120666-58-2Relevant academic research and scientific papers
A new chiral pyrrolidine- and pyrrolidinone-ethanols for enantioselective addition of diethylzinc to arylaldehydes
Okuyama, Yuko,Nakano, Hiroto,Igarashi, Mayumi,Kabuto, Chizuko,Hongo, Hiroshi
, p. 635 - 643 (2007/10/03)
New chiral pyrrolidineethanols and unusual type of pyrrolidinoneethanol fused bicyclo[2.2.2]octane ring systems as backbones were synthesized and were used to the addition of diethylzinc to aromatic aldehydes to afford the secondary aryl alcohols leading
An Approach to the 3,8-Diazabicyclooctane Moiety of Naphthyridinomycin and Quinocarcin via 1,3-Dipolar Cycloaddition of Photochemically Generated Azomethine Ylides.
Garner, Philip,Sunitha, K.,Shanthilal, T.
, p. 3525 - 3528 (2007/10/02)
An attractive strategy for construction of the 3,8-diazabicyclooctane moiety of targets 1 and 2 involving the 1,3-dipolar cycloaddition of photochemical generated azomethine ylides is presented.
