1: phenylacetylene With n-butyllithium in tetrahydrofuran T=-78°C; 0.5 h; 2: (Z)-diphenyl(β-phenylthiostyryl)selenonium trifluoromethanesulfonate in tetrahydrofuran T=-78°C; 5 h; Further stages.;
参考文献
Journal of Organic Chemistry, , vol. 65, # 26 p. 8893 - 8898
triethylaluminum; sulfur; triphenylphosphine; cobalt(II) 2,4-pentanedionate 1) toluene, -15 to -10 deg C, 5-10 min; 2) toluene, 130 deg C, 6 h; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
参考文献
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), , vol. 38, # 3.2 p. 581 - 586
Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, , # 3 p. 655 - 660
Ismailova, L. A.; Yusupov, D.; Akhmerov, K. M.; Kuchkarov, A. B.
Chemistry of Heterocyclic Compounds (New York, NY, United States), 1984 , vol. 20, # 3 p. 339
Khimiya Geterotsiklicheskikh Soedinenii, 1984 , vol. 20, # 3 p. 417
