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Long-lived carbocations: Generation from 5,5,10,10-tetramethyl-5,10-dihydroindeno[2,1-a]indene, structure, and rearrangements Научная публикация

Журнал Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Вых. Данные Год: 2001, Том: 37, Номер: 9, Страницы: 1255-1258 Страниц : 4 DOI: 10.1023/A:1013167201820
Авторы Genaev AM 1 , Sal'nikov GE 1 , Shubin VG 1
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: According to the NMR data, protonation of 5,5,10,10-tetramethyl-5,10-dihydroindeno[2,1-a]indene in the system HSO3F-SO2ClF-CD2Cl2 at -80degreesC gives rise to long-lived 5,5,10,10-tetramethyl-2H-5,10-dihydroindeno[2,1-a]indenium ion which undergoes isomerization into 4b,5,10,10-tetramethyl-4b,5,9b,10-tetrahydroindeno[2,1-a]inden-5-yl cation on raising the temperature. On the basis of the data obtained for rearrangements of such carbocations an alternative mechanism has been proposed for the rearrangements of structurally related carbocations having a bicyclo[3.3.0]octane skeleton.
Библиографическая ссылка: Genaev A. , Sal'nikov G. , Shubin V.
Long-lived carbocations: Generation from 5,5,10,10-tetramethyl-5,10-dihydroindeno[2,1-a]indene, structure, and rearrangements
Russian Journal of Organic Chemistry. 2001. V.37. N9. P.1255-1258. DOI: 10.1023/A:1013167201820 WOS Scopus РИНЦ OpenAlex
Идентификаторы БД:
Web of science: WOS:000173634000012
Scopus: 2-s2.0-0035457338
РИНЦ: 13368970
OpenAlex: W2950581235
Цитирование в БД:
БД Цитирований
Web of science 2
Scopus 2
РИНЦ 2
OpenAlex 1
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