Sharp difference in the rate of formation and stability of the Diels–Alder reaction adducts with 2, 3‐dicyano‐1, 4‐benzoquinone and N‐phenylimide‐1, 4‐benzoquinone‐2, 3‐dicarboxylic acid

Authors: Kiselev, Vladimir D., Kolesnikova, Anastasia O., Shulyatiev, Alexey A., Dinikaev, Ildar F., Kornilov, Dmitry A.

Source: International journal of chemical kinetics. 53(12):1306-1313

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100133138959.0x000001&indx=1&recIds=ETOCvdc_100133138959.0x000001

High pressure influence on the Diels–Alder reaction volume in the solid phase at pressure up to 7000 bar and in solution

Authors: Kornilov, Dmitry A., Dinikaev, Ildar F., Kiselev, Vladimir D.

Source: High pressure research. 39(4):640-654

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100094521099.0x000001&indx=1&recIds=ETOCvdc_100094521099.0x000001

Sharp difference in the rate of formation and stability of the Diels–Alder reaction adducts with 2,3‐dicyano‐1,4‐benzoquinone and N‐phenylimide‐1,4‐benzoquinone‐2,3‐dicarboxylic acid.

Authors: Kiselev, Vladimir D.¹, vkiselev.ksu@gmail.com, Kolesnikova, Anastasia O.¹, Shulyatiev, Alexey A.¹, Dinikaev, Ildar F.¹, Kornilov, Dmitry A.¹

Source: International Journal of Chemical Kinetics; Dec2021, Vol. 53 Issue 12, p1306-1313, 8p

Diels‐Alder reaction rate in the solid state and the evidence of the location of molecular complexes between the reagents on the reaction pathway.

Authors: Kiselev, Vladimir D.¹, vkiselev.ksu@gmail.com, Kolesnikova, Anastasia O.¹, Dinikaev, Ildar F.¹, Shulyatiev, Alexey A.¹, Klimovitskii, Alexander E.¹, Kornilov, Dmitry A.¹

Source: International Journal of Chemical Kinetics; Feb2021, Vol. 53 Issue 2, p207-212, 6p