532402-37-2

Upstream product

• 464-72-2 tetraphenylethane-1,2-diol 
• 13292-87-0 dimethyl sulfide borane 

Downstream Products

• 532402-38-3 2-[3-(tert-butyl-dimethyl-silanyloxy)-propenyl]-4,4,5,5-tetraphenyl-[1,3,2]dioxaborolane 
• 1137765-93-5 (Rh(H)Cl(PPh₃)2)(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1137765-88-8 (norbornylene(-H))(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1137765-74-2 (4-MeOC₄H₄CH(Me))(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1137765-77-5 (4-MeOC₄H₄CH₂CH₂)(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1190639-22-5 9-(2-(4,4,5,5-tetraphenyl-1,3,2-dioxaborolan-2-yl)ethyl)-9H-carbazole 
• 1137765-86-6 (CH₃(CH₂)7)(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1137765-90-2 (CH₃C(O)(CH₂)4)(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1137765-83-3 (4-FC₄H₄CH₂CH₂)(4,4,5,5-tetraphenyl-1,3,2-dioxoborolane(-H)) 
• 1137765-80-0 C₃₅H₂₉BO₃ 
• 1515-95-3 p-ethylanisole 
• 532402-39-4 (E)-3-(4,4,5,5-Tetraphenyl-[1,3,2]dioxaborolan-2-yl)-prop-2-en-1-ol 

Relevant academic research and scientific papers

4,4,5,5-Tetraphenyl-1,3,2-dioxaborolane: A bulky borane for the transition metal catalysed hydroboration of alkenes

4,4,5,5-Tetraphenyl-1,3,2-dioxaborolane (HBBzpin, 3) has been prepared in high yield by the addition of H3B·SMe2 to benzopinacol. HBBzpin is a relatively stable solid that reacts with a variety of alkenes under catalytic conditions t

1,1,2,2-Tetraphenyl-1,2-ethanediol: A new protecting group for the synthesis of cyclopropylboronic esters

While enantiomerically pure auxiliaries and protecting groups for boronic acids are well established, much less attention has been paid to achiral derivatives. The commercially available benzpinacol (9) proved to yield highly stable boronic esters. The ne