36912-18-2Relevant academic research and scientific papers
Synthesis, charge distribution, and dimerization behavior of lithium alkynylselenolates
Pietschnig, Rudolf,Merz, Klaus,Schaefer, Sven
, p. 169 - 174 (2005)
The reactivity of alkynyl lithium compounds toward elemental gray selenium yields alkynylselenolates, which show significant interaction with the lithium counter ions, depending on solvent polarity and the electronic nature of the adjacent organic substit
Synthesis of CIS and trans-2,6-diphentyl-1,4-diselena-fulvenes from phenyiacetylene with selenium and base under PTC-Ultrasound conditions
Wang, Jin-Xian,Zhao, Kai
, p. 1617 - 1622 (2007/10/03)
A convenient and simple method for the synthesis of cis-and trans- 2,6-diphenyl- 1, 4-diselenafulvenes is described. The process involves the reaction of phenylacetylene with sodium hydroxide and selenium at 45-50°C and under PTC-Untrasound conditions to
REACTIONS OF CHALCOGENS WITH ACETYLENES. V. REACTIONS OF METALLIC SELENIUM WITH PHENYLACETYLENES
Amosova, S. V.,Potapov, V. A.,Kashik, A. S.,Gusarova, N. K.,Sinegovskaya, L. M.,et al.
, p. 470 - 475 (2007/10/02)
A method for the production of Z-2-benzylidene-4-phenyl-1,3-diselenole was worked up on the basis of an investigation into the effect of the process parameters on the yields of the products from the reaction of metallic selenium with phenylacetylene.
Some Transformations of 2-Methylene-1,3-diselenoles
Lakshmikantham, M. V.,Jackson, Yvette A.,Cava, Michael P.
, p. 3529 - 3532 (2007/10/02)
2-Benzylidene-4-phenyl-1,3-diselenole (5) was transformed into the green nitroso derivative 7 and the red phenylazo derivative 8 by reaction with NO+ and PHN2+ ions, respectively.Although the parent heterocycle 10 failed to give such
