203-12-3Relevant articles and documents
High-Temperature Behavior of 1,8-Diethynylanthracene. Benzaceanthrylene, a Transient Intermediate for Cyclopentapyrene
Sarobe, Martin,Jenneskens, Leonardus W.
, p. 8247 - 8250 (1997)
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From phenylenes to acenes: Flash vacuum pyrolytic isomerization of angular [3]phenylene to benzo[ghi]fluoranthene
Matzger, Adam J.,Vollhardt, K. Peter C.
, p. 1415 - 1416 (1997)
The flash vacuum pyrolysis of angular [3]phenylene and bis(2-ethynylphenyl)ethyne produces benzo[ghi]fluoranthene and chrysene, respectively.
Use of external radical sources in flash vacuum pyrolysis to facilitate cyclodehydrogenation reactions in polycyclic aromatic hydrocarbons
Amick, Aaron W.,Martin, Sara E.
, p. 1338 - 1343 (2014/11/08)
A new process to facilitate the cyclodehydrogenation of polycyclic aromatic hydrocarbons (PAHs) in flash vacuum pyrolysis (FVP) using an external radical source is described. Using hexanes as an external radical source the conversion of various PAHs to their cyclodehydrogenated products is vastly increased. Various other volatile organic compounds were also examined to determine their ability to act as external radical sources in FVP.
Facile bucky-bowl synthesis by regiospecific cove-region closure by Hf elimination
Amsharov, K. Yu.,Kabdulov,Jansen, Martin
supporting information; experimental part, p. 4594 - 4597 (2012/06/30)
Building bowls: An effective intramolecular aryl-aryl coupling is the key step in rational fullerene synthesis and in synthesis of extended buckybowl structures. Such a process can be embodied very efficiently through quantitative HF elimination on active Al2O3. The process is characterized by an unprecedentedly high chemoselectivity and regiospecificity. Copyright
Aryl-aryl bond formation by flash vacuum pyrolysis of benzannulated thiopyrans
Amick, Aaron W.,Wakamiya, Atsushi,Scott, Lawrence T.
, p. 5119 - 5122 (2008/12/20)
(Chemical Equation Presented) In contrast to fully unsaturated 7-membered ring sulfur heterocycles (thiepines), some of which extrude sulfur and give the ring-contracted hydrocarbon even at room temperature in solution, benzannulated thiopyrans (6-membere