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62
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V.42. N2. P.115-132. DOI: 10.1134/S1068162016020084
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63
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Rakhmanova M.E.
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Synthesis and cytotoxic activity of usnic acid cyanoethyl derivatives
Russian Chemical Bulletin. 2016.
V.65. N2. P.566-569. DOI: 10.1007/s11172-016-1338-7
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64
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Zakharenko A.
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Journal of Natural Products. 2016.
V.79. N11. P.2961-2967. DOI: 10.1021/acs.jnatprod.6b00979
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65
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Shtro A.A.
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Derivatives of usnic acid inhibit broad range of influenza viruses and protect mice from lethal influenza infection
Antiviral Chemistry and Chemotherapy. 2015.
V.24. N3-4. P.92-98. DOI: 10.1177/2040206616636992
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66
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Luzina O.A.
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Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
Chemistry of Natural Compounds. 2015.
V.51. N4. P.646-651. DOI: 10.1007/s10600-015-1376-7
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Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
Medicinal Chemistry Research. 2015.
V.24. N7. P.2926-2938. DOI: 10.1007/s00044-015-1348-2
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Chemistry of Natural Compounds. 2014.
V.50. N2. P.266-271. DOI: 10.1007/s10600-014-0928-6
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Bioorganic and Medicinal Chemistry. 2014.
V.22. N24. P.6826-6836. DOI: 10.1016/j.bmc.2014.10.033
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Синтез новых производных (+)-усниновой кислоты с флавоновым остовом
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Russian Chemical Bulletin. 2013.
V.62. N1. P.212-216. DOI: 10.1007/s11172-013-0031-3
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Sokolov D.N.
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V.48. N3. P.379-384. DOI: 10.1007/s10600-012-0257-6
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Chemistry of Natural Compounds. 2012.
V.48. N3. P.385-391. DOI: 10.1007/s10600-012-0258-5
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75
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Polovinka M.P.
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Secondary metabolites of the lichen Cladonia stellaris
Chemistry of Natural Compounds. 2012.
V.48. N3. P.392-395. DOI: 10.1007/s10600-012-0259-4
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V.81. N8. P.747-768. DOI: 10.1070/RC2012v081n08ABEH004245
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Medicinal Chemistry. 2012.
V.8. N5. P.883-893. DOI: 10.2174/157340612802084225
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78
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V.22. N23. P.7060-7064. DOI: 10.1016/j.bmcl.2012.09.084
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79
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V.47. N2. P.203-205. DOI: 10.1007/s10600-011-9882-8
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