548483-75-6

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 548483-74-5 (3S,5S)-1-phenyl-7-octene-3,5-diol 
• 1398307-84-0 (4S,6S)-6-tert-Butyldimethylsilyloxy-8-phenyloct-1-en-4-ol 
• 1398308-08-1 C₁₈H₃₂O₃Si 
• 60340-28-5 (R)-1-phenyl-hex-5-en-3-ol 
• 60340-28-5 (S)-1-phenyl-5-hexen-3-ol 
• 104-53-0 3-phenyl-propionaldehyde 
• 261917-78-6 (S)-3-((tert-butyldimethylsilyl)oxy)-5-phenylpentanal 
• 1379822-84-0 (-)-(S)-1-phenyl-3-(tert-butyldimethylsilyloxy)-hex-5-ene 
• 887195-31-5 (S)-3-acetoxy-1-phenylhex-5-ene 
• 60340-28-5 1-phenylhex-5-en-3-ol 

Downstream Products

• 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 
• 485321-73-1 (R)-6-[(E)-3-((4S,6S)-2,2-Dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-propenyl]-5,6-dihydro-pyran-2-one 
• 548483-76-7 (E)-4-((4S,6S)-2,2-Dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-but-2-enal 

Relevant academic research and scientific papers

A chemoenzymatic asymmetric synthesis of (+)-strictifolione

A chemoenzymatic asymmetric synthesis of the title compound has been developed using an efficient lipase-catalyzed acylation and a chiral reagent-directed diastereoselective allylation as the key steps for incorporating the stereogenic centers. A cross me

Total synthesis of (+)-strictifolione.

[reaction: see text] The synthesis of (+)-strictifolione was achieved from 3-phenylproprionaldehyde by using enantioselective allyltitanations to control the stereogenic centers at C6, C4', and C6' and a cross-methathesis to control the configuration of t