1021245-67-9Relevant articles and documents
Enantioselective synthesis of arylglycine derivatives by direct C-H oxidative cross-coupling
Wei, Xiao-Hong,Wang, Gang-Wei,Yang, Shang-Dong
, p. 832 - 835 (2015)
A new method for the synthesis of chiral α-amino acid derivatives by enantioselective C-H arylation of N-aryl glycine esters with aryl boric acids in the presence of a chiral Pd(ii)-catalyst has been developed. This work successfully integrates the direct C-H oxidation with asymmetric arylation and exhibits excellent enantioselectivity. This journal is
A 4 - phenyl quinoline compound, preparation method and application thereof (by machine translation)
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Paragraph 0055, (2017/08/31)
The invention discloses a 4 - phenyl quinoline compound, its preparation method and application, the invention of the 4 - phenyl quinoline compound to, its structure (I) shown in the diimmonium: Wherein R1 Is - OH, - Cl, - OCH3 Or -
Functionalizing glycine derivatives by direct C-C bond formation
Zhao, Liang,Li, Chao-Jun
supporting information; experimental part, p. 7075 - 7078 (2009/04/07)
(Chemical Equation Presented) Come on glycine: Two different types of glycine derivatives are α-functionalized using cross-dehydrogenative- coupling (CDC) reactions. The method allows the efficient attachment of a malonate or aromatic alkyne group on the α-position of the glycine derivatives under very mild conditions.