Reduction of 2,3,5-tri-O-benzyl-α (and β)-d-ribofuranosylethyne
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference17 articles.
1. J.G. Buchanan, A.D. Dunn, and A.R. Edgar, J. Chem. Soc. Perkin I, in the press
2. 2,3,5-Tri-O-benzyl-D-ribosyl and -L-arabinosyl Bromides
3. C-nucleoside studies. Part I. Synthesis of [2,3,5-tri-O-benzyl-α(and β)-D-ribofuranosyl]ethyne
4. Synthesis with partially benzylated sugars. XI. Synthesis of the anomeric 5,6-dimethyl-1-D-ribofuranosylbenz-imidazoles (ribazoles). Comparison of the condensation of 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide and 2,3,5-O benzyl-D-ribofuranosyl chloride with 5,6-dimethylbenzimidazole
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2. John Grant Buchanan;Advances in Carbohydrate Chemistry and Biochemistry;2013
3. Stereoselective synthesis of 1-deoxy-1-ethynyl-β-d-ribofuranose as a versatile scaffold;Tetrahedron Letters;2012-12
4. R;Dictionary of Carbohydrates;1998
5. Carbohydrates;Carbohydrates;1987
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