| Literature DB >> 35476519 |
Jieyu Gu1, Kevin X Rodriguez1, Yuzuru Kanda1, Shenghua Yang1, Michal Ociepa1, Henrik Wilke1, Arteen V Abrishami1, Lars Jørgensen2, Tine Skak-Nielsen2, Jason S Chen1, Phil S Baran1.
Abstract
A convergent approach for the total synthesis of calcipotriol (brand name: Dovonex), a proven vitamin D analog used for the treatment of psoriasis, and medicinally relevant synthetic analogs is described. A complete approach, not wedded to semisynthesis, toward both the A-ring and CD-ring is reported. From a retrosynthetic standpoint, hidden symmetry within the decorated A-ring is disclosed, which allowed for scalable quantities of this advanced intermediate. In addition, a radical retrosynthetic approach is described, which highlights an electrochemical reductive coupling as well as an intramolecular hydrogen atom transfer Giese addition to establish the 6,5-transcarbon skeleton found in the vitamin D family. Finally, a late-stage decarboxylative cross-coupling approach allowed for the facile preparation of various C20-arylated derivatives that show promising biological activity in an initial bioassay.Entities:
Keywords: electrosynthesis; medicinal chemistry; radical retrosynthesis; total synthesis; vitamin D
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Substances:
Year: 2022 PMID: 35476519 PMCID: PMC9170165 DOI: 10.1073/pnas.2200814119
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 12.779