144534-87-2

Upstream product

• 144534-85-0 dimethyl (3S)-3-benzyloxy-2-oxopentylphosphonate 
• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 172995-88-9 (4R,5R)-4,5-Bis-((S)-1-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolane 
• 172995-75-4 (3S,4R,5R,6S)-3,6-dibenzyloxyoctane-4,5-diol 
• 147255-18-3 (S)-2-Benzyloxy-butyric acid 
• 110352-57-3 (S)-(-)-methyl 2-benzyloxybutyrate 
• 80928-04-7 (S)-(-)-2-Benzyloxybutyraldehyde 

Downstream Products

• 144900-82-3 (2R,5S)-5-benzyloxy-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>heptan-4-one 
• 144606-48-4 (2S,5S)-5-benzyloxy-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>heptan-4-one 
• 144534-89-4 ((1R,2S)-2-Benzyloxy-1-ethyl-1-{(R)-2-[(S)-2-(4-methoxy-phenyl)-[1,3]dioxolan-4-yl]-propyl}-butoxy)-tert-butyl-dimethyl-silane 
• 144534-90-7 (2S,3R,5R,6S)-6-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-5-ethyl-2-(4-methoxy-benzyloxy)-3-methyl-octan-1-ol 
• 144534-80-5 (2S,3R,5R,6S)-6-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-5-ethyl-2-(4-methoxy-benzyloxy)-3-methyl-octanal 
• 172995-91-4 {(1R,2S)-2-Benzyloxy-1-[(R)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-propyl]-1-ethyl-butoxy}-tert-butyl-dimethyl-silane 
• 172995-78-7 (2S,3R,5R,6S)-6-Benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-5-ethyl-3-methyl-octane-1,2-diol 
• 144534-88-3 (2R,4R,5S)-5-Benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-ethyl-heptan-4-ol 

Relevant academic research and scientific papers

Stereoselective total synthesis of lysocellin, the representative polyether antibiotic of the lysocellin family. Part 1. Synthesis of C1-C9 and C16-C23 subunits

The C1-C9 (4) and C16-C23 subunits (9) of lysocellin (1), a representative polyether antibiotic, were synthesized stereoselectively from D-glucose and D-mannitol. Stereocontrolled hydroboration, Michael reaction, Grignard reaction, etc. were successfully

Total Synthesis of the Polyether Antibiotic Lysocellin. 1. Stereocontrolled Synthesis of the C1-C9 and C16-C23 Fragments

Stereocontrolled synthesis of two fragments corresponding to the C1-C9 (3) and C16-C23 parts (6) of lysocellin (1) using hydroboration, Wittig-Horner reaction, and Michael reaction in the key steps is described. Key Words: Polyether antibiotic; Stereocont