173142-87-5

Upstream product

• 100-44-7 benzyl chloride 
• 90093-98-4 (2S,3R,5S,6S)-2-isopropyloxy-3,5-dimethyl-6-<1(S)-methyl-2-hydroxyethyl>tetrahydropyran 
• 114144-80-8 (2S,3R,5S,6S)-6-<(2S)-1-benzyloxyprop-2-yl>-3,5-dimethyl-2-isopropoxytetrahydropyran 

Downstream Products

• 144534-83-8 benzyl 2-<(2S,3R,5S,6S)-6-<(2S)-1-tert-butyldimethylsilyloxyprop-2-yl>-3,5-dimethyl-2-hydroxytetrahydropyran-2-yl>acetate 
• 144534-84-9 benzyl 2-<(2S,3R,5S,6S)-3,5-dimethyl-2-hydroxy-6-<(2S)-1-oxoprop-2-yl>tetrahydropyran-2-yl>acetate 
• 172995-74-3 benzyl 2-<(2S,3R,5S,6S)-3,5-dimethyl-2-hydroxy-6-<(2S)-1-hydroxyprop-2-yl>tetrahydropyran-2-yl>acetate 

Relevant academic research and scientific papers

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