Stereocontrolled synthesis of the four 16-hydroxymethyl-19-nortestosterone isomers and their antiproliferative activities
Abstract Novel 16-hydroxymethyl-19-nortestosterone diastereomers were prepared by Birch reduction from the corresponding 3-methoxy-16-hydroxymethylestra-1,3,5(10)-trien-17-ol isomers with known configurations. The synthetized compounds are 16α- and 16β-hydroxymethyl-substituted 19-nortestosterone an...
Elmentve itt :
Szerzők: |
Schneider Gyula Kiss Anita Mernyák Erzsébet Benke Zsanett Amália Wölfling János Nagyné Frank Éva Bózsity Noémi Gyovai András Minorics Renáta Zupkó István |
---|---|
Dokumentumtípus: | Cikk |
Megjelent: |
2016
|
Sorozat: | STEROIDS
105 |
doi: | 10.1016/j.steroids.2015.12.003 |
mtmt: | 2982886 |
Online Access: | http://publicatio.bibl.u-szeged.hu/6918 |
Hasonló tételek
-
Stereoselective synthesis of the four 16-hydroxymethyl-3-methoxy- and 16- hydroxymethyl-3-benzyloxy-13α-estra-1,3,5(10)-trien-17-ol isomers and their antiproliferative activities
Szerző: Kiss Anita, et al.
Megjelent: (2018) -
Stereocontrolled synthesis of the four possible 3-methoxy and 3-benzyloxy-16-triazolyl-methyl-estra-17-ol hybrids and their antiproliferative activities
Szerző: Kiss Anita, et al.
Megjelent: (2019) -
Antiproliferative properties of newly synthesized 19-nortestosterone analogs without substantial androgenic activity
Szerző: Gyovai András, et al.
Megjelent: (2018) -
Improved stereoselective synthesis of 3-methoxy- and 3-benzyloxy-16-hydroxymethyl-13α-estra-1,3,5(10)-trien-17-ol isomers by transfer hydrogenation using chiral Ru catalysts
Szerző: Kiss Anita, et al.
Megjelent: (2018) -
Synthesis and biological evaluation of 13α-estrone derivatives as potential antiproliferative agents
Szerző: Szabó Johanna, et al.
Megjelent: (2016)