Page 23 - НАУЧНЫЕ ОТКРЫТИЯ: МЕЖДИСЦИПЛИНАРНЫЕ АСПЕКТЫ

Международная научно-практическая конференция

(Allium cepa L.) // Natural product research. — 2018. — V. 32. —

P. 1193‒1197.

3. Mloston G., Heimgartner H. In Targets in heterocyclic systems;

chemistry and properties // Societa chimica Italiana. — 2005. — V. 9. —

P. 141‒157.

4. Tsuchihashi G., Yamauchi M., Ohno A. Thiocarbonyl compounds

as potential scavengers of carbon radicals // Bulletin of the chemical

society of Japan. — 1970. — V. 43. — P. 968.

5. Hejmanowska J., Jasinski M., Mloston G., Albrecht L. Taming of

thioketones: the first asymmetric thia-Diels-Alder reaction with thioketones

as heterodienophiles // European journal of organic chemistry. — 2017. —

V. 2017. — P. 950‒954.

6. Rohr U., Schatz J., Sauer J. Thio- and selenocarbonyl compounds

as “superdienophiles” in [4+2] cycloadditions // European journal of

organic chemistry. — 1998. — V. 1998. — P. 2875‒2883.

7. Metzner P. In Organosulfur сhemistry I. Topics in сurrent

сhemistry // Springer. 1999. — V. 204. — P. 127‒181.

8. Breu J., Hocht P., Rohr U., Schatz J., Sauer J. Thiocarbonyl

сompounds in [4+2] сycloadditions: preparative aspects // European journal

of organic chemistry. 1998. — V. 1998. — P. 2861‒2873.

9. Kiselev V.D., Kornilov D.A., Lekomtseva I.I., Konovalov A.I.

Reactivity of 4-phenyl-1,2,4-triazoline-3,5-dione and diethylazocarboxylate

in [4+2]-cycloaddition and ene reactions: solvent, temperature, and high-

pressure influence on the reaction rate // International journal of chemical

kinetics. — 2015. — V. 47. — P. 289‒301.

10. Kiselev V.D., Konovalov A.I. Internal and external factors

influencing the Diels-Alder reaction // Journal of physical organic

chemistry. — 2009. — V. 22. — P. 466‒483.
11. Kornilov D.A., Anikin O.V., Kolesnikova A.O., Bermeshev

M.V., Gubaidullin A.T., Kiselev V.D. Kinetics and thermochemistry of the
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