5653-33-8Relevant articles and documents
Dithioacetal as a 1,1-zwitterion synthon. Synthesis of functionalized alkenes by the coupling of benzylic dithioacetals with another 1,1-zwitterion synthon
Tu, Hai-Yang,Liu, Yi-Hung,Wang, Yu,Luh, Tien-Yau
, p. 771 - 773 (2005)
Reaction of a dithioacetal sequentially with BuLi and alkyl bromide having an electron withdrawing substituent at the α-position followed by treatment with neutral alumina gives the corresponding olefination product in moderate to good yields.
Synthesis of 9-fluorenylidenes and 9,10-phenanthrenes through palladium-catalyzed aryne annulation by o-halostyrenes and o-halo allylic benzenes
Worlikar, Shilpa A.,Larock, Richard C.
supporting information; experimental part, p. 9132 - 9139 (2010/03/01)
(Chemical Equation Presented) A number of functionally substituted 9-fluorenylidenes and 9,10-phenanthrenes have been synthesized from substituted o-halostyrenes and o-halo allylic benzenes respectively in good yields by the palladium-catalyzed annulation
Reinvestigation on Thermal Cycloaddition of 1-Aryl-2-(9-fluorenylidene)-1-haloethylenes
Minabe, Masahiro,Yoshida, Masaaki,Saito, Seiji,Tobita, Keisuke,Toda, Takashi
, p. 2067 - 2070 (2007/10/02)
The thermal treatment of 1-bromo-2-(9-fluorenylidene)-1-phenylethylene afforded three different types of cycloaddition products.The 1-tolyl homolog showed similar trends, but the chloro analog gave only two types.These results suggest that reactions