74457-36-6

Upstream product

• 84107-76-6 (3E)-1,4-diphenylbut-3-en-1-ol 
• 74-88-4 methyl iodide 
• 74457-33-3 E-1,4-diphenyl-3-buten-1-one N-tosylhydrazone 
• 17572-77-9 (3E)-1,4-diphenylbut-3-en-1-one 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 591-50-4 iodobenzene 
• 401513-63-1 2-((E)-4-Methoxy-4-phenyl-but-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 
• 67-56-1 methanol 
• 74457-35-5 trans-1,4-diphenyl-4-diazobut-1-ene 
• 74457-37-7 exo-3,6-diphenyl-1,2-diazabicyclo<3.1.0>hex-2-ene 
• 74457-33-3 (E)-1,4-diphenyl-3-buten-1-one N-tosylhydrazone 

Relevant academic research and scientific papers

1-Silyl-1-boryl-2-alkenes: Reagents for stereodivergent allylation leading to 4-oxy-(E)-1-alkenylboronates and 4-oxy-(Z)-1-alkenylsilanes

Silylboryl reagents for organic synthesis: 1-silyl-1-boryl-2-alkenes (2) were prepared efficiently by gem-silylborylation of α-chloroallyllithium compounds from (dimethylphenylsilyl) (pinacolato)borane (1; see scheme, LDA = lithium diisopropylamide) and w

An unusual example of a 1,1-cycloaddition reaction of a diazoalkane

Thermolysis of the sodium salt of E-1,4-diphenyl-3-buten-1-one N-tosylhydrazone gave rise to the corresponding diazoalkane which undergoes a subsequent 1,1-cycloaddition reaction to produce 3,6-diphenyl-1,2-diazabicyclo[3.1.0]hex-2-ene.