Pd-catalyzed synthesis of 2-alkynyl derivatives of 19β,28-epoxy-18α-olean-1-en-3-one
- Authors: Shakhmaev R.N.1, Sunagatullina A.S.1, Abdullina E.A.1, Zorin V.V.1
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Affiliations:
- Ufa State Petroleum Technological University
- Issue: Vol 53, No 11 (2017)
- Pages: 1705-1709
- Section: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/216957
- DOI: https://doi.org/10.1134/S1070428017110173
- ID: 216957
Cite item
Abstract
Basing on Sonogashira reaction of 2-iodo-19β,28-epoxy-18α-olean-1-en-3-one with alkynes an effective approach was developed to the synthesis of 2-alkynyl derivatives of 19β,28-epoxy-18α-olean-1-en-3-one. Initial 2-iodo-19β,28-epoxy-18α-olean-1-en-3-one was obtained by isomerization of the accessible betulin into allobetulin in the presence of Amberlyst 15, oxidation of allobetulin to 19β,28-epoxy-18α-olean-1-en-3-one under the action of 2-iodoxybenzoic acid, and iodination of the obtained enone in the presence of DMAP.
About the authors
R. N. Shakhmaev
Ufa State Petroleum Technological University
Email: biochem@rusoil.net
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
A. Sh. Sunagatullina
Ufa State Petroleum Technological University
Email: biochem@rusoil.net
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
E. A. Abdullina
Ufa State Petroleum Technological University
Email: biochem@rusoil.net
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
V. V. Zorin
Ufa State Petroleum Technological University
Author for correspondence.
Email: biochem@rusoil.net
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
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