172995-75-4

Upstream product

• 172995-88-9 (4R,5R)-4,5-Bis-((S)-1-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolane 
• 100-44-7 benzyl chloride 

Downstream Products

• 80928-04-7 (S)-(-)-2-Benzyloxybutyraldehyde 
• 110352-57-3 (S)-(-)-methyl 2-benzyloxybutyrate 
• 144534-85-0 dimethyl (3S)-3-benzyloxy-2-oxopentylphosphonate 
• 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 
• 147255-18-3 (S)-2-Benzyloxy-butyric acid 
• 144534-87-2 (1E,4S)-4-benzyloxy-1-((4S)-2,2-dimethyl-1,3-dioxolan-4-yl)hex-1-en-3-one 

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