128032-99-5

Upstream product

• 128032-98-4 C₁₉H₂₀ 
• 128032-98-4 C₁₉H₂₀ 

Downstream Products

• 128033-07-8 (Z)-(1R,3S)-1,7-Diphenyl-hept-4-ene-1,3-diol 
• 128033-07-8 (E)-(1R,3S)-1,7-Diphenyl-hept-4-ene-1,3-diol 
• 128033-14-7 (1S,2S)-1-((4S,6R)-2,2-Dimethyl-6-phenyl-[1,3]dioxan-4-yl)-1-iodo-4-phenyl-butan-2-ol 
• 128033-14-7 1-((4S,6R)-2,2-Dimethyl-6-phenyl-[1,3]dioxan-4-yl)-1-iodo-4-phenyl-butan-2-ol 
• 128033-13-6 (4R,6S)-2,2-Dimethyl-4-phenyl-6-((E)-4-phenyl-but-1-enyl)-[1,3]dioxane 
• 128033-15-8 Acetic acid (1R,3R,5S)-3,5-diacetoxy-1,7-diphenyl-heptyl ester 
• 103654-27-9 (S)-1-((4R,6R)-2,2-Dimethyl-6-phenyl-[1,3]dioxan-4-yl)-4-phenyl-butan-2-ol 
• 103654-25-7 (+/-)-yashabushitriol 
• 128033-13-6 (4R,6S)-2,2-Dimethyl-4-phenyl-6-((Z)-4-phenyl-but-1-enyl)-[1,3]dioxane 

Relevant academic research and scientific papers

Stereochemical studies on the preparation and subsequent reductive cleavage of 1,2-dioxolanes. Application to the synthesis of (±)-yashabushitriol

(E)-Selective oxygenation of 1,2-disubstituted alkenylcyclopropanes, and subsequent SmI2 mediated cleavage of the 1,2-dioxolane products with retention of stereochemistry, leads to a concise synthesis of the plant metabolite (±)-yashabushitriol.