79386-75-7Relevant academic research and scientific papers
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,
Synthetic Studies of Rifamycins. IV. The Synthesis of Rifamycin Ansa-chain Compound Using Carbohydrate
Nakata, Masaya,Takao, Hideaki,Ikeyama, Yutaka,Sakai, Toshiya,Tatsuta, Kuniaki,Kinoshita, Mitsuhiro
, p. 1749 - 1756 (2007/10/02)
3-O-Benzyl-2,4,7-trideoxy-5,6-O-isopropylidene-2,4-di-C-methyl-L-glycero-D-galacto-heptose (6) was synthesized through 16 steps from 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-altropyranoside (7).The condensation of 6 with methyl 2,4,6,7-tetradeoxy-6-lithio
