66513-31-3Relevant academic research and scientific papers
Isolation of Novel Radical Cations from Hydroquinone Ethers. Conformational Transition of the Methoxy Group upon Electron Transfer
Rathore, Rajendra,Kochi, Jay K.
, p. 4399 - 4411 (2007/10/02)
Hydroquinone ethers as the bis-annulated derivatives R1-R3 are excellent electron donors by virtue of the facile oxidation to their radical cations R1.(1+), R2.(1+), and R3.(1+) that are readily isolable as unusually robus
The 1:1 and 2:1 adducts of cyclopentadiene with p-benzoquinone
Yates, Peter,Switlak, Krzysztof
, p. 1894 - 1900 (2007/10/02)
The exo-cis isomer (8) of the well-known endo-cis 1:1 adduct (4) of cyclopentadiene and p-benzoquinone has been obtained by heating the endo-cis-anti-cis-endo 2:1 adduct (13) with p-benzoquinone and also by haeting 4 alone.The exo-cis isomer of the 1:1 adduct (11) of cyclopentadiene and p-toluquinone has also been obtained for the first time.Heating of the 2:1 adduct 13 gives a mixture containing the endo-anti-exo isomer 15, the exo-anti-exo isomer 16, and 13.The structures of these two new isomers are assigned on the basis of (i) spectroscopic comparison with 13 and the known endo-syn-endo and endo-syn-exo isomers, 12 and 14; (ii) spectroscopic comparison of the corresponding tetrahydro compounds; and (iii) the conversion of tetrahydro 15 by oxidation and acetylation to the syn-hydroquinone diacetate 28, which is stereoisomeric with the anti-hydroquinone diacetate 25, prepared by similar treatment of tetrahydro 13,14, and 16.It is proposed that interconversion of the 1:1 adducts occurs via dissociation-recombination, interconversion of the tetrahydro 2:1 adducts occurs via enolization, while interconversion of the 2:1 adducts themselves can occur by both routes.
