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Collect. Czech. Chem. Commun. 1997, 62, 1325-1341
https://doi.org/10.1135/cccc19971325

Prostanoids: Synthesis of Enantiomers of 15-Deoxy-16-hydroxy-16-methylprostaglandin E1

Miroslav Terinek, Václav Kozmík and Jaroslav Paleček

Institute of Organic Chemistry, Prague Institute of Chemical Technology, 166 28 Prague 6,Czech Republic

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  • Ivanova N. A., Shavaleeva G. A., Spirikhin L. V., Miftakhov M. S.: Synthesis of a Misoprostol Analogue, 11-Deoxy-13,14-didehydro-17-methyl-20-norprostaglandin B1 Ethyl Ester. Russ J Org Chem 2024, 60, 1681. <https://doi.org/10.1134/S1070428024090094>
  • Kinoshita Akihiro, Higashino Masato, Yoshida Koji, Aratani Yoshiyuki, Kakuuchi Akito, Hanada Keisuke, Takeda Hiroyuki, Naganawa Atsushi, Matsuya Hidekazu, Ohmoto Kazuyuki: Synthesis and evaluation of a potent, well-balanced EP 2 /EP 3 dual agonist. Bioorganic & Medicinal Chemistry 2018, 26, 200. <https://doi.org/10.1016/j.bmc.2017.11.035>
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  • Vostrikov N. S., Loza V. V., Ivanova N. A., Miftakhov M. S.: Synthesis of ethyl (±)-(13,15-dideoxy)-16-methyl-9-oxoprosta-13(E,Z),15(E)-dienoate. Russ J Org Chem 2010, 46, 1301. <https://doi.org/10.1134/S107042801009006X>
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  • TERINEK M., KOZMIK V., PALECEK J.: ChemInform Abstract: Prostanoids: Synthesis of Enantiomers of 15‐Deoxy‐16‐hydroxy‐16‐ methylprostaglandin E1. ChemInform 1997, 28. <https://doi.org/10.1002/chin.199751266>