200949-98-0Relevant academic research and scientific papers
Total syntheses of novel dideoxynucleoside analogues using chiral amino acids
Balayiannis,Karigiannis,Gatos,Papaioannou,De Clercq
, p. 6191 - 6194 (2007/10/03)
N-Tritylated L- and D-methionine and L-glutamic acid were used to obtain novel chiral iso-dideoxynucleoside analogues incorporating a tetrahydrofuranyl or a tetrahyropyranyl ring as the pseudosugar part, and at positions 2 and 3 of the ring an hydroxyethyl group and thymine or adenine, respectively. (C) 2000 Elsevier Science Ltd.
(3aR, 7aS)-N-triphenylmethyl-1,2,3,3a,5,6,7,7a-octahydropyrano[3,2-b]-pyrrol-2-one
Nastopoulos, Vassilios,Gourgioti, Ourania,Balayiannis, George,Karigiannis, George,Papaioannou, Dionissios,Kavounis, Constantin
, p. 1971 - 1973 (2007/10/03)
The title compound, C26H25NO2, is one of the two main products formed when an inseparable mixture of the diastereomeric (2R,3S)- and (2S,3S)-3-triphenylmethyl-aminooxinan-2-ylacetic acids is treated with N,N′-dicyclohexylc
