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13C-NMR study of 4-azasteroids in solution and solid state

Steroids, 2002
Jacek W Morzycki   +2 more
exaly   +2 more sources

Recent advances in azasteroids chemistry.

Steroids, 2008
Modified steroids have attracted a great deal of attention these last years. Their preparation is a stimulating challenge to the organic chemist, often demanding development of new and generally useful reactions. Moreover, the biological properties of modified steroids have proved to be of interest.
Malika Ibrahim-ouali, L. Rocheblave
semanticscholar   +3 more sources

N-Alkylation of 17-azasteroids

Steroids, 1994
N-Alkylation of 17-azasteroid lactams (16-oxo-17-azaandrost-5-en-3 beta-ol acetate 3 and its D-homo analog 4) was studied. It has been found that both lactams are readily alkylated with iodomethane or iodoethane. In contrast to this there was no reaction with 2-iodo-6-methylheptane due to the steric hindrance.
Jacek W Morzycki
exaly   +3 more sources

Phosphorescence of 8-azasteroids and related compounds

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2005
We have investigated the electron absorption, fluorescence and phosphorescence spectra of 8-azasteroids and model compounds containing enaminodicarbonyl fragment. It has been shown that the investigated compounds have absorption and phosphorescence spectra similar in form and position.
S A Bagnich
exaly   +3 more sources

Azasteroids from diosgenin: Synthesis and evaluation of their antiproliferative activity.

Steroids, 2020
In this work, we report the synthesis of two new azasteroids through the modification of the A and B rings of diosgenin 1. The 4-azasteroid derivative 12 was prepared in three steps using the α,β-insaturated-3-keto compound 11 as a precursor, which was ...
Anselmo A. Martínez-Gallegos   +5 more
semanticscholar   +1 more source

ChemInform Abstract: AZASTEROIDE 1. MITT. SYNTH. EINES AZASTEROID‐RINGSYST.

Chemischer Informationsdienst. Organische Chemie, 1970
AbstractBeim Erhitzen von 2‐(1‐Cyclohexenyl)‐ähhylamin (I) mit dem Ester (II) am Rückfluß entsteht das Enaminlactam (III) (als Doppelbindungsisomerengemisch) in einer Ausbeute von 86%.
S. OHKI, M. AKIBA
openaire   +1 more source

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