85523-39-3Relevant academic research and scientific papers
Selective synthesis of (Z)-chalcogenoenynes and (Z,Z)-1,4-bis-chalcogenbuta-1,3-dienes using PEG-400
Lara, Renata G.,Soares, Liane K.,Jacob, Raquel G.,Schumacher, Ricardo F.,Perin, Gelson
, p. 2046 - 2054 (2016/11/03)
We present here our results on the temperature controlled, selective hydrochalcogenation of 1,4-diorganyl-1,3-butadiynes with nucleophilic species of selenium, tellurium and sulfur generated in situ from the respective diaryl dichalcogenide and NaBH4
Hydrochalcogenation of symmetrical and unsymmetrical buta-1,3-diynes with diaryl dichalcogenides: Facile entry to (Z)-1-(organylchalcogeno)but-1-en-3-yne derivatives
Venkateswarlu, Cheerladinne,Chandrasekaran, Srinivasan
, p. 395 - 410 (2015/02/19)
This work describes an efficient and stereoselective method for the hydrothiolation and -selenation of buta-1,3-diyne derivatives using diaryl disulfides or diselenides, respectively. In the presence of rongalite (HOCH2SO2Na) and potassium carbonate, buta-1,3-diynes undergo stereoselective addition of the thiolate or selenide anion generated in situ from diaryl disulfides or diselenides to afford the corresponding (Z)-1-sulfanyl- or (Z)-1-selanylalk-1-en-3-yne derivatives, respectively. The reaction of buta-1,3-diynes with diaryl disulfides or diselenides at higher temperature (70 °C) gave a mixture of monothiolation/selenation and bisthiolation/selenation products in moderate to good yields.
Synthesis of (Z)-organylthioenynes using KF/Al2O 3/solvent as recyclable system
Alves, Diego,Sachini, Maraisa,Jacob, Raquel G.,Lenard?o, Eder J.,Contreira, Maria E.,Savegnago, Lucielli,Perin, Gelson
experimental part, p. 133 - 135 (2011/02/26)
PEG-400 and glycerol were successfully used as recyclable solvents for the synthesis of several organylthioenynes in good to excellent yields and high selectivity using solid supported catalyst (KF/Al2O3). This easy, general and impr
Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: Hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes
Dabdoub, Miguel J.,Dabdoub, Vania B.,Lenard?o, Eder J.,Hurtado, Gabriela R.,Barbosa, Sandro L.,Guerrero Jr., Palimécio G.,Nazário, Carlos E. D.,Viana, Luiz H.,Santana, Amanda S.,Baroni, Adriano C. M.
experimental part, p. 986 - 990 (2009/10/23)
Hcny BRAdrothiolation of l-organcny BRAlbuta-l,3-dicny BRAnes and 1,4-diorgancny BRAlbuta-l,3-dicny BRAnes with the sodium organcny BRAlthiolate anions, which were generated in situ bcny BRA reacting diphencny BRAl and dibutcny BRAl disulfide with NaBHsu
INVESTIGATION IN THE REACTION OF BIACETYLENE DERIVATIVES. XLV. THIYLATION OF MONOSUBSTITUTED AND DISUBSTITUTED DIYNES WITH THIOPHENOL IN LIQUID AMMONIA
Levanova, E. P.,Volkov, A. N.,Volkova, K. A.
, p. 55 - 57 (2007/10/02)
The addition of thiophenol to monosubstituted biacetylene in ammonia solution takes place regiospecifically and stereospecifically at the terminal acetylene bond without a catalyst.Thiophenol reacts with disubstituted biacetylenes in the presence of alkal
