88991-32-6Relevant articles and documents
UNUSUAL AMINO ACIDS. IV. ASYMMETRIC SYNTHESIS OF THIENYLALANINES
Doebler, Christian,Kreuzfeld, H.-J.,Krause, H. W.,Michalik, M.
, p. 1833 - 1842 (1993)
(Z)-2-N-Acylamino-3-thienyl-acrylic acids and thei esters were prepared by known procedures and hydrogenated to the corresponding optically active 2-N-acetyl(or benzoyl)-3-(2- or 3-thienyl)-alanines with optically yields up to 90percent using the rhodium complexes of 'PROPRAPHOS" 6a,b and O,N-bis(diphenylphosphino)-2-exo-hydroxy,3-endo-methylamino-norbornane 6c as chiral catalysts.Recrystallization and deacylation of the obtained amino acid derivatives yields the optically pure hydrochlorides of the thienylalanines as the free amino acids.
On the Synthesis of 3(5)-Carbomethoxy-4-hetarylpyrazoles
Cativiela, Carlos,Villegas, Maria D. Diaz de,Mayoral, Jose A.,Avenoza, Alberto,Roy, Miguel A.
, p. 851 - 855 (2007/10/02)
3(5)-Carbomethoxy-4-hetarylpyrazoles 3 can be obtained by the aromatization of the corresponding cis-3-benzamido-3-carbomethoxy-4-hetaryl-Δ1-pyrazolines 2 obtained by 1,3-dipolar cycloaddition of diazomethane with methyl Z-2-benzamido-3-hetarylpropenoates 1.An explanation, based on FMO theory, for the different reactivity of the dipolarophiles with diazomethane is given.