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Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines

Intermolecular hydroaminoalkylation reactions of symmetrical and unsymmetrical alkynes with tertiary amines take place in the presence of catalytic amounts of TiBn(4), Ph(3)C[B(C(6)F(5))(4)], and a sterically demanding aminopyridinato ligand precursor. The resulting products, synthetically and pharm...

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Detalles Bibliográficos
Autores principales: Kaper, Tobias, Geik, Dennis, Fornfeist, Felix, Schmidtmann, Marc, Doye, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303398/
https://www.ncbi.nlm.nih.gov/pubmed/34936144
http://dx.doi.org/10.1002/chem.202103931
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author Kaper, Tobias
Geik, Dennis
Fornfeist, Felix
Schmidtmann, Marc
Doye, Sven
author_facet Kaper, Tobias
Geik, Dennis
Fornfeist, Felix
Schmidtmann, Marc
Doye, Sven
author_sort Kaper, Tobias
collection PubMed
description Intermolecular hydroaminoalkylation reactions of symmetrical and unsymmetrical alkynes with tertiary amines take place in the presence of catalytic amounts of TiBn(4), Ph(3)C[B(C(6)F(5))(4)], and a sterically demanding aminopyridinato ligand precursor. The resulting products, synthetically and pharmaceutically useful tertiary β,γ‐disubstituted allylic amines, are formed in convincing yields and with excellent stereoselectivity. Particularly promising for future applications is the fact that even the industrial side product trimethylamine can be used as a substrate.
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spelling pubmed-93033982022-07-22 Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines Kaper, Tobias Geik, Dennis Fornfeist, Felix Schmidtmann, Marc Doye, Sven Chemistry Research Articles Intermolecular hydroaminoalkylation reactions of symmetrical and unsymmetrical alkynes with tertiary amines take place in the presence of catalytic amounts of TiBn(4), Ph(3)C[B(C(6)F(5))(4)], and a sterically demanding aminopyridinato ligand precursor. The resulting products, synthetically and pharmaceutically useful tertiary β,γ‐disubstituted allylic amines, are formed in convincing yields and with excellent stereoselectivity. Particularly promising for future applications is the fact that even the industrial side product trimethylamine can be used as a substrate. John Wiley and Sons Inc. 2022-01-25 2022-02-19 /pmc/articles/PMC9303398/ /pubmed/34936144 http://dx.doi.org/10.1002/chem.202103931 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Kaper, Tobias
Geik, Dennis
Fornfeist, Felix
Schmidtmann, Marc
Doye, Sven
Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines
title Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines
title_full Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines
title_fullStr Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines
title_full_unstemmed Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines
title_short Stereoselective Synthesis of Tertiary Allylic Amines by Titanium‐Catalyzed Hydroaminoalkylation of Alkynes with Tertiary Amines
title_sort stereoselective synthesis of tertiary allylic amines by titanium‐catalyzed hydroaminoalkylation of alkynes with tertiary amines
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303398/
https://www.ncbi.nlm.nih.gov/pubmed/34936144
http://dx.doi.org/10.1002/chem.202103931
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