Literature DB >> 11720583

Novel synthetic approach to 19-nor-1alpha,25-dihydroxyvitamin D(3) and its derivatives by Suzuki-Miyaura coupling in solution and on solid support.

T Hanazawa1, T Wada, T Masuda, S Okamoto, F Sato.   

Abstract

19-nor-1alpha,25-Dihydroxyvitamin D(3) was synthesized by the Suzuki-Miyaura coupling of the A-ring intermediate 3, which was efficiently prepared from readily available 5-(tert-butyldimethylsilyl)oxycyclohex-2-enone (5), with the boronate compound of the C,D-ring portion. The method could be applied to a solid-phase synthesis to prepare the des-C,D derivatives of 19-nor-1alpha,25-dihydroxyvitamin D(3). [reaction: see text]

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Year:  2001        PMID: 11720583     DOI: 10.1021/ol016908r

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

Review 1.  Potent 19-norvitamin D analogs for prostate and liver cancer therapy.

Authors:  Atsushi Kittaka; Akihiro Yoshida; Kun-Chun Chiang; Masashi Takano; Daisuke Sawada; Toshiyuki Sakaki; Tai C Chen
Journal:  Future Med Chem       Date:  2012-10       Impact factor: 3.808

2.  Isotope effects and the mechanism of epoxidation of cyclohexenone with tert-butyl hydroperoxide.

Authors:  Chad F Christian; Tetsuya Takeya; Michael J Szymanski; Daniel A Singleton
Journal:  J Org Chem       Date:  2007-07-03       Impact factor: 4.354

3.  Novel vitamin d analogs for prostate cancer therapy.

Authors:  Tai C Chen; Atsushi Kittaka
Journal:  ISRN Urol       Date:  2011-09-19
  3 in total

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