351024-48-1Relevant academic research and scientific papers
Efficient synthesis of functionalized 4,5-benzotropones by regioselective cyclization of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with phthalic dialdehyde
Langer,Albrecht
, p. 526 - 528 (2001)
The reaction of 1,3-bis(trimethylsiloxy)-1,3-butadienes with phthalic dialdehyde resulted in regioselective formation of functionalized 4,5-benzotropones.
Synthesis of 4,5-Benzotropones by Cyclization of 1,3-Bis-Silyl Enol Ethers with 1,2-Dialdehydes
Albrecht, Uwe,Van Nguyen, Thi Hong,Langer, Peter
, p. 3417 - 3424 (2007/10/03)
The cyclization of 1,3-bis-silyl enol ethers or (2,4 -dioxobutylidene)triphenylphosphoranes with phthalic dialdehyde allowed a convenient synthesis of a variety of 4,5-benzotropones. The hydrogenation of benzotropones afforded functionalized benzocycloheptanones which were transformed into tricyclic butenolides.
