80396-17-4Relevant academic research and scientific papers
Acid controlled generation of indanes and oxazolines from β-hydroxyarylethanamide
Suresh, Rajendran,Muthusubramanian, Shanmugam,Boominathan, Muthusamy,Manickam, Govindaswamy
supporting information, p. 2315 - 2320 (2013/06/26)
Simple and efficient protocols for the construction of substituted indanes and oxazolines through intramolecular cyclization of β- hydroxyarylethanamide using trifluoromethanesulfonic acid and titanium tetrachloride in 1,2-dichloroethane respectively have
β-Amino alcohols from amino acids: Chelation control via Schiff bases
Polt,Peterson
, p. 4985 - 4986 (2007/10/02)
Sequential addition of iBu2AlH and RLi or RMgX to Schiff base esters derived from amino acids provides a simple route to β-amino alcohols. The reaction procedes without racemization, and with high threo selectivity. Several representative sphingosines are synthesized.
Preparation, reduction chimique et electrochimique d'α-nitrostyrylcetones - synthese d'heterocycles azotes
Marcot, Bernard,Rabaron, Alain,Viel, Claude,Bellec, Christian,Deswarte, Stephane,Maitte, Pierre
, p. 1224 - 1234 (2007/10/02)
Nitration of styryl ketones with nitrogen peroxide leads to the corresponding α-nitroethylenic ketones in good yield.However, the presence of methoxy groups involves a nitration on the aromatic nucleus.LiAlH4 reduction of α-nitrostyrylketones yields the c
