27262-02-8Relevant articles and documents
Synthesis and structure of chiral 2,6-bis[(2-carbamoyl- phenyl)carbamoyl]pyridine ligands
Yu, Qiang,Baroni, Timothy E.,Liable-Sands, Louise,Rheingold, Arnold L.,Borovik
, p. 6831 - 6834 (1998)
The synthesis and structure of a series of enantiomerically pure 2,6- bis[(2-carbamoylphenyl)carbamoyl]pyridine ligands (H22a-c) are described. Appended from the aryl groups are optically active groups which provide a chiral environment around
Catalytic reductive N-alkylation of anilines. Application to the synthesis of N-aryl aminoacid precursors
Fache, Fabienne,Valot, Frederic,Milenkovic, Alexandra,Lemaire, Marc
, p. 9777 - 9784 (2007/10/03)
Different anilines have been monoalkylated by reductive alkylation using ketones and α-ketoesters as alkylating agents with good isolated yields. This provided access to aminoacid derivatives. Diastereoselective experiments were also performed.