30169-45-0Relevant articles and documents
Additivity of the Electronic Meta-Substituent Effect in 3,5-Disubstituted Cumyl Radicals Assessed by the EPR D Parameter of 1,3-Arylcyclopentane-1,3-diyl Triplet Diradicals
Adam, Waldemar,Harrer, Heinrich M.,Maas, Wiebke
, p. 7263 - 7265 (2007/10/03)
The D parameter (EPR zero-field splitting) of the 3,3′,5,5′-tetrasubstituted triplet diradicals 6 (X = X′ = H, NO2, CH3, OAc, OCH3, NH2, and OH) were determined in a MTHF matrix at 77 K and serves as a spectrosc
Electronic Substituent Effects on the Acid-Catalyzed + + 2> Cycloaddition of Isopyrazoles with Cyclopentadiene and the Photochemical and Thermal Denitrogenation of the Resulting 1,4-Diaryl-7,7-dimethyl-2,3-diazabicyclohept-2-ene Azoalk
Adam, Waldemar,Harrer, Heinrich M.,Nau, Werner M.,Peters, Karl
, p. 3786 - 3797 (2007/10/02)
Eight symmetrically disubstituted 3,5-diaryl-4,4-dimethylisopyrazoles 6 with para and meta substituents (OMe, Me, H, F, Cl, Br, CN, NO2) and two unsymmetrically para-substituted derivatives (OMe and NO2; Me and CO2Me) were synthesized from the correspondi
OXYGEN-ATOM TRANSFER REAGENTS: NEW, REACTIVE α-AZOHYDROPEROXIDES
Baumstark, A. L.,Dotrong, M.,Vasquez, P. C.
, p. 1963 - 1966 (2007/10/02)
3,4,4-Trimethyl-4,5-dihydro-5-hydroperoxy-3,5-diaryl-3H-pyrazoles, synthesized by autoxidation of the corresponding 3,4-dihydro-2H-pyrazoles, are a new type of cyclic α-azohydroperoxide which is of high reactivity in oxygen-atom transfer chemistry.