943902-73-6

Upstream product

• 943901-45-9 (+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate 
• 949583-79-3 (E)-methyl (4-(trityloxy)but-2-en-1-yl)carbonate 

Downstream Products

• 107080-45-5 (S)-(+)-β-vinyl-γ-butyrolactone 
• 1373344-89-8 (3S)-3-[(trityloxy)methyl]pent-4-en-1-ol 
• 1373344-96-7 methyl (2E,6R,8Z,10E)-6-[[(triphenylmethyl)oxy]methyl]-dodeca-2,8,10-trienoate 
• 1373344-94-5 methyl (2E,6R,8E,10E)-6-[[(triphenylmethyl)oxy]methyl]-dodeca-2,8,10-trienoate 
• 1373344-90-1 1-phenyl-5-[[(3S)-3-[(trityloxy)methyl]pent-4-en-1-yl]thio]-1H-tetrazole 
• 1373344-87-6 C₂₅H₂₄O₂ 
• 1373344-91-2 1-phenyl-5-[[(3S)-3-[(trityloxy)methyl]pent-4-en-1-yl]-sulfonyl]-1H-tetrazole 
• 1373344-93-4 trityl (2S,4Z,6E)-2-vinylocta-4,6-dien-1-yl ether 
• 1373344-92-3 trityl (2S,4E,6E)-2-vinylocta-4,6-dien-1-yl ether 

Relevant academic research and scientific papers

Enantioselective Iridium-catalyzed allylic alkylations - Improvements and applications based on salt-free reaction conditions

Simplified procedures for the Ir-catalyzed asymmetric allylic alkylation reaction are described that often allow substitution products to be obtained with ≥99% ee. Applications to syntheses of important chiral building blocks, such as the Taniguchi lacton