106288-35-1Relevant academic research and scientific papers
DEGENERATE REARRANGEMENTS OF 5-ARYLTHIO- AND 5-ARYLSELENO-1,2,3,4,5-PENTAMETHYL-1,3-CYCLOPENTADIENES
Borodkin, G. I.,Susharin, E. P.,Shakirov, M. M.,Shubin, V. G.
, p. 2131 - 2139 (2007/10/02)
The kinetics of the degenerate rearrangements of 5-R-1,2,3,4,5-pentamethyl-1,3-cyclopentadienes (R = C6H5S, C6F5S, C6H5Se, C6F5Se), which take place by a 1,2-shift of the group R, were studied by the dynamic PMR method.A comparison was made of the kinetic data on the 1,2-shifts of the H atom and CH3, C6H5, NO2, C6F5S, and C6F5Se groups in 5-R-1,2,3,4,5-pentamethyl-1,3-cyclopentadienes and in the "long-lived" carbocations in terms of the "reactivity-selectivity" principle.
Heteroatom-directed π-facial diastereoselection in diels-alder cycloadditions of plane-nonsymmetric cyclopentadienes
Macaulay,Fallis
, p. 1136 - 1144 (2007/10/02)
The synthesis of a series of pentamethylcyclopentadienes bearing stereogenic C-5 heteroatom substituents and their reactions in [4 + 2] cycloadditions with maleic anhydride and/or N-phenylmaleimide are described. Cyclopentadienes (13, 14, 6, 7, and 1) containing the substituents OH, OCH3, NH2, NHAc, and C1 reacted to form syn adducts preferentially. In contrast, with compound 8 (SH) only slight syn discrimination was observed, while the facial selectivity was reversed with other sulfur substituents (SCH3, SPh, SCH2Ph, SOCH3, SO2CH3) (compounds 9, 3, 2, 10, and 11), and anti adducts were the major or exclusive products. This behavior is consistent with the σ donor ability of the C-X versus the C-C bond so that cycloaddition occurs preferentially anti to the best donor due to hyperconjugation of this antiperiplanar σ bond with the developing incipient bond(s).
