Please use this identifier to cite or link to this item: doi:10.22028/D291-43365
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Title: Stereoselective Synthesis of Highly Substituted O-Heterocycles via Matteson Homologation: A Ring-Closing Metathesis Approach
Author(s): Kinsinger, Thorsten
Schäfer, Patrick
Kazmaier, Uli
Language: English
Title: Organic Letters
Volume: 25
Issue: 18
Pages: 3303-3307
Publisher/Platform: ACS
Year of Publication: 2023
Free key words: Alcohols
Anions
Chemical Synthesis
Metathesis
Organic Compounds
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Matteson homologations of chiral boronic esters with the aid of unsaturated nucleophiles are powerful for gaining access to a range of different O-heterocycles via subsequent ring-closing metatheses. Using this protocol, six- to eight-membered rings become available and almost any position of the ring can be substituted and/or functionalized.
DOI of the first publication: 10.1021/acs.orglett.3c01099
URL of the first publication: https://pubs.acs.org/doi/10.1021/acs.orglett.3c01099
Link to this record: urn:nbn:de:bsz:291--ds-433652
hdl:20.500.11880/38893
http://dx.doi.org/10.22028/D291-43365
ISSN: 1523-7052
1523-7060
Date of registration: 6-Nov-2024
Description of the related object: Supporting Information
Related object: https://ndownloader.figstatic.com/files/40335447
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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