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@article{1225845, author = {Shobeiri, Zohreh and Pourayoubi, Mehrdad and Nečas, Marek and Divjakovic, Vladimir and Babiak, Michal}, article_location = {NEW YORK}, article_number = {2}, doi = {http://dx.doi.org/10.1007/s13738-014-0479-6}, keywords = {LiF nano cubic; Thia-Michael addition; beta-Aryl-beta-mercapto ketones; Crystal structure; Ultrasound irradiation}, language = {eng}, issn = {1735-207X}, journal = {JOURNAL OF THE IRANIAN CHEMICAL SOCIETY}, title = {Sonochemical synthesis of lithium fluoride nano cubic as an active and simple catalyst for thia-Michael addition process: synthesis and structural characterization of beta-aryl-beta-mercapto ketones}, volume = {12}, year = {2015} }
TY - JOUR ID - 1225845 AU - Shobeiri, Zohreh - Pourayoubi, Mehrdad - Nečas, Marek - Divjakovic, Vladimir - Babiak, Michal PY - 2015 TI - Sonochemical synthesis of lithium fluoride nano cubic as an active and simple catalyst for thia-Michael addition process: synthesis and structural characterization of beta-aryl-beta-mercapto ketones JF - JOURNAL OF THE IRANIAN CHEMICAL SOCIETY VL - 12 IS - 2 SP - 245-255 EP - 245-255 PB - SPRINGER SN - 1735207X KW - LiF nano cubic KW - Thia-Michael addition KW - beta-Aryl-beta-mercapto ketones KW - Crystal structure KW - Ultrasound irradiation N2 - LiF nano cubic, with an average particle size of 21.6 nm, was synthesized sonochemically, using tetrabutylammonium fluoride as the fluoride source and characterized by SEM-EDX and XRD. This was applied, as a heterogeneous nano-catalyst, to synthesize some beta-aryl-beta-mercapto ketone derivatives via thia-Michael addition reactions with excellent yields at room temperature. In this catalytic system, the products of undesirable side reactions resulting from 1,2-addition, polymerization, bis-addition and oxidative coupling of thiols were not observed. The products were characterized by elemental analysis, IR, NMR and mass, and also single crystal X-ray determination for 3-(4-chlorophenylthio)-1,3-diphenylpropan-1-one, 1-phenyl-3-(phenylthio)-3-p-tolylpropan-1-one, 3-(p-tolylthio)- 1-phenyl-3-p-tolylpropan-1-one and 3-(4-chlorophenylthio)- 1-phenyl-3-p-tolylpropan-1-one. Following the recent search on the CSD, it is found that there is no report on the structure determination of [R-1]C[H][CH2C(O)R-2][S-Ar] beta-aryl-beta-mercapto ketones with the S-C6H5, S-C6H4-pCH(3) and S-C6H4-p-Cl segments (as S-Ar). ER -
SHOBEIRI, Zohreh, Mehrdad POURAYOUBI, Marek NEČAS, Vladimir DIVJAKOVIC and Michal BABIAK. Sonochemical synthesis of lithium fluoride nano cubic as an active and simple catalyst for thia-Michael addition process: synthesis and structural characterization of beta-aryl-beta-mercapto ketones. \textit{JOURNAL OF THE IRANIAN CHEMICAL SOCIETY}. NEW YORK: SPRINGER, 2015, vol.~12, No~2, p.~245-255. ISSN~1735-207X. Available from: https://dx.doi.org/10.1007/s13738-014-0479-6.
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