Regioselective glycosylation: synthesis of alpha-indoline nucleosides
Kenneth L Brown1, Tilak Chandra, Shawn Zou
1Department of Chemistry and Biochemistry, Ohio University, Athens, Ohio 45701, USA. brownk3@ohiou.edu
Nucleosides, Nucleotides & Nucleic Acids
|November 8, 2005
Abstract:
Novel indoline ribonucleosides with the alpha-N-glycoside configuration are synthesized with very high regioselectivity in 90-96%yield, using TMS protected indolines and 2,3-O-(1-methylethylidene)-5-O-(triphenylmethyl)-alpha/beta-D-ribofuranose. The structures of these ribonucleosides were elucidated with X-ray crystallography as well as 2D (NOESY, COSY, and HMQC) NMR spectroscopy.
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