138723-62-3Relevant academic research and scientific papers
Enantiomerically pure dihydropyrimidinones as reagents and auxiliaries for asymmetric synthesis
Chu, Kent S.,Negrete, George R.,Konopebki, Joseph P.,Lakner, Frederick J.,Woo, Nam-Tae,Olmstead, Marilyn M.
, p. 1800 - 1812 (2007/10/02)
We report herein full experimental details of the synthesis, structure, and reactivity of (R)- and (S)-2-tert-butyl-l-carbomethoxy-2,3-dihydropyrimidin-4(lH)-one (1). The synthesis employs asparagine as the starting material and provides 1 in 55% yield without the need for Chromatographic purification. The structure of 1, as determined by X-ray crystallographic analysis, demonstrates significant pyramidalization at the C4 (carbonyl) and N1 centers, with little evidence of conjugation of Nl with the αβ,-unsaturated (vinylogous urea) system. In contrast, compound 11 [2-tert-butyl-3-((S)-O-methylmandeloyl)-2,3-dihydropyrimidin-4(lH)-one] shows strong coupling of Nl to the αβ,-unsaturated system, as evidenced by changes in bond lengths and torsional angles. Compound 1 has proven useful as a reagent for the synthesis of enantiomerically pure β-aryl-β-amino acids. The key step in this protocol is the palladium-catalyzed conjugate addition of aryl iodides to 1. Evidence is presented to support a mechanism for this reaction that involves an unprecedented transannular hydride transfer into the palladium coordination sphere. In additional experiments, 1 has been employed as an auxiliary for the synthesis of enantiomerically pure α-substituted carboxylic acids. The crystalline properties of 1 and many of its derivatives allow for simplified purification procedures to be utilized.
ASYMMETRIC ALKYLATIONS OF N-ACYL DIHYDROPYRIMIDINONES
Negrete, George R.,Konopelski, Joseph P.
, p. 105 - 108 (2007/10/02)
Enantiomerically pure dihydropyrimidin-4-one 1 has been employed as a chiral auxiliary for enantioselective alkylation reactions.Acylation of 1, followed by enolate formation, alkylation and acyl cleavage, affords α-alkylated carboxylic acids in high chemical yield and enantiomeric purity.
