Please use this identifier to cite or link to this item: doi:10.22028/D291-37845
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Title: The Addition of a Cyclopropyl Alkyne to an Asymmetrically-Substituted Disilene: A Mechanistic Study
Author(s): Henry, Andrew T.
Bourque, Jeremy L.
Vacirca, Isabell
Scheschkewitz, David
Baines, Kim M.
Language: English
Title: Organometallics
Volume: 38
Issue: 7
Pages: 1622–1626
Publisher/Platform: American Chemical Society
Year of Publication: 2019
Free key words: Group 14 compounds
Hydrocarbons
Phenyls
Silicon
Substituents
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: The addition of (2-ethynyl-3-methoxy-2-methylcyclopropyl)benzene to Tip2Si═SiTipPh, a disilene with an asymmetric substitution pattern, was investigated. The regiochemistry of the ring-opened products indicates a stepwise mechanism with a biradical intermediate. The results are consistent with those obtained in similar experiments with symmetrically substituted disilenes.
DOI of the first publication: 10.1021/acs.organomet.9b00054
URL of the first publication: https://pubs.acs.org/doi/10.1021/acs.organomet.9b00054
Link to this record: urn:nbn:de:bsz:291--ds-378458
hdl:20.500.11880/34221
http://dx.doi.org/10.22028/D291-37845
ISSN: 1520-6041
0276-7333
Date of registration: 7-Nov-2022
Description of the related object: Supporting Information
Related object: https://pubs.acs.org/doi/suppl/10.1021/acs.organomet.9b00054/suppl_file/om9b00054_si_001.pdf
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Chemie
Professorship: NT - Prof. Dr. David Scheschkewitz
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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