Synthesis of Ethyl Ester of 11-Deoxy-13,14-didehydro-17-methyl-20-norprostaglandin B1_Analog of Misoprostol

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Abstract

By 1,2-addition to the keto group ethyl-(5-oxocyclopent-1-enyl)heptenoate lithium acetylenide from 4-hydroxy-4,5-dimethylheptin-1, followed by oxidative isomerization of the resulting adduct with PCC was obtained ethyl ester 11-deoxy-13,14-didehydro-17-methyl-20-nor-prostaglandin B1.

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N. A. Ivanova

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)

Author for correspondence.
Email: gushavaleeva@mail.ru
ORCID iD: 0000-0002-3101-1285
Russian Federation, prosp. Oktabrya, 71, Ufa, 450054

G. A. Shavaleeva

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)

Email: gushavaleeva@mail.ru
ORCID iD: 0000-0003-1345-9139
Russian Federation, prosp. Oktabrya, 71, Ufa, 450054

L. V. Spirikhin

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)

Email: gushavaleeva@mail.ru
ORCID iD: 0000-0002-3163-882X
Russian Federation, prosp. Oktabrya, 71, Ufa, 450054

M. S. Miftakhov

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)

Email: gushavaleeva@mail.ru
ORCID iD: 0000-0002-0269-7484
Russian Federation, prosp. Oktabrya, 71, Ufa, 450054

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