Asymmetric Intramolecular C-H Insertion Promoted by Dirhodium(II) Carboxylate Catalyst Bearing Axially Chiral Amino Acid Derivatives.

Autor: Wen-jie Lu, Xu Pei, Takuya Murai, Takahiro Sasamori, Norihiro Tokitoh, Takeo Kawabata, Takumi Furuta
Předmět:
Zdroj: Synlett; 2017, Vol. 28 Issue 6, p679-683, 5p
Abstrakt: A dirhodium(II) carboxylate catalyst bearing axially chiral amino acid derivatives is prepared. X-ray crystal structure analysis reveals that four of the bridging ligands are aligned in a C2-symmetry-like conformation. This catalyst is effective in the asymmetric intramolecular C-H insertion of α-aryl-α-diazoacetates to α-aryl-β-substituted γ-lactones with a reasonable level of diastereo- and enantioselectivity, especially in the reaction of phenyl- and β-naphthyl-substituted substrates. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index