122030-57-3Relevant academic research and scientific papers
Acyclic stereoselection in the tertiary amine-catalysed addition of activated vinyl systems (Baylis-Hillman reaction) to protected chiral α-hydroxy and α-amino aldehydes
Manickum, Thavrin,Ross, Gregory H. P.
, p. 1 - 16 (2007/10/03)
The non chelation-controlled aldol-type addition of the ambident vinyl α anions derived from acrylic esters and methyl vinyl ketone to a series of protected chiral α-hydroxy and α-amino aldehydes has been investigated in order to assess some of the factors which contribute to the control of the diastereofacial selectivity.Whlist the α-methylene-β,γ-disubstituted carbonyl products showed a general preference for selectivity, some examples of syn predominance were made possible via a 'substituent tuning'approach.The observed diastereomer ratios have been interpreted in terms of the Felkin model and the Anh-Eisenstein proposals for 1,2-asymmetric induction.Simple steric effects appear to be as important as ?-orbital energies in the designation of the large 'anti group' for the application of these transition-state interpretations.Attempts to improve the overall induction via double diastereoselection approach, which combines the 1,5-induction of chiral acrylates with the 1,2-induction already present, were largely inconclusive.Methods for the routine NMR assignment of the relevant stereo-substructures have been assessed and the use of novel complementary technique is described.
Stereoselective addition of methyl acrylate to α-amino aldehydes
Manickum,Roos
, p. 2269 - 2274 (2007/10/02)
Variously N-protected α-aminoaldehydes exhibit reasonable diastereoselectivity in the Baylis-Hillman coupling with methyl acrylate to provide either primarily syn or anti α-methylene-β-hydroxy-γ-amino esters.
