Диссертация (1150132), страница 27
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1. – 1997. – Vol. 18. – P. 2707-2712.138VII. БлагодарностиИсследования были проведены с использованием оборудования ресурсных центров«Магнитно-резонансные методы исследования», «Методы анализа состава вещества»,«Рентгенодифракционные методы исследования», «Ресурсный образовательный центр понаправлению химия» Научного парка СПбГУ. Финансирование предоставлено СанктПетербургским государственным университетом (грант №12.38.16.2011, 12.38.195.2014) иРоссийским научным фондом (грант №14-13-00126).Мы выражаем благодарность Александру Юльевичу Иванову, ведущему специалисту РЦ«Магнитно-резонансные методы исследования», за помощь и ценные советы при установленииструктур полученных соединений.139VIII.
Приложение8.1. Спектр 2D NOESY соединения 4а1408.2. Спектр 2D NOESY соединения 30f7.007.508.00ppm (t1)8.00ppm (t2)7.507.008.3. Спектр 2D NOESY соединения 31f1418.4. Спектр 2D NOESY соединения 33b1428.5. Спектр 2D NOESY соединения 34b1438.6. Спектр 2D NOESY соединения 33c8.7. Спектр 2D NOESY соединения 34c1448.8. Спектр 2D NOESY соединения 33d6.006.507.007.508.008.50ppm9.00(t1)8.50ppm (t2)8.007.507.001458.9.
Спектр 2D NOESY соединения 34d1468.10. Структура пиримидина 35l8.11. Структура пиримидина 35v8.12. Структура пиразолопиримидина 41с1478.13. Фрагмент спектра HMBC 1H-15N соединения 41a8.14. Фрагмент спектра HSQMBC 1H-15N соединения 41a148.
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