Research output: Contribution to journal › Review article › peer-review
Squaramide-Based Catalysts in Organic Synthesis (A Review). / Popova, E. A.; Pronina, Yu A.; Davtian, A. V.; Nepochatyi, G. D.; Petrov, M. L.; Boitsov, V. M.; Stepakov, A. V.
In: Russian Journal of General Chemistry, Vol. 92, No. 3, 03.2022, p. 287-347.Research output: Contribution to journal › Review article › peer-review
}
TY - JOUR
T1 - Squaramide-Based Catalysts in Organic Synthesis (A Review)
AU - Popova, E. A.
AU - Pronina, Yu A.
AU - Davtian, A. V.
AU - Nepochatyi, G. D.
AU - Petrov, M. L.
AU - Boitsov, V. M.
AU - Stepakov, A. V.
N1 - Publisher Copyright: © 2022, Pleiades Publishing, Ltd.
PY - 2022/3
Y1 - 2022/3
N2 - Abstract: The review considers works published over the past 5 years on the synthesis, modifications, and application of chiral catalysts based on squaramides in organic synthesis. The data are grouped by types of reactions catalyzed by squaramide organocatalysts: Michael, Mannich, Pictet–Spengler, Friedel–Crafts, Henry reactions, aldol condensation, cycloaddition. For each reaction, a mechanism is considered that demonstrates the catalytic effect of squaramide organocatalysts.
AB - Abstract: The review considers works published over the past 5 years on the synthesis, modifications, and application of chiral catalysts based on squaramides in organic synthesis. The data are grouped by types of reactions catalyzed by squaramide organocatalysts: Michael, Mannich, Pictet–Spengler, Friedel–Crafts, Henry reactions, aldol condensation, cycloaddition. For each reaction, a mechanism is considered that demonstrates the catalytic effect of squaramide organocatalysts.
KW - chiral squaramides
KW - cycloaddition reactions
KW - enantioselective organocatalysis
KW - Friedel–Crafts reaction
KW - Henry reaction
KW - Mannich reaction
KW - organic synthesis
KW - Pictet–Spengler reaction
UR - http://www.scopus.com/inward/record.url?scp=85128112825&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/eecfc22b-d2a8-3c39-ac9a-689655959bca/
U2 - 10.1134/s107036322203001x
DO - 10.1134/s107036322203001x
M3 - Review article
AN - SCOPUS:85128112825
VL - 92
SP - 287
EP - 347
JO - Russian Journal of General Chemistry
JF - Russian Journal of General Chemistry
SN - 1070-3632
IS - 3
ER -
ID: 100063038