Published February 2019 | Version v1
Journal article

14β-(Isoxazol-3-yl)methylestrane Steroids: Chemoselective Synthesis and Transformations with Heterocyclic Ring Opening

  • 1. National Academy of Sciences of Belarus, Institute of Bioorganic Chemistry (Belarus)
  • 2. Blokhin National Medical Research Center of Oncology (Russian Federation)

Description

Steroids containing an isoxazole, isoxazoline, or enaminocarbonyl substituent at C-14 and a C-14-C-15-fused pyrrolidine ring were synthesized. The influence of solvents on the result of dipolar cycloaddition and solvolysis of bridged nitrosteroids was evaluated. Cytotoxicity testing of estrone analogs on cancer cells of various origins revealed activity against breast, colorectal, prostate, and lung cancer cells.

Additional details

Identifiers

Publishing Information

Journal Title
Russian Journal of Organic Chemistry
Journal Volume
55
Journal Issue
2
Journal Page Range
p. 202-214
ISSN
1070-4280

Optional Information

Copyright
Copyright (c) 2019 Pleiades Publishing, Ltd.