المؤلفون: Majid Mommahed Heravi (9225485), Ali Ayati (12001177), Mansoureh Daraie (6995462), Bahareh Tanhaei (12001201)

مصطلحات موضوعية: Organic Chemistry, Nuclear Chemistry, Computational Chemistry, Non-metal Chemistry, Nanochemistry and Supramolecular Chemistry, Optical Properties of Materials, Natural Products Chemistry, Organic Green Chemistry, Organic Chemistry not elsewhere classified, Quantum Chemistry, Organometallic Chemistry, Catalysts, Chitin, Chitosan, Energy dispersive spectroscopy, Fourier transform infrared spectroscopy, Scanning, electron microscopy, Aryl aldehydes, Energy dispersive X ray spectroscopy, Facile procedure, Magnetic chitosan, Novel catalysts, Novel nanocomposites, Refluxing condition, Three-components reactions, Silicon compounds

العلاقة: https://figshare.com/articles/journal_contribution/H4_W12SiO40_grafted_on_magnetic_chitosan_A_green_nanocatalyst_for_the_synthesis_of_1_2_4_triazolo_benzimidazolo_quinazolinone_derivatives/19069217Test

الإتاحة: https://doi.org/10.6084/m9.figshare.19069217.v1Test

المؤلفون: Mengtao Tian (9638785), Lei Wang (6656), Jin Wang (29560), Shuchang Zheng (9638788), Fudi Wang (158748), Ning Shao (1305756), Lele Wang (542468)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Ecology, Plant Biology, Chemical Sciences not elsewhere classified, ∼ 12 μm, negatively charged nanochannel, favorable retention rate, contaminative nanosheet synthesis, average lateral sizes, also confirmed using, low structural stability, precise molecular separation, performance membrane development, molecular separation, molecule separation, work shows, vmt membrane, ultrasonic bath, term stability, surface charge, sieving properties, scale production, practical applications, possible route, harsh environments, facile procedure, environmental applications, dye molecules

العلاقة: https://figshare.com/articles/journal_contribution/A_Two-Dimensional_Lamellar_Vermiculite_Membrane_for_Precise_Molecular_Separation_and_Ion_Sieving/18166652Test

الإتاحة: https://doi.org/10.1021/acssuschemeng.1c05951.s001Test

المؤلفون: Mohamadpour, Farzaneh

المساهمون: Apadana Institute of Higher Education

مصطلحات موضوعية: багатозамещені дигідропірол-2-они, октадегідрат алюмінію сульфату, екологічно безпечний та ефективний каталізатор, одностадійний синтез, багатокомпонентна реакція, polysubstituted dihydropyrrol-2-ones, aluminum sulfate octadecahydrate, eco-safe and efficient catalyst, one-pot and facile procedure, multi-component reaction

جغرافية الموضوع: Львів, Lviv

وصف الملف: 14-19; application/pdf; image/png

العلاقة: Chemistry & Chemical Technology, 1 (14), 2020; https://doi.org/10.1021/jm0102203Test; https://doi.org/10.1021/jo010828jTest; https://doi.org/10.1021/jm00060a012Test; https://doi.org/10.7164/antibiotics.47.851Test; https://doi.org/10.1021/jo050236rTest; https://doi.org/10.1021/jm0509400Test; https://doi.org/10.1021/jo00126a071Test; https://doi.org/10.1016/j.bmc.2007.05.052Test; https://doi.org/10.1016/j.bmc.2010.09.036Test; https://doi.org/10.1007/s11164-016-2565-0Test; https://doi.org/10.1007/s40995-016-0049-0Test; https://doi.org/10.1007/s13738-016-0871-5Test; https://doi.org/10.4067/s0717-97072018000103811Test; https://doi.org/10.1007/s40995-016-0122-8Test; https://doi.org/10.1021/co300148cTest; https://doi.org/10.1016/j.cclet.2013.10.010Test; https://doi.org/10.1016/j.tetlet.2012.03.046Test; https://doi.org/10.1021/cc900046fTest; https://doi.org/10.1007/s11164-012-0998-7Test; https://doi.org/10.1007/s13738-013-0222-8Test; https://doi.org/10.3184/174751912X13547952669204Test; https://doi.org/10.1007/s11164-015-2178-zTest; https://doi.org/10.1002/jccs.201200597Test; https://doi.org/10.1007/s11164-013-1364-0Test; https://doi.org/10.1007/s11164-017-2979-3Test; https://doi.org/10.1002/jhet.2352Test; [1] Borthwick A., Crame A., Ertl P. et al.: J. Med. Chem., 2002, 45, 1. https://doi.org/10.1021/jm0102203Test; [2] Li W., Lin S., Hsu N., Chern M.: J. Org. Chem., 2002, 67, 4702. https://doi.org/10.1021/jo010828jTest; [3] Lampe Y., Chou R., Hanna R. et al.: J. Med. Chem., 1993, 36, 1041. https://doi.org/10.1021/jm00060a012Test; [4] Shiozawa H., Takahashi S.: J. Antibiot., 1994, 47, 851. https://doi.org/10.7164/antibiotics.47.851Test; [5] Chen Y., Zeng D., Xie N., Dang Y.: J. Org. Chem., 2005, 70, 5001. https://doi.org/10.1021/jo050236rTest; [6] Grunwald C., Rundfeldt C., Lankau H. et al.: J. Med. Chem., 2006, 49, 1855. https://doi.org/10.1021/jm0509400Test; [7] Singh S., Goetz M., Jones E. et al.: J. Org. Chem., 1995, 60, 7040. https://doi.org/10.1021/jo00126a071Test; [8] Kawasuji T., Fuji M., Yoshinaga T. et al.: J. Bioorg. Med. Chem., 2007, 15, 5487. https://doi.org/10.1016/j.bmc.2007.05.052Test; [9] Zhang L., Tan Y., Wang N. et al. J. Bioorg. Med. 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Soc., 2018, 63, 3788. https://doi.org/10.4067/s0717-97072018000103811Test; [17] Lashkari M., Heydari R., Mohamadpour F.: Iran. J. Sci. Technol. Trans. Sci., 2018, 42, 1191. https://doi.org/10.1007/s40995-016-0122-8Test; [18] Lv L., Zheng S., Cai X., Chen Z., Zhu Q., Liu S.: ACS Comb. Chem., 2013, 15, 183. https://doi.org/10.1021/co300148cTest; [19] Sajadikhah S S., Maghsoodlou M T., Hazeri N.: Chin. Chem. Lett., 2014, 25, 58. https://doi.org/10.1016/j.cclet.2013.10.010Test; [20] Khan A., Ghosh A., Musawwer Khan M.: Tetrahedron Lett., 2012, 53, 2622. https://doi.org/10.1016/j.tetlet.2012.03.046Test; [21] Zhu Q., Jiang H., Li J. et al.: ACS Comb. Chem., 2009, 11, 685. https://doi.org/10.1021/cc900046fTest; [22] Sajadikhah S., Hazeri N.: Res. Chem. Intermed., 2014, 40, 737. https://doi.org/10.1007/s11164-012-0998-7Test; [23] Sajadikhah S., Hazeri N., Maghsoodlou M. et al. J. Iran. Chem. Soc., 2013, 10, 863. https://doi.org/10.1007/s13738-013-0222-8Test; [24] Sajadikhah S., Hazeri N., Maghsoodlou M.: J. Chem. Res., 2013, 37, 40. https://doi.org/10.3184/174751912X13547952669204Test; [25] Sajadikhah S., Maghsoodlou M., Hazeri N., Mohamadian-Souri S.: Res. Chem. Intermed., 2016, 42, 2805. https://doi.org/10.1007/s11164-015-2178-zTest; [26] Sajadikhah S., Hazeri N., Maghsoodlou M., Habibi-Khorassani S.: J. Chin. Chem. Soc., 2013, 60, 1003. https://doi.org/10.1002/jccs.201200597Test; [27] Sajadikhah S., Maghsoodlou M., Hazeri N.: Res. Chem. Intermed., 2015, 41, 2503. https://doi.org/10.1007/s11164-013-1364-0Test; [28] Kaur R., Gupta A., Kapoor K.: Res. Chem. Intermed., 2017, 43, 6099. https://doi.org/10.1007/s11164-017-2979-3Test; [29] Mohammadi A., Salman Taheri S., Amouzegar A.: J. Heterocyclic Chem., 2016, 53, 805. https://doi.org/10.1002/jhet.2352Test; [1] Borthwick A., Crame A., Ertl P. et al., J. Med. Chem., 2002, 45, 1. https://doi.org/10.1021/jm0102203Test; [2] Li W., Lin S., Hsu N., Chern M., J. Org. Chem., 2002, 67, 4702. https://doi.org/10.1021/jo010828jTest; [3] Lampe Y., Chou R., Hanna R. et al., J. Med. Chem., 1993, 36, 1041. https://doi.org/10.1021/jm00060a012Test; [4] Shiozawa H., Takahashi S., J. Antibiot., 1994, 47, 851. https://doi.org/10.7164/antibiotics.47.851Test; [5] Chen Y., Zeng D., Xie N., Dang Y., J. Org. Chem., 2005, 70, 5001. https://doi.org/10.1021/jo050236rTest; [6] Grunwald C., Rundfeldt C., Lankau H. et al., J. Med. Chem., 2006, 49, 1855. https://doi.org/10.1021/jm0509400Test; [7] Singh S., Goetz M., Jones E. et al., J. Org. Chem., 1995, 60, 7040. https://doi.org/10.1021/jo00126a071Test; [8] Kawasuji T., Fuji M., Yoshinaga T. et al., J. Bioorg. Med. Chem., 2007, 15, 5487. https://doi.org/10.1016/j.bmc.2007.05.052Test; [10] Maghsoodlou M., Heydari R., Mohamadpour F., Lashkari M., Iran. J. Chem. Chem. Eng., 2017, 36(4), 31.; [11] Maghsoodlou M., Heydari R., Lashkari M., Mohamadpour F., Indian J. Chem., 2017, 56 B, 160.; [12] Mohamadpour F., Maghsoodlou M., Heydari R., Lashkari M., Res. Chem. Intermed., 2016, 42, 7841. https://doi.org/10.1007/s11164-016-2565-0Test; [13] Mohamadpour F., Maghsoodlou M., Heydari R., Lashkari M., Iran. J. Sci. Technol. Trans. Sci., 2017, 41, 843. https://doi.org/10.1007/s40995-016-0049-0Test; [14] Mohamadpour F., Maghsoodlou M., Heydari R., Lashkari M., J. Iran. Chem. Soc., 2016, 13, 1549. https://doi.org/10.1007/s13738-016-0871-5Test; [15] Mohamadpour F., Maghsoodlou M., Heydari R., Lashkari M., Iran. J. Catal., 2016, 6, 127.; [16] Mohamadpour F., Lashkari M., Maghsoodlou M., Heydari R., J. Chil. Chem. Soc., 2018, 63, 3788. https://doi.org/10.4067/s0717-97072018000103811Test; [17] Lashkari M., Heydari R., Mohamadpour F., Iran. J. Sci. Technol. Trans. Sci., 2018, 42, 1191. https://doi.org/10.1007/s40995-016-0122-8Test; [18] Lv L., Zheng S., Cai X., Chen Z., Zhu Q., Liu S., ACS Comb. Chem., 2013, 15, 183. https://doi.org/10.1021/co300148cTest; [19] Sajadikhah S S., Maghsoodlou M T., Hazeri N., Chin. Chem. Lett., 2014, 25, 58. https://doi.org/10.1016/j.cclet.2013.10.010Test; [20] Khan A., Ghosh A., Musawwer Khan M., Tetrahedron Lett., 2012, 53, 2622. https://doi.org/10.1016/j.tetlet.2012.03.046Test; [21] Zhu Q., Jiang H., Li J. et al., ACS Comb. Chem., 2009, 11, 685. https://doi.org/10.1021/cc900046fTest; [22] Sajadikhah S., Hazeri N., Res. Chem. Intermed., 2014, 40, 737. https://doi.org/10.1007/s11164-012-0998-7Test; [24] Sajadikhah S., Hazeri N., Maghsoodlou M., J. Chem. Res., 2013, 37, 40. https://doi.org/10.3184/174751912X13547952669204Test; [25] Sajadikhah S., Maghsoodlou M., Hazeri N., Mohamadian-Souri S., Res. Chem. Intermed., 2016, 42, 2805. https://doi.org/10.1007/s11164-015-2178-zTest; [26] Sajadikhah S., Hazeri N., Maghsoodlou M., Habibi-Khorassani S., J. Chin. Chem. Soc., 2013, 60, 1003. https://doi.org/10.1002/jccs.201200597Test; [27] Sajadikhah S., Maghsoodlou M., Hazeri N., Res. Chem. Intermed., 2015, 41, 2503. https://doi.org/10.1007/s11164-013-1364-0Test; [28] Kaur R., Gupta A., Kapoor K., Res. Chem. Intermed., 2017, 43, 6099. https://doi.org/10.1007/s11164-017-2979-3Test; [29] Mohammadi A., Salman Taheri S., Amouzegar A., J. Heterocyclic Chem., 2016, 53, 805. https://doi.org/10.1002/jhet.2352Test; Mohamadpour F. Al2(SO4)3·18H2O as an Eco-Safe Catalyst Promoting Synthesis of Polysubstituted Dihydropyrrol-2-ones / Farzaneh Mohamadpour // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 14. — No 1. — P. 14–19.; https://ena.lpnu.ua/handle/ntb/55772Test

الإتاحة: https://doi.org/10.1021/jm0102203Test
https://doi.org/10.1021/jo010828jTest
https://doi.org/10.1021/jm00060a012Test
https://doi.org/10.7164/antibiotics.47.851Test
https://doi.org/10.1021/jo050236rTest
https://doi.org/10.1021/jm0509400Test
https://doi.org/10.1021/jo00126a071Test
https://doi.org/10.1016/j.bmc.2007.05.052Test
https://doi.org/10.1016/j.bmc.2010.09.036Test
https://doi.org/10.1007/s11164-016-2565-0Test

المؤلفون: Farzaneh Mohamadpour

المساهمون: Apadana Institute of Higher Education

مصطلحات موضوعية: General Chemical Engineering, одностадійний синтез, General Chemistry, eco-safe and efficient catalyst, багатокомпонентна реакція, multi-component reaction, Catalysis, one-pot and facile procedure, багатозамещені дигідропірол-2-они, polysubstituted dihydropyrrol-2-ones, Organic chemistry, екологічно безпечний та ефективний каталізатор, aluminum sulfate octadecahydrate, октадегідрат алюмінію сульфату

وصف الملف: application/pdf; image/png

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d146b6179a1f43fc7bb838f29d2e492Test
https://ena.lpnu.ua/handle/ntb/55772Test

المؤلفون: Tsiourvas, D, Tsetsekou, A, Kammenou, M-I, Boukos, N

مصطلحات موضوعية: Biomedical implants, Calcium phosphate phasis, Diaminobutane, Facile procedure, FTIR, Hydrothermally treated, Mean size, Molar ratio, Nanoparticle size distribution, Narrow size distributions, Physicochemical property, Poly(propylene imine), Potential applications, Room temperature, Synthesis conditions, XRD, TEM, Apatite, Calcium, Crystal growth, Dendrimers, Functional polymers, Hydroxyapatite, Nanorods, Propylene, Size distribution, Calcium phosphate

العلاقة: 94; 2023; 2029

الإتاحة: https://doi.org/10.1111/j.1551-2916.2010.04342.xTest