118673-08-8Relevant academic research and scientific papers
Synthesis of 2-phosphonopyrroles via a one-pot RCM/oxidation sequence
Moonen, Kristof,Dieltiens, Nicolai,Stevens, Christian V.
, p. 4006 - 4009 (2007/10/03)
A four-step synthesis of 2-phosphonopyrroles is presented starting from suitable aldehydes. The key step in the synthesis involves a one-pot ring-closing metathesis/oxidation sequence of a functionalized α-aminoalkenyl phosphonate. Notwithstanding the pre
2-AZA-1,3-DIENES AS NOVEL PRECURSORS FOR THE SYNTHESIS OF N-UNSUBSTITUTED β-LACTAMS. A THREE STEP SYNTHESIS OF 4-ACETOXY-3-PHENOXY-2-AZETIDINONE
Georg, Gunda I.,Kant, Joydeep,He, Ping,Ly, Ana Maria,Lampe, Lynn
, p. 2409 - 2412 (2007/10/02)
2-Aza-1,3-dienes, prepared in excellent yields from aldehydes and readily available allylamine, were utilized to synthesize N-(1-propenyl)-β-lactams.Oxidative cleavage of the N-protecting group produced N-unsubstituted β-lactams. 4-Acetoxy-3-phenoxy-2-aze
