791609-51-3Relevant academic research and scientific papers
Low temperature dehydrogenation of α-indoline nucleosides
Chandra, Tilak,Zou, Shawn,Brown, Kenneth L.
, p. 7783 - 7786 (2004)
A variety of α-indole nucleosides are easily prepared from α-indoline nucleosides in excellent yield and at moderate temperature using manganese dioxide and molecular sieves in benzene or methylene chloride.
Direct glycosylation: Synthesis of α-indoline ribonucleosides
Chandra, Tilak,Brown, Kenneth L.
, p. 2071 - 2074 (2007/10/03)
A selective synthesis of α-anomers of indoline nucleosides is described. Ribonucleosides of indoline, dimethylindoline and 5-bromoindoline are readily prepared in good yield by reacting indoline bases directly with the protected sugar, 2,3-O-(1-methylethylidene) 5-O-(triphenylmethyl)-D-ribofuranose in dry ethanol or methylene chloride in presence of molecular sieves at 40-60°C.
