Помогите, пожалуйста, скачать несколько эльзивировских статей:
1) Vellaisamy Sridharan, Carmen Avendaño and J. Carlos Menéndez. Convenient, two-step synthesis of 2-styrylquinolines: an application of the CAN-catalyzed vinylogous type-II Povarov reaction. Tetrahedron. V.65. #10. 2009. P. 2087-2096.
Код: Выделить всё
http://dx.doi.org/10.1016/j.tet.2008.12.077
2) Walaa A.E. Omar and Osmo E.O. Hormi. Synthesis of 4-(2-arylvinyl)-8-hydroxyquinolines via anhydrous Heck coupling reaction and the PL properties of their Al complexes. Tetrahedron. V.65. #22. 2009. P. 4422-4428.
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http://dx.doi.org/10.1016/j.tet.2009.03.028
3) Minoo Dabiri, Peyman Salehi, Mostafa Baghbanzadeh, Maryam Shakouri Nikcheh. A new and efficient one-pot procedure for the synthesis of 2-styrylquinolines. Tetrahedron Letters. V.49. #37. 2008. P. 5366-5368.
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http://dx.doi.org/10.1016/j.tetlet.2008.06.054
4) Robert Musiol, Josef Jampilek, Vladimir Buchta, Luis Silva, Halina Niedbala, Barbara Podeszwa, Anna Palka, Katarzyna Majerz-Maniecka, Barbara Oleksyn, Jaroslaw Polanski. Antifungal properties of new series of quinoline derivatives. Bioorganic & Medicinal Chemistry. V.14. #10. 2006. P. 3592-3598.
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http://dx.doi.org/10.1016/j.bmc.2006.01.016
5) Robert Musiol, Josef Jampilek, Katarina Kralova, Des R. Richardson, Danuta Kalinowski, Barbara Podeszwa, Jacek Finster, Halina Niedbala, Anna Palka, Jaroslaw Polanski. Investigating biological activity spectrum for novel quinoline analogues. Bioorganic & Medicinal Chemistry. V.15. #3. 2007. P. 1280-1288.
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http://dx.doi.org/10.1016/j.bmc.2006.11.020
6) Marie Normand-Bayle, Christophe Bénard, Fatima Zouhiri, Jean-François Mouscadet, Hervé Leh, Claire-Marie Thomas, Gladys Mbemba, Didier Desmaële, Jean d’Angelo. New HIV-1 replication inhibitors of the styryquinoline class bearing aroyl/acyl groups at the C-7 position: Synthesis and biological activity. Bioorganic & Medicinal Chemistry Letters. V.15. #18. 2005. P. 4019-4022.
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http://dx.doi.org/10.1016/j.bmcl.2005.06.036
