The reactivity of thionaphtheno[3,2-b]pyrrole Научная публикация
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Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230 |
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| Вых. Данные | Год: 1968, Том: 17, Номер: 1, Страницы: 176-178 Страниц : 3 DOI: 10.1007/BF00914664 | ||
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Реферат:
By comparing the reactivity indices calculated by the molecular-orbit method, we conclude that in thionaphtheno[3,2-blpyrrole, electrophilic substitution must take place preferentially in position 2. © 1968 Consultants Bureau.
Библиографическая ссылка:
Shkurko O.P.
The reactivity of thionaphtheno[3,2-b]pyrrole
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1968. V.17. N1. P.176-178. DOI: 10.1007/BF00914664 Scopus РИНЦ
The reactivity of thionaphtheno[3,2-b]pyrrole
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1968. V.17. N1. P.176-178. DOI: 10.1007/BF00914664 Scopus РИНЦ
Даты:
| Опубликована в печати: | 1 янв. 1968 г. |
Идентификаторы:
| Scopus | 2-s2.0-34250523025 |
| РИНЦ | 30914548 |
| OpenAlex | W2003854775 |