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Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone

Liliya Khalitovna Faizullina 1
Liliya Khalitovna Faizullina
Yuliya Aleksandrovna Khalilova 1
Yuliya Aleksandrovna Khalilova
Farid Abdullovich Valeev 1
Farid Abdullovich Valeev
Published 2021-07-07
CommunicationVolume 31, Issue 4, 493-494
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Faizullina L. K., Khalilova Y. A., Valeev F. A. Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone // Mendeleev Communications. 2021. Vol. 31. No. 4. pp. 493-494.
GOST all authors (up to 50) Copy
Faizullina L. K., Khalilova Y. A., Valeev F. A. Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone // Mendeleev Communications. 2021. Vol. 31. No. 4. pp. 493-494.
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TY - JOUR
DO - 10.1016/j.mencom.2021.07.018
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.07.018
TI - Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone
T2 - Mendeleev Communications
AU - Faizullina, Liliya Khalitovna
AU - Khalilova, Yuliya Aleksandrovna
AU - Valeev, Farid Abdullovich
PY - 2021
DA - 2021/07/07
PB - Mendeleev Communications
SP - 493-494
IS - 4
VL - 31
ER -
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@article{2021_Faizullina,
author = {Liliya Khalitovna Faizullina and Yuliya Aleksandrovna Khalilova and Farid Abdullovich Valeev},
title = {Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone},
journal = {Mendeleev Communications},
year = {2021},
volume = {31},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.07.018},
number = {4},
pages = {493--494},
doi = {10.1016/j.mencom.2021.07.018}
}
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Faizullina, Liliya Khalitovna, et al. “Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone.” Mendeleev Communications, vol. 31, no. 4, Jul. 2021, pp. 493-494. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.07.018.

Abstract

Base-promoted intramolecular aldol condensation of diastereomeric Michael adducts of levoglucosenone and cyclododecanone affords 12-hydroxy-14,20-dioxatetra-cyclo[9.6.1.112,17.113,16]icosan-18-one as a mixture of three diastereomers. The products thus obtained are promising for synthesizing 14-membered macrocyclic compounds, including cembranoids and their analogues.

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