V. A. Khripach

Details der Publikationsliste

Zeitraum

1997 - 2007

Anzahl

22

Co-Autoren

Synthesis of [7,7-H-2(2)]epibrassinolide (2007)

Khripach, V.A., Khripach, N.B., Zhabinskii, V.N., Zhiburtovich, Y.Y., Schneider, B.

Synthesis of labelled epibrassinolide containing two deuterium atoms in a position which is not subjected to isotopic exchange is reported. Key transformations include preparation of 6,7-seco...

A new type of steroids with a cyclobutane fragment in the AB-ring moiety (2006)

Khripach, V.A., Zhabinskii, V.N., Fando, G.P., Kuchto, A.I., Khripach, N.B., Groen, M.B., ...

The synthesis of a 5,10-seco steroid containing two double bonds in a AB-macrocycle as well as the preparation of a steroidal skeleton with a cyclobutane fragment is described. The structures of...

Intramolecular cycloaddition/cycloreversion of (E)-3 beta,17 beta-diacetoxy-5,10-secoandrost-1(10)-en-5-one (2006)

Khripach, V.A., Zhabinskii, V.N., Kuchto, A.I., Zhiburtovich, Y.Y., Gromak, V.V., Groen, M.B., ...

Treatment of 3 beta,17 beta-diacetoxy-5,10-secoandrost-1(10)-en-5-one with (BF3Et2O)-Et-. was shown to proceed with cleavage of the macrocycle and formation of a new compound containing a...

Isolation and structure elucidation of new radical oxidation products of 5-hydroxy steroids (2006)

Khripach, V.A., Zhabinskii, V.N., Kuchto, A.I., Zhiburtovich, Y.Y., Lyakhov, A.S., Govorova, A.A., ...

Three new products have been isolated from the lead-tetraacetate version of the hypoiodite oxidation of 3 beta,17 beta-diacetoxy-5-hydroxy-5 alpha-androstane. Along with the expected 1(10)unsaturated...

The synthesis of functionalized 13,14-seco-steroids via Grob fragmentation (2004)

Khripach, V.A., Zhabinskii, V.N., Fando, G.P., Kuchto, A.I., Lyakhov, A.S., Govorova, A.A., ...

A synthetic methodology for the synthesis of 13,14-seco-steroids with substituents at C-14 and C-17 is described. The approach involves Grob fragmentation of 14-hydroxy-17-tosylates,...

Synthesis of 13,14-secotestosterone derivatives (2004)

Khripach, V.A., Zhabinskii, V.N., Kuchto, A.I., Zhiburtovich, Y.Y., Fando, G.P., Lyakhov, A.S., ...

A number of testosterone analogs with a 13,14-secosteroidal fragment have been prepared from (13S)-13-iodo-6-methoxy-3, 5-cyclo-13,14-seco-5-androstan-14,17-dione. The key steps involved...

Reaction of (13S)-13-iodo-6beta-methoxy-3alpha,5-cyclo-13,14-seco-5alpha-androstane-14,17-dione with hydroxylamine and its application to the synthesis of new 13,14-seco steroids (2004)

Khripach, V.A., Zhabinskii, V.N., Kuchto, A.I., Fando, G.P., Zhiburtovich, Y.Y., Lyakhov, A.S., ...

The synthesis of 13,14-seco steroids starting from easily available (13S)-13-iodo-6-methoxy-3,5-cyclo-13,14-seco-5-androsta-14,17-dione is described. The C-17 ketone was converted regioselectively...

Radical oxidation of 17-functionalized 14alpha-hydroxy steroids (2001)

Khripach, V.A., Zhabinskii, V.N., Kotyatkina, A.I., Fando, G.P., Zhiburtovich, Y.Y., Lyakhov, A.S., ...

The radical oxidation of 14a-hydroxy steroids with various functional groups at C-17 was studied. Lead tetraacetate and ceric ammonium nitrate were used as oxidizing agents. It was shown that...