Reactivity of 17β-hydroxy-17α-substituted androstane derivatives

The work concerns the reactivity of 17β-hydroxy-17α-substituted androstanes 1-9. Depending on the nature of the 17α-substituent, the presence of the neighboring 16-oximino group, and the reagent used, these compounds can undergo retroaddition (10-12) and fragmentation-cyclization (14-16) reactio...

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Main Authors: Penov-Gaši Katarina M., Gaković Andrea R., Ajduković Jovana J., Đurendić-Brenesel Maja Đ., Đurendić Evgenija A., Savić Marina P., Sakač Marija N.
Format: Article
Language:English
Published: Faculty of Technology, Novi Sad 2010-01-01
Series:Acta Periodica Technologica
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/1450-7188/2010/1450-71881041169P.pdf
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spelling doaj-c0fd034d905944748b876ddc5325b42d2020-11-24T23:30:18ZengFaculty of Technology, Novi SadActa Periodica Technologica1450-71882010-01-0120104116917610.2298/APT1041169PReactivity of 17β-hydroxy-17α-substituted androstane derivativesPenov-Gaši Katarina M.Gaković Andrea R.Ajduković Jovana J.Đurendić-Brenesel Maja Đ.Đurendić Evgenija A.Savić Marina P.Sakač Marija N.The work concerns the reactivity of 17β-hydroxy-17α-substituted androstanes 1-9. Depending on the nature of the 17α-substituent, the presence of the neighboring 16-oximino group, and the reagent used, these compounds can undergo retroaddition (10-12) and fragmentation-cyclization (14-16) reactions. http://www.doiserbia.nb.rs/img/doi/1450-7188/2010/1450-71881041169P.pdfandrostane derivativesretroadditionfragmentationcyclization reaction
collection DOAJ
language English
format Article
sources DOAJ
author Penov-Gaši Katarina M.
Gaković Andrea R.
Ajduković Jovana J.
Đurendić-Brenesel Maja Đ.
Đurendić Evgenija A.
Savić Marina P.
Sakač Marija N.
spellingShingle Penov-Gaši Katarina M.
Gaković Andrea R.
Ajduković Jovana J.
Đurendić-Brenesel Maja Đ.
Đurendić Evgenija A.
Savić Marina P.
Sakač Marija N.
Reactivity of 17β-hydroxy-17α-substituted androstane derivatives
Acta Periodica Technologica
androstane derivatives
retroaddition
fragmentation
cyclization reaction
author_facet Penov-Gaši Katarina M.
Gaković Andrea R.
Ajduković Jovana J.
Đurendić-Brenesel Maja Đ.
Đurendić Evgenija A.
Savić Marina P.
Sakač Marija N.
author_sort Penov-Gaši Katarina M.
title Reactivity of 17β-hydroxy-17α-substituted androstane derivatives
title_short Reactivity of 17β-hydroxy-17α-substituted androstane derivatives
title_full Reactivity of 17β-hydroxy-17α-substituted androstane derivatives
title_fullStr Reactivity of 17β-hydroxy-17α-substituted androstane derivatives
title_full_unstemmed Reactivity of 17β-hydroxy-17α-substituted androstane derivatives
title_sort reactivity of 17β-hydroxy-17α-substituted androstane derivatives
publisher Faculty of Technology, Novi Sad
series Acta Periodica Technologica
issn 1450-7188
publishDate 2010-01-01
description The work concerns the reactivity of 17β-hydroxy-17α-substituted androstanes 1-9. Depending on the nature of the 17α-substituent, the presence of the neighboring 16-oximino group, and the reagent used, these compounds can undergo retroaddition (10-12) and fragmentation-cyclization (14-16) reactions.
topic androstane derivatives
retroaddition
fragmentation
cyclization reaction
url http://www.doiserbia.nb.rs/img/doi/1450-7188/2010/1450-71881041169P.pdf
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