745058-28-0

Upstream product

• 17376-04-4 2-phenethyl iodide 

Downstream Products

• 745058-49-5 {(E)-(R)-1-allyl-4-[(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]-but-2-enyloxy}-tert-butyldimethylsilane 
• 745058-36-0 tert-butyl-{2-[(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]ethoxy}-dimethylsilane 
• 745058-38-2 (4R,6S)-4-(2-iodoethyl)-2,2-dimethyl-6-phenethyl-[1,3]dioxane 
• 548483-78-9 acrylic acid (E)-(R)-1-allyl-4-{(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl}-but-2-enyl ester 
• 548483-77-8 (E)-(R)-7-((4S,6S)-2,2-Dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-hepta-1,5-dien-4-ol 
• 485321-85-5 5-{2-[(4R,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]-ethylsulfonyl}-1-phenyl-1H-tetrazole 
• 485321-90-2 5-{2-[(4R,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]-ethylsulfanyl}-1-phenyl-1H-tetrazole 
• 485321-86-6 (4S,6S)-4-{(E)-3-[(2R,6R)-6-isopropoxy-3,6-dihydro-2H-pyran-2-yl]-allyl}-2,2-dimethyl-6-phenethyl-[1,3]dioxane 
• 485321-74-2 2-{(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl}-ethanol 
• 745058-30-4 (4S,6S)-4-[2-(tert-butyldimethylsilanyloxy)ethyl]-2,2-dimethyl-6-phenethyl-[1,3]dioxan-5-one 

Relevant academic research and scientific papers

Efficient asymmetric syntheses of (+)-strictifolione

The asymmetric synthesis and a formal asymmetric synthesis of (+)-strictifolione are described. As key step in both approaches the Julia-Kocienski olefination to create an E-configured alkene was used. The anti-1,3-diol moiety was synthesized by employing