153255-49-3

Upstream product

• 153255-48-2 (R)-6-Benzyloxy-hex-2-yne-1,5-diol 
• 14618-80-5 (R)-benzyl glycidol 
• 80885-30-9 (E)-4-(benzyloxy)-2-buten-1-ol 
• 78469-85-9 (2S,3S)-4-benzyloxy-2,3-epoxy-1-butanol 
• 127909-66-4 (2R,3S)-3-Benzyloxymethyl-oxirane-2-carbaldehyde 

Downstream Products

• 106862-36-6 (3R,5R)-6-Benzyloxy-hexane-1,3,5-triol 
• 106799-18-2 3,5-dideoxy-6-O-<(1,1-dimethylethyl)dimethylsilyl>-2,4-O-(1-methylethylidene)-1-O-(phenylmethyl)-D-erythro-hexitol 
• 153324-80-2 (R)-1-Benzyloxy-3-((2R,3S)-3-phenylsulfanylmethyl-oxiranyl)-propan-2-ol 
• 153324-77-7 (R)-1-Benzyloxy-3-((2S,3R)-3-phenylsulfanylmethyl-oxiranyl)-propan-2-ol 
• 153255-54-0 (4R,6R)-6-Benzyloxymethyl-4-hydroxy-tetrahydro-pyran-2-one 
• 153324-79-9 (R)-1-Benzyloxy-3-((2R,3R)-3-hydroxymethyl-oxiranyl)-propan-2-ol 
• 153255-50-6 (R)-1-Benzyloxy-3-((2S,3S)-3-hydroxymethyl-oxiranyl)-propan-2-ol 

Relevant academic research and scientific papers

Diastereodivergent synthesis of optically active trans- and cis-6-benzyloxymethyl-4-hydroxytetrahydro-2-pyrones via 3-hydroxyalkenyl phenyl sulfides

A diastereodivergent synthesis of optically active trans- and cis-6-benzyloxymethyl-4-hydroxytetrahydro-2-pyrones has been developed via 3-hydroxyalkenyl phenyl sulfides by employing base-induced cleavage of the glycidyl phenyl sulfide functionality as th

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