139404-44-7Relevant academic research and scientific papers
Diastereoface-discrimination reaction of lithium or titanium ester enolates with a chiral imine leading to stereodivergent synthesis of β-lactams
Fujisawa, Tamotsu,Ukaji, Yutaka,Noro, Tomohiro,Date, Kengo,Shimizu, Makoto
, p. 5629 - 5638 (2007/10/02)
Diastereoselective addition reaction of ester enolates to a chiral imine possessing (4S, 5S)-4,5-dimethoxymethyl-2-methyl-1,3-dioxolane ring as a chiral auxiliary is reported, in which varying metal enolates resulted in the selective formation of (4S)- or
Highly diastereoselective synthesis of β-lactams by addition of titanium enolates of 2-pyridyl thioesters to chiral imines
Annunziata,Cinquini,Cozzi,Cozzi
, p. 1113 - 1116 (2007/10/02)
Addition of titanium enolates of 2-pyridyl thioesters to chiral imines derived from alkoxy aldehydes occurs with good diastereofacial control, and opens a simple access to important carbapenem antibiotics.
