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Collect. Czech. Chem. Commun. 1998, 63, 1564-1574
https://doi.org/10.1135/cccc19981564

Synthesis of 17β-Isoxazolyl Steroids and Spiro[steroid-17,2'-furanone]s

Alexander V. Baranovskya, Marinus B. Groenb, Aede de Grootc, Raissa P. Litvinovskayaa and Vladimir A. Khripacha

a Institute of Bioorganic Chemistry, National Academy of Sciences, Zhodinskaya str. 5/2, 220141 Minsk, Belarus
b Scientific Development Group, N. V. Organon, P.O. Box 20, 5340 BH Oss, The Netherlands
c Laboratory of Organic Chemistry, Agricultural University, Dreijenplein 8, 6703 HB Wageningen, The Netherlands

Crossref Cited-by Linking

  • Baranovsky Alexander, Ladyko Alesya, Shkel Tatsiana, Sokolov Sergey, Strushkevich Natallia, Gilep Andrey: Transformations, NMR studies and biological testing of some 17β-isoxazolyl steroids and their heterocyclic ring cleavage derivatives. Steroids 2021, 166, 108768. <https://doi.org/10.1016/j.steroids.2020.108768>
  • Burghart‐Stoll Heike, Brückner Reinhard: Total Syntheses of the Gregatins A–D and Aspertetronin A: Structure Revisions of These Compounds and of Aspertetronin B, Together with Plausible Structure Revisions of Gregatin E, Cyclogregatin, Graminin A, the Penicilliols A and B, and the Huaspenones A and B. Eur J Org Chem 2012, 2012, 3978. <https://doi.org/10.1002/ejoc.201200207>
  • Kato Keisuke, Nouchi Hideaki, Ishikura Keisuke, Takaishi Satoshi, Motodate Satoshi, Tanaka Hikaru, Okudaira Kazuho, Mochida Tomoyuki, Nishigaki Ryuichiro, Shigenobu Koki, Akita Hiroyuki: A facile access to spiro furanone skeleton based on Pd(II)-mediated cyclization–carbonylation of propargylic esters. Tetrahedron 2006, 62, 2545. <https://doi.org/10.1016/j.tet.2005.12.033>