106862-35-5

Upstream product

• 114861-18-6 3-deoxy-5-O-<(1,1-dimethylethyl)diphenylsilyl>-D-xylofuranose 
• 19493-09-5 Methylenetriphenylphosphorane 
• 532-20-7 D-xylofuranose 
• 114861-15-3 5-O-<(1,1-dimethylethyl)diphenylsilyl>-1,2-O-(1-methylethylidene)-α-D-xylofuranose 3-(O-phenylthiocarbonate) 
• 114861-14-2 1,2-O-isopropylidene-5-O-(t-butyldiphenylsilyl)-α-D-xylofuranose 
• 106799-13-7 3-deoxy-5-O-<(1,1-dimethylethyl)diphenylsilyl>-1,2-O-(1-methylethylidene)-α-D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 

Downstream Products

• 114861-19-7 <4S-(4β,6β)>-6-ethenyl-4-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>-2,2-dimethyl-1,3-dioxane 
• 106799-14-8 2,3-dideoxy-6-O-<(1,1-dimethylethyl)diphenylsilyl>-3,5-O-(1-methylethylidene)-1-O-(phenylmethyl)-D-erythro-hexitol 
• 114861-20-0 2,3-dideoxy-6-O-<(1,1-dimethylethyl)diphenylsilyl>3,5-O-(1-methylethylidene)-D-erythro-hexitol 
• 106799-15-9 3,5-dideoxy-2,4-O-(1-methylethylidene)-6-O-(phenylmethyl)-L-erythro-hexose 
• 114861-21-1 2,3-dideoxy-3,5-O-(1-methylethylidene)-1-O-(phenylmethyl)-D-erythro-hexitol 

Relevant academic research and scientific papers

Total Synthesis of Amphoteronolide B and Amphotericin B. 1. Strategy and Stereocontrolled Construction of Key Building Blocks

The retrosynthetic analysis and strategy for the total synthesis of amphotericin B (1) and amphoteronolide B (2) is discussed.Focusing on subtle and repeated structural units, a retrosynthetic scheme was constructed that led to the recognition of readily