149832-38-2

Upstream product

• 149832-36-0 2-Bromo-3-((R)-1-hydroxy-ethyl)-N-methoxy-N-methyl-benzamide 
• 149832-34-8 2-Bromo-N,N'-dimethoxy-N,N'-dimethyl-isophthalamide 
• 149832-35-9 3-Acetyl-2-bromo-N-methoxy-N-methyl-benzamide 
• 151603-30-4 2-bromobenzene-1,3-dicarboxylic acid dichloride 
• 22433-91-6 2-bromoisophthalic acid 
• 75-16-1 methylmagnesium bromide 
• 149832-37-1 2-Bromo-3-((R)-1-ethoxy-ethyl)-N-methoxy-N-methyl-benzamide 

Downstream Products

• 149832-39-3 2,6-bis(1-(R)-ethoxyethyl)bromobenzene 
• 149832-40-6 C₁₅H₂₁F₃O₅SSe 
• 149832-33-7 bis<2,6-bis(1-(R)-ethoxyethyl)phenyl> diselenide 
• 149857-05-6 (R)-1-[2-Bromo-3-((R)-1-ethoxy-ethyl)-phenyl]-ethanol 

Relevant academic research and scientific papers

Asymmetric Selenomethoxylation of Olefins Involving a Chiral C2 Symmetrical Electrophilic Organoselenium Reagent

A new chiral C2 symmetrical organoselenium reagent has been synthesized; this compound, in the presence of methanol, reacts with high facial selectivity with olefins to afford the anti selenomethoxylated adducts in very good yields.