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A short synthesis of the carbocyclic core of Entecavir from Corey lactone

Zuleykha Rakhim'yanovna Valiullina 1
Zuleykha Rakhim'yanovna Valiullina
, 
Vera Anatol'evna Akhmet'yanova 1
Vera Anatol'evna Akhmet'yanova
, 
Nikolay Sergeyevich Vostrikov 1
Nikolay Sergeyevich Vostrikov
, 
Mansur Sagar'yarovich Miftakhov 1
Mansur Sagar'yarovich Miftakhov
10.1016/j.mencom.2016.01.004
Published 2015-12-30
Communication , Volume 26, Issue 1, 9-10
7
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Valiullina Z. R. et al. A short synthesis of the carbocyclic core of Entecavir from Corey lactone // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 9-10.
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Valiullina Z. R., Akhmet'yanova V. A., Vostrikov N. S., Miftakhov M. S. A short synthesis of the carbocyclic core of Entecavir from Corey lactone // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 9-10.
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TY - JOUR
DO - 10.1016/j.mencom.2016.01.004
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.004
TI - A short synthesis of the carbocyclic core of Entecavir from Corey lactone
T2 - Mendeleev Communications
AU - Valiullina, Zuleykha Rakhim'yanovna
AU - Akhmet'yanova, Vera Anatol'evna
AU - Vostrikov, Nikolay Sergeyevich
AU - Miftakhov, Mansur Sagar'yarovich
PY - 2015
DA - 2015/12/30
PB - Mendeleev Communications
SP - 9-10
IS - 1
VL - 26
ER -
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@article{2015_Valiullina,
author = {Zuleykha Rakhim'yanovna Valiullina and Vera Anatol'evna Akhmet'yanova and Nikolay Sergeyevich Vostrikov and Mansur Sagar'yarovich Miftakhov},
title = {A short synthesis of the carbocyclic core of Entecavir from Corey lactone},
journal = {Mendeleev Communications},
year = {2015},
volume = {26},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.004},
number = {1},
pages = {9--10},
doi = {10.1016/j.mencom.2016.01.004}
}
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Valiullina, Zuleykha Rakhim'yanovna, et al. “A short synthesis of the carbocyclic core of Entecavir from Corey lactone.” Mendeleev Communications, vol. 26, no. 1, Dec. 2015, pp. 9-10. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.004.

Abstract

The readily available Corey lactone was converted in three simple stages to tris-TBS-ether of (1R*,3R*,5S*)-1-hydroxymethyl-3,5-dihydroxy-2-methylidenecyclopentane – the protected carbocyclic core of Entecavir, one of the best medicines against hepatitis.

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