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Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide

Mansur Sagar'yarovich Miftakhov 1
Mansur Sagar'yarovich Miftakhov
, 
Farid Abdullovich Valeev 1
Farid Abdullovich Valeev
, 
Irina Nikolaevna Gaisina 1
Irina Nikolaevna Gaisina
, 
Genrikh Alexandrovich Tolstikov 2
Genrikh Alexandrovich Tolstikov
10.1070/MC1994v004n02ABEH000341
Published 1994-04-30
Communication , Volume 4, Issue 2, 45-47
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Miftakhov M. S. et al. Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide // Mendeleev Communications. 1994. Vol. 4. No. 2. pp. 45-47.
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Miftakhov M. S., Valeev F. A., Gaisina I. N., Tolstikov G. A. Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide // Mendeleev Communications. 1994. Vol. 4. No. 2. pp. 45-47.
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TY - JOUR
DO - 10.1070/MC1994v004n02ABEH000341
UR - https://mendcomm.colab.ws/publications/10.1070/MC1994v004n02ABEH000341
TI - Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide
T2 - Mendeleev Communications
AU - Miftakhov, Mansur Sagar'yarovich
AU - Valeev, Farid Abdullovich
AU - Gaisina, Irina Nikolaevna
AU - Tolstikov, Genrikh Alexandrovich
PY - 1994
DA - 1994/04/30
PB - Mendeleev Communications
SP - 45-47
IS - 2
VL - 4
ER -
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@article{1994_Miftakhov,
author = {Mansur Sagar'yarovich Miftakhov and Farid Abdullovich Valeev and Irina Nikolaevna Gaisina and Genrikh Alexandrovich Tolstikov},
title = {Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide},
journal = {Mendeleev Communications},
year = {1994},
volume = {4},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1994v004n02ABEH000341},
number = {2},
pages = {45--47},
doi = {10.1070/MC1994v004n02ABEH000341}
}
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Miftakhov, Mansur Sagar'yarovich, et al. “Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide.” Mendeleev Communications, vol. 4, no. 2, Apr. 1994, pp. 45-47. https://mendcomm.colab.ws/publications/10.1070/MC1994v004n02ABEH000341.

Abstract

A series of schemes is described for the transformation of (−)-(lS,2S,3S,6R,7R,9R)-10,12-dioxatetracyclo[7.2.1.13,6-02,7]- tridecan-8-one, prepared via hydrogenation of a Diels–Alder adduct of levoglucosenone and cyclopentadiene, into key products (+)-(1 R,2R,5RS,7S,8S)- and (−)-(1S,2S,5RS,7R,8R)-4-oxatricyclo[6.1.2.02,7]undecan-5-ols and subsequently into the title compounds.

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