38255-97-9Relevant academic research and scientific papers
Thermal isomerization of cis,anti,cis-tricyclo[6.3.0.02,7]undec- 3-ene to endo-tricyclo[5.2.2.02,6]undec-8-ene
Baldwin, John E.,Bogdan, Andrew R.,Leber, Phyllis A.,Powers, David C.
, p. 5195 - 5197 (2005)
(Chemical Equation Presented) The gas-phase thermal isomerization of cis,anti,cis-tricyclo[6.3.0.02,7]undec-3-ene (1) to endo-tricyclo[5.2.2.02,6]undec-8-ene (2) at 315°C occurs cleanly through a symmetry-forbidden [1,3] suprafacial,retention (sr) pathway.
Reductive Rearrangement with Hydride Transfer of Linearly and Angularly Fused Triquinanes
Kakiuchi, Kiyomi,Ue, Masaki,Kumanoya, Shuichi,Takeuchi, Hideyuki,Tobe, Yoshito,Odaira, Yoshinobu
, p. 1479 - 1482 (2007/10/02)
Relationship between linearly and angularly fused triquinanes is elucidated by reductive rearrangements with hydride transfer of tricyclo2,6>undecan-1-ol, tricyclo1,5>undecan-6-ols, and tricyclo1,5>undecan-11-ol.
Acid-Catalyzed Rearrangements of - and Propellanes, Tricyclo1,5>undecanes, and Tricyclo1,5>undecanes
Kakiuchi, Kiyomi,Ue, Masaki,Wakaki, Itsuyo,Tobe, Yoshito,Odaira, Yoshinobu,et al.
, p. 281 - 287 (2007/10/02)
Acid-catalyzed rearrangements of propellanols 2x and 2n, propellanol (3b), tricyclo1,5>-undecanes 4b-d and 5, and tricyclo1,5>undecanes 6a,b were studied.Tricycloundecanes 4d and 6b rearranged under CF3S
