Sciact
  • EN
  • RU

Carbocationic cyclizations: IX. Rearrangement of long-lived 4-(2-biphenylyl)-1,2,3,4-tetramethylcyclobutenyl cation into trans- and cis-4,5,6,6-tetramethyl-4,5,6-trihydrocyclopenta[j,k]phenanthren-5-yl cations Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2003, Volume: 39, Number: 9, Pages: 1301-1308 Pages count : 8 DOI: 10.1023/B:RUJO.0000010218.88703.55
Authors Bushmelev VA 1 , Genaev AM 1 , Osadchii SA 1 , Shakirov MM 1 , Shubin VG 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: According to the H-1 and C-13 NMR data, long-lived 4-(2-biphenylyl)-1,2,3,4-tetramethylcyclobutenyl cation generated by protonation of 3-(2-biphenylyl)-1,2,3-trimethyl-4-methylenecyclobutene in superacids undergoes cyclization which launches further rearrangements finally leading to formation of a mixture of trans- and cis-4,5,6,6-tetramethyl-4,5,6-trihydrocyclopenta[j,k]phenanthren-5-yl cations.
Cite: Bushmelev V. , Genaev A. , Osadchii S. , Shakirov M. , Shubin V.
Carbocationic cyclizations: IX. Rearrangement of long-lived 4-(2-biphenylyl)-1,2,3,4-tetramethylcyclobutenyl cation into trans- and cis-4,5,6,6-tetramethyl-4,5,6-trihydrocyclopenta[j,k]phenanthren-5-yl cations
Russian Journal of Organic Chemistry. 2003. V.39. N9. P.1301-1308. DOI: 10.1023/B:RUJO.0000010218.88703.55 WOS Scopus РИНЦ OpenAlex
Original: Бушмелев В.А. , Генаев А.М. , Осадчий С.А. , Шакиров М.М. , Шубин В.Г.
Реакции карбокатионной циклизации ix.‘перегруппировка "долговечного" 4-(2-бифенилил)-1,2,3,4-тетраметил цик лобутени л-катион а в транси цис-4,5,6,6-тетраметил4,5,6тригидроциклопента [j,k] фенантрен - 5 - и л - катионы
Журнал органической химии (RUSS J ORG CHEM+). 2003. Т.39. №9. С.1374-1381. РИНЦ
Dates:
Published print: Sep 1, 2003
Identifiers:
Web of science: WOS:000187950500016
Scopus: 2-s2.0-3843051153
Elibrary: 13445602
OpenAlex: W2952738016
Citing:
DB Citing
Web of science 6
Scopus 9
Elibrary 8
OpenAlex 10
Altmetrics: