120824-07-9Relevant academic research and scientific papers
Generation of 1,2-bisketenes from cyclobutene-1,2-diones by flash photolysis and ring closure kinetics
Allen, Annette D.,Colomvakos, Jim D.,Diederich, Fran?ois,Egle, Ian,Hao, Xiaokuai,Liu, Ronghua,Lusztyk, Janusz,Ma, Jihai,McAllister, Michael A.,Rubin, Yves,Sung, Kuangsen,Tidwell, Thomas T.,Wagner, Brian D.
, p. 12125 - 12130 (2007/10/03)
The interconversion of cyclobutene-1,2-diones (1) and 1,2-bisketenes (RC-C-O)2 has been surveyed for different combinations of substituents R = H, Me, t-Bu, Ph, Me3Si, CN, Cl, Br, R1O, alkynyl, and PhS. The bisketenes 2 have been generated by flash photolysis, and the kinetics of their conversion to 1 have been studied by time-resolved infrared and ultraviolet spectroscopy. The rate constants of the ring closure of 2 are correlated by the ketene stabilization parameters (SE) and with calculated barriers. The rate constant of ring closure of the di-tert-butyl bisketene 2g to cyclobutenedione 1g is only 40 times smaller than for the dimethyl analogue, showing a rather modest steric barrier. The quinoketene 2s has a fast rate of ring closure, but not as fast as anticipated on the basis of calculated geometric and thermodynamic factors. A lag in the attainment of aromatic stabilization in the transition structure for ring closure is a possible cause of this diminished reactivity.
Oxocarbons and Related Compounds; Part 16. Synthesis of 3-Alkylthio- and 3-Arylthio-3-cyclobutene-1,2-diones (S-Alkyl and S-Aryl Thiosemisquarates)
Schmidt, Arthur H.,Kuenz, Christian,Debo, Michael,Mora-Ferrer, Juan-Pablo
, p. 819 - 822 (2007/10/02)
The reaction of semisquaric chloride (1) with thiols 2 (X = H) has been investigated.In the presence of triethylamine (Method A) only moderate yields of S-alkyl thiosemisquarates 3a-d were obtained.Moderate to good yields of S-alkyl and S-aryl thiosemisqu
