1418147-91-7

Upstream product

• 1826-67-1 vinyl magnesium bromide 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 

Downstream Products

• 1418147-70-2 (R,E)-1-iodo-4-(1-phenylpenta-1,4-dien-3-yl)benzene 
• 1561175-68-5 1-(1-(cyclopent-1-en-1-yl)but-3-en-2-yl)-4-iodobenzene 
• 1561175-42-5 (R)-1-(1-(cyclopent-1-en-1-yl)but-3-en-2-yl)-4-iodobenzene 
• 1561175-57-2 C₁₅H₁₇I 
• 1561175-78-7 1-iodo-4-(5-methylhexa-1,5-dien-3-yl)benzene 
• 1561175-54-9 (R)-1-iodo-4-(5-methylhexa-1,5-dien-3-yl)benzene 
• 1561175-62-9 C₁₃H₁₅I 

Relevant academic research and scientific papers

Enantio- and Diastereodivergent Synthesis of Spirocycles through Dual-Metal-Catalyzed [3+2] Annulation of 2-Vinyloxiranes with Nucleophilic Dipoles

The development of efficient and straightforward methods for obtaining all optically active isomers of structurally rigid spirocycles from readily available starting materials is of great value in drug discovery and chiral ligand development. However, the

Synthesis of C5-allylindoles through an iridium-catalyzed asymmetric allylic substitution/oxidation reaction sequence of N-alkyl indolines

Iridium/Br?nsted acid cooperative catalyzed asymmetric allylic substitution reactions at the C5 position of indolines have been reported for the first time. The highly efficient protocol allows rapid access to various C5-allylated products in good to high