/acs.orglett.2c01119
URL of the first publication: https://pubs.acs.org/doi/10.1021/acs.orglett.2c01119
Link to this record: urn:nbn:de:bsz:291--ds-433878
hdl:20.500.11880/38907
http://dx.doi.org/10.22028/D291-43387
ISSN: 1523-7052
1523-7060
Date of registration: 7-Nov-2024
Description of the related object: Supporting Information
Related object: https://pubs.acs.org/doi/suppl/10.1021/acs.orglett.2c01119/suppl_file/ol2c01119_si_001.pdf
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Chemie
Professorship: NT - Prof. Dr. Uli Kazmaier
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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