Pd-catalyzed synthesis of 2-alkynyl derivatives of 19β,28-epoxy-18α-olean-1-en-3-one


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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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