Biofunctional chemistry and reactivity of biogenic acrolein for cancer diagnosis and therapy and therapeutic purposes. Previously, we discovered 1,3-dipolar
cycloaddition between aryl azides and acrolein
Arylidene-Imidazolones and Their Acyclic Analogue as Fluorescent Sensors of Metal Ions.
Methods: The formation of imines with the following [2+3]-
cycloaddition and recycling. The use
Pentamethine cyanine dyes with alkynyl group as perspective structure for conjugation with targeting moietyUspenskaia A.A.,
Doroshenko I.A.,
Popovicheva K.A.,
Shmychkov N.V.,
Pryakhina E.V.,
Shafikov R.R.,
Skvortsov D.A.,
Beklemishev M.K.,
Zaborova O.V.,
Podrugina T.A.,
Machulkin A.E.,
Beloglazkina E.K. -alkyne
cycloaddition reaction, that possesses promising photochemical properties (Φfl = 0,49). As an example of usage
Homo-Diels-Alder reaction of a very inactive diene, bicyclo[2,2,1]hepta-2, 5-diene, with the most active dienophile, 4-phenyl-1,2,4-triazolin-3,5-dione. Solvent, temperature, and high pressure influence on the reaction rate-Diels-Alder
cycloaddition reactions of the very active hetero-dienophile, 4-phenyl-1,2,4-triazolin-3,5-dione (1