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Intermolecular Hydroaminoalkylation of Alkynes.
Kaper, Tobias; Fischer, Malte; Thye, Hermann; Geik, Dennis; Schmidtmann, Marc; Beckhaus, Ruediger; Doye, Sven.
Afiliação
  • Kaper T; Institut für Chemie, Universität Oldenburg, Carl-von-Ossietzky-Strasse 9-11, 26129, Oldenburg, Germany.
  • Fischer M; Leibniz-Institut für Katalyse e.V. (LIKAT), Albert-Einstein-Straße 29A, 18059, Rostock, Germany.
  • Thye H; Institut für Chemie, Universität Oldenburg, Carl-von-Ossietzky-Strasse 9-11, 26129, Oldenburg, Germany.
  • Geik D; Institut für Chemie, Universität Oldenburg, Carl-von-Ossietzky-Strasse 9-11, 26129, Oldenburg, Germany.
  • Schmidtmann M; Institut für Chemie, Universität Oldenburg, Carl-von-Ossietzky-Strasse 9-11, 26129, Oldenburg, Germany.
  • Beckhaus R; Institut für Chemie, Universität Oldenburg, Carl-von-Ossietzky-Strasse 9-11, 26129, Oldenburg, Germany.
  • Doye S; Institut für Chemie, Universität Oldenburg, Carl-von-Ossietzky-Strasse 9-11, 26129, Oldenburg, Germany.
Chemistry ; 27(23): 6899-6903, 2021 Apr 21.
Article em En | MEDLINE | ID: mdl-33481309
ABSTRACT
Intermolecular hydroaminoalkylation reactions of alkynes with secondary amines, which selectively give access to allylic amines with E configuration of the alkene unit, are achieved in the presence of titanium catalysts. Successful reactions of symmetrically substituted diaryl- and dialkylalkynes as well as a terminal alkyne take place with N-benzylanilines, N-alkylanilines, and N-alkylbenzylamines.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha