135910-46-2Relevant academic research and scientific papers
Enantioselective Synthesis of Girolline
Commercon, A.,Paris, J. M.
, p. 4905 - 4906 (2007/10/02)
Girolline (RP 49532) is efficiently and enantioselectively synthesized from the aldol reaction of (R)-3-chloroacetyl-4-isopropyl-1,3-oxazolidin-2-one 2 and 1-triphenylmethylimidazole-4-carboxaldehyde 3 followed by reaction with aqueous ammonia and reducti
A diastereoselective synthesis of girolline
Commercon,Gueremy
, p. 1419 - 1422 (2007/10/02)
Girolline (RP 49532, 1), a new antitumour agent, was prepared in the racemic series using an oxidation-reduction sequence starting from (±)-erythro-β-chloro-γ-hydroxy- 1-triphenylmethyl-1H-4-imidazolepropanamine 3. The heterocyclic amino function was intr
DIASTEREOSELECTIVE CHLOROCYCLOFUNCTIONALIZATION OF N-ALLYLIC TRICHLOROACETAMIDES: SYNTHESIS OF AN ANALOGUE AND POTENTIAL PRECURSOR OF RP49532
Commercon, A.,Ponsinet, G.
, p. 3871 - 3874 (2007/10/02)
Treatment of (E)-N-cinnamyl trichloroacetamide with hypochlorous acid yielded trans-dihydro-oxazine 8 which was easily hydrolyzed to (+/-)-erythro-β-chloro-γ-hydroxy-γ-phenyl-propanamine 2.Applied to the imidazole series, this chlorocyclization gave 15, a
