103174-03-4Relevant academic research and scientific papers
Synthesis of novel enantiopure 4-hydroxypipecolic acid derivatives with a bicyclic β-lactam structure from a common 3-azido-4-oxoazetidine-2- carbaldehyde precursor
Alcaide, Benito,Almendros, Pedro,Luna, Amparo,Del Campo, Teresa Martinez
, p. 1635 - 1638 (2008/09/17)
(Chemical Equation Presented) Two different stereocontrolled accesses to new 4-hydroxypipecolic acid analogues with a bicyclic β-lactam structure have been developed by using intramolecular reductive amination or allenic hydroamination reactions in 2-azet
Studies on Lactams. 81. Enantiospecific Synthesis and Absolute Configuration of Substituted β-Lactams from D-Glyceraldehyde Acetonide
Wagle, Dilip R.,Garai, Chandra,Chiang, Julian,Monteleone, Michael G.,Kurys, Barbara E.,et al.
, p. 4227 - 4236 (2007/10/02)
Optically active 3,4-disubstituted 2-azetidinones have been prepared in good yield by the annelation of Schiff bases from D-glyceraldehyde acetonide with acid chlorides (or equivalent) and triethylamine.The utility of this enantiospecific synthesis was ex
