98039-08-8Relevant academic research and scientific papers
Chiral Synthesis of Polyketide-derived Natural Products. Part 5. Synthesis of a Chiral Segment Corresponding to the C-1-C-5 Unit of Erythromycin A from D-Glucose
Oikawa, Yuji,Nishi,Takao,Yonemitsu, Osamu
, p. 19 - 26 (2007/10/02)
As a right-hand segment with three consecutive chiral centres corresponding to the C-1-C-5 unit of erythromycin A (1), (2S,3R,4S)-3,5-isopropylidenedioxy-2,4-dimethylpentanal (32) was synthesized from D-glucose (5) by application of MPM (4-methoxybenzyl)
A CHIRAL SYNTHESIS OF 3,5,7-TRI-O-BENZYL-1,4,6-TRIDEOXY-4,6-DI-C-METHYL-keto-L-ido-2-HEPTULOSE, A SYNTHETIC SEGMENT OF THE C-1 - C-6 PORTION OF ERYTHRONOLIDE A
Kinoshita, Mitsuhiro,Ohsawa, Naoki,Gomi, Shuichi
, p. 5 - 24 (2007/10/02)
3,6-Dideoxy-1,2-O-isopropylidene-3-C-methyl-α-D-glucofuranose (9) was prepared from methyl 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-glucopyranoside via 3-deoxy-1,2-O-isopropylidene-3-C-methyl-α-D-glucofuranose (5) in 61percent yield.The key intermediates,
