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A New Approach to the Synthesis of 15-A2tIsoP Isoprostane and 14-A4tNeuroP Neuroprostane

Vladimir Vsevolodovich Veselovsky 1
Vladimir Vsevolodovich Veselovsky
, 
Antonina Vasil'evna Lozanova 1
Antonina Vasil'evna Lozanova
, 
Andrei Valentinovich Stepanov 1
Andrei Valentinovich Stepanov
10.1016/j.mencom.2012.09.008
Published 2012-09-17
Communication , Volume 22, Issue 5, 252-253
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Veselovsky V. V., Lozanova A. V., Stepanov A. V. A New Approach to the Synthesis of 15-A2tIsoP Isoprostane and 14-A4tNeuroP Neuroprostane // Mendeleev Communications. 2012. Vol. 22. No. 5. pp. 252-253.
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Veselovsky V. V., Lozanova A. V., Stepanov A. V. A New Approach to the Synthesis of 15-A2tIsoP Isoprostane and 14-A4tNeuroP Neuroprostane // Mendeleev Communications. 2012. Vol. 22. No. 5. pp. 252-253.
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TY - JOUR
DO - 10.1016/j.mencom.2012.09.008
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.09.008
TI - A New Approach to the Synthesis of 15-A2tIsoP Isoprostane and 14-A4tNeuroP Neuroprostane
T2 - Mendeleev Communications
AU - Veselovsky, Vladimir Vsevolodovich
AU - Lozanova, Antonina Vasil'evna
AU - Stepanov, Andrei Valentinovich
PY - 2012
DA - 2012/09/17
PB - Mendeleev Communications
SP - 252-253
IS - 5
VL - 22
ER -
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@article{2012_Veselovsky,
author = {Vladimir Vsevolodovich Veselovsky and Antonina Vasil'evna Lozanova and Andrei Valentinovich Stepanov},
title = {A New Approach to the Synthesis of 15-A2tIsoP Isoprostane and 14-A4tNeuroP Neuroprostane},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.09.008},
number = {5},
pages = {252--253},
doi = {10.1016/j.mencom.2012.09.008}
}
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Veselovsky, Vladimir Vsevolodovich, et al. “A New Approach to the Synthesis of 15-A2tIsoP Isoprostane and 14-A4tNeuroP Neuroprostane.” Mendeleev Communications, vol. 22, no. 5, Sep. 2012, pp. 252-253. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.09.008.

Abstract

A formal synthesis of the title natural cyclopentanoids was implemented based on intramolecular [3 + 2] cycloaddition in unsaturated silyl nitronates at the key step.

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