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Synthesis of chiral boranes via asymmetric insertion of carbenes into B-H bonds catalyzed by the rhodium(I) diene complex.
Ankudinov, Nikita M; Komarova, Alina A; Podyacheva, Evgeniya S; Chusov, Denis A; Danshina, Anastasia A; Perekalin, Dmitry S.
Afiliação
  • Ankudinov NM; A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova str., 119334, Moscow, Russia. dsp@ineos.ac.ru.
  • Komarova AA; A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova str., 119334, Moscow, Russia. dsp@ineos.ac.ru.
  • Podyacheva ES; A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova str., 119334, Moscow, Russia. dsp@ineos.ac.ru.
  • Chusov DA; National Research University Higher School of Economics, 7 Vavilova str., 117312, Moscow, Russia.
  • Danshina AA; A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova str., 119334, Moscow, Russia. dsp@ineos.ac.ru.
  • Perekalin DS; National Research University Higher School of Economics, 7 Vavilova str., 117312, Moscow, Russia.
Chem Commun (Camb) ; 60(65): 8601-8604, 2024 Aug 09.
Article em En | MEDLINE | ID: mdl-39045825
ABSTRACT
Molecules with chiral boron atoms have been scarcely studied due to limited synthetic access. Herein, we report a new method for their synthesis via asymmetric insertion of arydiazoacetates into the B-H bonds of prochiral carbene-boranes NHC-BH2R. The reaction is catalyzed by the rhodium(I) complex with the chiral diene ligand tBu2-TFB, which can be conveniently prepared by diastereoselective coordination of the racemic diene with (S-Salox)Rh(CO)2. The target boranes were typically obtained in 75-90% yields with 90-95% ee.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article