Publication date: Available online 18 July 2017
Source:The Journal of Steroid Biochemistry and Molecular Biology
Author(s): Rita Sigüeiro, Patricia González-Berdullas, Julian Loureiro, Antonio Mouriño, Miguel A. Maestro
A convergent approach to 25S,26-dihydroxyvitamin D3 (1) has been developed in our laboratories. The A-ring and the CD-fragment are constructed from ergocalciferol and Inhoffen-Lythgoe diol, respectively. The triene system is assembled by a Wittig-Horner coupling. With this convergent synthesis, a novel hydroxylated vitamin D metabolite in our laboratory is available for biological testing.
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Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00302841026182,00306932607174,alsfakia@gmail.com,
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Τετάρτη 19 Ιουλίου 2017
Stereoselective synthesis of 25S,26-dihydroxyvitamin D3
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