55533-86-3Relevant academic research and scientific papers
Practical synthesis of a potent hepatitis C virus RNA replication inhibitor
Bio, Matthew M.,Xu, Feng,Waters, Marjorie,Williams, J. Michael,Savary, Kimberly A.,Cowden, Cameron J.,Yang, Chunhua,Buck, Elizabeth,Song, Zhiguo J.,Tschaen, David M.,Volante,Reamer, Robert A.,Grabowski, Edward J. J.
, p. 6257 - 6266 (2007/10/03)
A practical, efficient synthesis of 1, a hepatitis C virus RNA replication inhibitor, is described. Starting with the inexpensive diacetone glucose, the 12-step synthesis features a novel stereoselective rearrangement to prepare the key crystalline furanose diol intermediate. This is followed by a highly selective glycosidation to couple the C-2 branched furanose epoxide with deazapurine.
Anthracyclinones. Part 5. Synthesis of Some Anthracyclinones and 4-Hydroxyanthracyclinones containing a Tertiary Methyl Carbinol Function in Ring A from D-Glucose Precursors
Ali, Zulficar,Qureshi, Shireen,Shaw, Gordon,Clercq, Erik de
, p. 2627 - 2636 (2007/10/02)
Reaction of 3-C-Methyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose (8a) with leucoquinizarin (2,3,4a,9a-tetrahydroanthracene-1,4,9,10-tetraone) (1a) in alkaline solution followed by aerial oxidation gave mainly (5S)-3-C-methyl 1,2-O-isopropylid
