Synthesis and reactions of malonic esters based on hydroxymethyl-1,3-dioxacycloalkanes
Тип публикации: Journal Article
Дата публикации: 2025-02-01
SCImago Q3
БС2
SJR: 0.272
CiteScore: 2.8
Impact factor: 1.7
ISSN: 10665285, 15739171
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Malonates bearing 1,3-dioxacycloakane moiety were synthesized and some of their reactions were carried out under conditions of conventional heating and microwave irradiation. New malonates can be successfully used as C—H acids in the alkylation reaction as well as for the synthesis of tertiary amines and olefins. The conditions for synthesizing target products in quantitative yields using microwave activation were developed.
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Borisova Yu. G. et al. Synthesis and reactions of malonic esters based on hydroxymethyl-1,3-dioxacycloalkanes // Russian Chemical Bulletin. 2025. Vol. 74. No. 2. pp. 428-433.
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Borisova Yu. G., Sultanova R. M., Zlotsky S. S. Synthesis and reactions of malonic esters based on hydroxymethyl-1,3-dioxacycloalkanes // Russian Chemical Bulletin. 2025. Vol. 74. No. 2. pp. 428-433.
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TY - JOUR
DO - 10.1007/s11172-025-4534-5
UR - https://link.springer.com/10.1007/s11172-025-4534-5
TI - Synthesis and reactions of malonic esters based on hydroxymethyl-1,3-dioxacycloalkanes
T2 - Russian Chemical Bulletin
AU - Borisova, Yu G
AU - Sultanova, R M
AU - Zlotsky, S. S.
PY - 2025
DA - 2025/02/01
PB - Springer Nature
SP - 428-433
IS - 2
VL - 74
SN - 1066-5285
SN - 1573-9171
ER -
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@article{2025_Borisova,
author = {Yu G Borisova and R M Sultanova and S. S. Zlotsky},
title = {Synthesis and reactions of malonic esters based on hydroxymethyl-1,3-dioxacycloalkanes},
journal = {Russian Chemical Bulletin},
year = {2025},
volume = {74},
publisher = {Springer Nature},
month = {feb},
url = {https://link.springer.com/10.1007/s11172-025-4534-5},
number = {2},
pages = {428--433},
doi = {10.1007/s11172-025-4534-5}
}
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Borisova, Yu. G., et al. “Synthesis and reactions of malonic esters based on hydroxymethyl-1,3-dioxacycloalkanes.” Russian Chemical Bulletin, vol. 74, no. 2, Feb. 2025, pp. 428-433. https://link.springer.com/10.1007/s11172-025-4534-5.
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