6-Chloro-and 6-bromo-substituted steroids in the Suzuki-Miyaura cross-coupling reaction. A convenient route to potential aromatase inhibitors
…, PA Donez, GA Skryabin, IP Beletskaya
Index: Lukashev, Nikolay V.; Latyshev, Gennadij V.; Donez, Pavel A.; Skryabin, George A.; Beletskaya, Irina P. Synthesis, 2006 , # 3 p. 533 - 539
Full Text: HTML
Citation Number: 11
Abstract
Abstract Chlorine at an sp 2-carbon in steroids has been shown to be reactive in Suzuki- Miyaura cross-coupling reactions with either Ni or Pd catalysts. The coupling of analogous 6- bromo derivatives has also been demonstrated to be applicable to a wider scope of substrates. The Suzuki-Miyaura arylation of 6-bromo-Δ 3, 5-steroid enol ethers with subsequent hydrolysis is a useful route to 6-arylated steroids bearing aryl at a saturated ...
Related Articles:
Aromatase inhibitors. Synthesis and biological activity of androstenedione derivatives
[Marsh, David A.; Brodie, Harry J.; Garrett, Wesley; Tsai-Morris, Chon-Hwa; Brodie, Angela M. H. Journal of Medicinal Chemistry, 1985 , vol. 28, # 6 p. 788 - 795]