105545-16-2

Upstream product

• 129245-12-1 Benzoic acid (2S,3R,4S,5R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,4-dimethyl-heptyl ester 
• 128879-58-3 (1S,2R,4R,5R,9S,10R,13R,14R,15R,19S,20S)-13-Ethyl-4,14-dihydroxy-17-(4-methoxy-phenyl)-2,4,7,7,10,14,19,20-octamethyl-6,8,12,16,18-pentaoxa-tricyclo[13.3.1.1^5,9]icosan-11-one 
• 129245-14-3 (3S,4R,5S,6R,7S,8R)-7,8-Bis-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-6-(4-methoxy-benzyloxy)-3,5,7-trimethyl-1,1,1-triphenyl-decan-2-one 
• 129245-09-6 2,6-didesoxy-3-O-(p-methoxybenzyl)-4-O-methoxymethyl-2,4,6-tri-C-methyl-D-glucopyranose 
• 128879-55-0 (2R,4R,5S,6R)-4-[(S)-2-((S)-Benzenesulfinyl)-1-methyl-ethyl]-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethyl-silanyloxy)-1-methyl-butyl]-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxane 
• 128879-55-0 (2R,4R,5S,6R)-4-[(S)-2-((R)-Benzenesulfinyl)-1-methyl-ethyl]-6-[(1S,2R)-1,2-bis-(tert-butyl-dimethyl-silanyloxy)-1-methyl-butyl]-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxane 
• 124928-79-6 (4S,5R)-5-((R)-1-Benzyloxy-propyl)-2,2,5-trimethyl-[1,3]dioxolane-4-carbaldehyde 
• 105544-90-9 7-O-(t-butyldiphenylsilyl)-1,2-dideoxy-5,6-O-isopropylidene-4-C-methyl-keto-D-arabino-3-heptulose 
• 105544-88-5 (R)-2-[(4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-pentane-2,3-diol 
• 124928-74-1 (S)-2-[(4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-hydroxy-propionaldehyde 
• 105545-08-2 (2S,3R,4S,5R,6R,8R,9S,10S,11R,12R,13R)-2,4,6,8,10,12-Hexamethyl-6,12-bis-triethylsilanyloxy-pentadecane-1,3,5,9,11,13-hexaol 
• 105544-92-1 3-O-benzyl-1,2-dideoxy-4,5-isopropylidene-4-methyl-D-manno-heptitol 
• 124928-82-1 5-O-benzyl-1,2,6,7-tetradeoxy-2-iodo-3,4-O-isopropylidene-4-C-methyl-D-arabino-1-heptenitol 
• 105544-93-2 5-O-benzyl-1,6,7-trideoxy-3,4-O-isopropylidene-4-C-methyl-keto-D-arabino-2-heptulose 

Downstream Products

• 26754-37-0 erythronolide A 

Relevant academic research and scientific papers

STEREO-CONTROLLED SYNTHESIS OF ERYTHRONOLIDES A AND B FROM 1,6-ANHYDRO-β-D-GLUCOPYRANOSE (LEVOGLUCOSAN). SKELETON ASSEMBLY IN (C9 - C13) + (C7 - C8) + (C1 - C6) SEQUENCE

Stereospecific syntheses of erythronolides A and B have been accomplished starting from 1,6-anhydro-β-D-glucopyranose (levoglucosan) in a uniform synthetic sequence.