75501-29-0

Upstream product

• 124-38-9 carbon dioxide 
• 591-51-5 phenyllithium 
• 150799-26-1 α-bromo-(1,1,3,3-tetramethyl-2-indanylidene)methane 
• 100-44-7 benzyl chloride 
• 5689-12-3 1,1,3,3-tetramethylindane-2-one 
• 75501-26-7 2-Benzyl-1,1,3,3-tetramethyl-2-indanol 

Downstream Products

• 75501-28-9 2-(α-bromobenzylidene)-1,1,3,3-tetramethylindane 
• 4705-87-7 1,2,3,3-tetramethyl-1H-indene 
• 100-52-7 benzaldehyde 
• 75501-31-4 2-Benzyl-1-brommethyliden-2,3,3-trimethylindan 
• 75501-32-5 2-Benzyl-2,3,3-trimethyl-1-methylenindan 
• 75501-30-3 2-(α-Brombenzyl)-1-brommethyliden-2,3,3-trimethylindan 

Relevant academic research and scientific papers

Carbenoid chain reactions through proton, deuteron, or bromine transfer from unactivated 1-bromo-1-alkenes to organolithium compounds

(Chemical Equation Presented) The deceptively simple vinylic substitution reactions Alk2C=CA-Br + RLi → Alk2C=CA-R + LiBr (A = H, D, or Br) occur via an alkylidenecarbenoid chain mechanism (three steps) without transition metal catal

On the Formation and Reactivity of Di-tert-alkyl Substituted Phenylalkenes

Molecular rearrangements occur during the attempted syntheses of α-bromo-β,β-di-tert-alkylstyrenes; the resulting structures are elucidated.A hydrocarbon dimer with allenic structure accompanies the formation of the Grignard reagent from an α-bromostyrene