81120-67-4

Upstream product

• 80885-30-9 (E)-4-(benzyloxy)-2-buten-1-ol 
• 81132-12-9 (E)-3-((2S,3S)-3-Benzyloxymethyl-oxiranyl)-prop-2-en-1-ol 
• 114861-30-2 (S)-5-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-6-(phenylmethoxy)-2-hexen-1-ol 2,2-dimethylpropanoate 
• 114861-29-9 (S)-6-(phenylmethoxy)-2-hexene-1,5-diol 1-(2,2-dimethylpropanoate) 
• 114861-28-8 (S)-6-(phenylmethoxy)-2-hexene-1,5-diol 
• 114925-54-1 <2R-(2β,3α)>-3-<(phenylmethoxy)methyl>oxiranecarboxaldehyde 
• 78513-15-2 <2R-(2β,3α)>-3-<(phenylmethoxy)methyl>oxiranemethanol 
• 81096-94-8 ((2S,3R,2'R,3'S)-3'-Benzyloxymethyl-[2,2']bioxiranyl-3-yl)-methanol 
• 114925-55-2 (S)-5-<<(1,1-dimethylethyl)diphenylsilyl>oxy>-6-(phenylmethoxy)-2-hexen-1-ol 

Downstream Products

• 151140-37-3 ((4R,6S)-6-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-acetic acid 
• 92757-83-0 (3R,5S)-6-Benzyloxy-3,5-dihydroxy-hexanoic acid 
• 112497-22-0 (3S,5S)-6-<(benzyloxy)methyl>-4-<1-(tert-butyldiphenylsilyloxy)ethyl>-2,2-dimethyl-1,3-dioxacyclohexane 
• 112497-21-9 (4S,6S)-6-<(benzyloxy)methyl>-4-(2-hydroxyethyl)-2,2-dimethyl-1,3-dioxacyclohexane 
• 92757-18-1 (4R,6S)-6-(benzyloxy)methyl-4-hydroxy-tetrahydro-2-pyrone 
• 114861-34-6 2,4-dideoxy-6-O-<(1,1-dimethylethyl)diphenylsilyl>-3,5-O-(1-methylethylidene)-D-erythro-hexitol 1-(2,2-dimethylpropanoate) 
• 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 
• 114861-32-4 2,4-dideoxy-3,5-O-(1-methylethylidene)-6-O-(phenylmethyl)-D-erythro-hexitol 1-(2,2-dimethylpropanoate) 
• 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 
• 153025-58-2 (3S,5S)-6-(benzyloxy)-1-(tert-butyldiphenylsilyloxy)-3,5-dihydroxyhexane 
• 114861-31-3 2,4-dideoxy-6-O-(phenylmethyl)-D-erythro-hexitol 1-(2,2-dimethyl-propanoate) 

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

Synthesis of Saccharides and Related Polyhydroxylated Natural Products. 2. Simple Deoxyalditols

Asymmetric epoxidation of allylic alcohols followed by selective hydride reduction provides a new route to chiral 1,3-diols and 1,3,5-triols; one of the 1,3,5-triols (21) is also synthesized from D-glucose.